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    <title>START Center for Cancer Research Jobs</title>
    <link>https://ejob.bz/CompanyPortal.do?companyGK=51234&amp;portalGK=41776</link>
    <description><![CDATA[Job Postings available for application.]]></description>
    <language>en-us</language>
    <pubDate>Thu, 09 Apr 2026 01:57:20 EDT</pubDate>
    <lastBuildDate>Thu, 09 Apr 2026 01:57:20 EDT</lastBuildDate>
    <generator>BrightMove ATS</generator>
    <item>
      <title><![CDATA[Patient Care Technician - San Antonio, TX]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27775056&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>42eb2e6b-5309-496e-bc35-9a67987b697a</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering "Hope Through Access&rdquo; to cutting edge trials throughout the United States and Europe.  
 We are seeking a Patient Care Technician. The Patient Care Technician is responsible for providing patient care to individuals who are participants in clinical trials that are conducted at START. The PCT uses appropriate judgment and decision-making in planning and providing care. Care is to be delivered in a manner consistent with the Standard Operating Procedures and standards of practice, and professional evidence-based standards.
Work Schedule: 7:45am-4:30pm M-F
Location: San Antonio, TX
Essential Responsibilities:

Assist professional nurses and/or physicians in conducting examinations.
Perform ECGs.
Discuss patients' condition with nursing team.
Draw blood obtaining specimens for clinical labs and research labs.
Take vital signs.
Prepare patients for examinations, tests and treatments and explain procedures.
Record necessary information for review by nurses or physicians.
May assist with clinical research or perform other specialized duties requiring supplemental training.
Inventory and requisition of supplies and instruments.
Set up equipment and prepare medical exam rooms.
Prepare charts and lab requisitions for the next clinic day.

Education & Experience

High School Diploma or GED.
Current BLS certification.

Preferred Experience

1 year of experience.
Previous oncology and/or clinical trials experience.  

Best-in-Class Benefits and Perks 
We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package&mdash;based on experience&mdash;along with comprehensive benefits designed to support you both personally and professionally:  

401(k) retirement savings plan with employer match 
Eligibility for an annual performance bonus, based on role and company results 
Generous paid time off and paid holidays 
Comprehensive medical, dental, and vision coverage and optional insurance options 
Companypaid life and disability insurance for added financial protection 
Employee Assistance Program (EAP) providing confidential, nocost support for you and your family from day one 
Flexible FSA and HSA plans to support your financial wellness 
Commitment to a supportive environment that values balance, wellbeing, and flexibility 
We&rsquo;re committed to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START, you&rsquo;ll join a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation. 

More About START 
START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. START represents the world&rsquo;s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of &ldquo;Hope Through Access&rdquo;. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash; one of the most effective cancer drugs in medical history. 
 Learn more atSTARTresearch.com.  
 Ready to be part of a team changing the future of cancer treatment? 
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online. 
 We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Wed, 08 Apr 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Pre-Award Coordinator - San Antonio, TX]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27774904&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>9f702530-db67-41e8-aa34-c8131a33867c</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. To date, over 45 therapies conducted at START locations have obtained FDA/EMA approval. 
The START Center for Cancer Research is seeking a Pre-Award Coordinator who will be dedicated to connecting with Sponsors, CROs, sites, and key opinion leaders to advance clinical trials in the best way. In addition, this role is responsible for maintaining new study proposals in response to requests from prospective customers. 
This is a remote role. The annual base salary for this role is $55,000 - $65,000. However, base pay may vary depending on multiple individualized factors including market location, job-related knowledge, skills, and experience. 
Essential Responsibilities

Perform all pre-award activities from time of initial contact to official site selection for the START Network sites.
Review, respond, and maintain the central email inbox for new study opportunities.
Facilitate all pre-award related meetings, including but not limited to, Protocol Review and Development Committee meetings, Pre-Study Site Visits, weekly Study Start-Up Status meetings, and Sponsor/Investigator meetings for the START Europe sites.
Coordinate facility tours prior to official site selection.
Support execution of the Sponsor/CRO required site feasibility questionnaires for the START Network sites when applicable and ensuring the questionnaire are completed accurately and in a timely manner.
Work within the forecasted timelines in accordance with Sponsor/CRO expectations and ensure they are met; if forecasted timelines are not reached, provide clear rationale for delays and contingency plans to mitigate impact.
Review and comply with Standard Operating Procedures and pre-award processes in a timely manner and ensure all relevant documents are submitted to Sponsor/CRO and the Investigational Site File (ISF).
Anticipate and identify issues during pre-award process, resolve minor to moderate issues independently, and escalate complex issues.
Maintain and ensure data tracking systems are updated with pre-award milestones.
Assist with in-service trainings and new hire trainings for staff.
Assist with special projects as assigned.  This includes, but is not limited to, conducting research, preparing presentations and documents as requested.

Required Education and Experience: 

High school diploma or equivalent.
At least two years&rsquo; experience in administrative setting Proficient working knowledge of word processing, spreadsheet, database, and presentation software (MS Office skills such as Outlook, Word, Excel, PowerPoint, and SharePoint)
Excellent written and oral communication skills, as well as time management skills
Demonstrated ability to work in a dynamic environment under compressed deadlines across several projects, each with unique requirements.

Preferred Education and Experience: 

Experience in clinical research (monitoring, Feasibility/Study Start-Up experience).
Understanding of medical terminology.

Physical & Travel Requirements: 

Ability to sit at a desk or workstation for extended periods.
Ability to perform occasional walking (e.g., to retrieve documents, attend meetings) or light physical activity as necessary.
Ability to perform repetitive tasks involving typing, clicking, and scrolling.
Ability to read, comprehend, and respond to digital communications (e.g., emails, chat messages, documents) on a computer screen for extended periods.

Best-in-Class Benefits and Perks
We value our employees&rsquo; time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:

Comprehensive health coverage: Medical, dental, and vision insurance provided
Robust retirement planning: 401(k) plan available with employer matching
Financial security: Life and disability insurance for added protection
Flexible financial options: Health savings and flexible spending accounts offered
Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided
Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.

More about The START Center for Cancer Research
Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including for 43 therapies that were approved by the FDA. START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. Learn more at STARTresearch.com.
Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.
We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Mon, 06 Apr 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Clinical Data Entry Coordinator - West Valley City, UT]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27774615&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>25da45c5-f7fc-486b-b145-cd2276570f69</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. To date, over 45 therapies conducted at START locations have obtained FDA/EMA approval. 
The START Center for Cancer Research is seeking a Clinical Data Entry Coordinator who will collect, enter/transcribe, and transmit/submit clinical data for assigned investigational drug studies. 
Essential Responsibilities

Collect, enter/transcribe, and transmit/submit clinical data in paper and/or electronic case report forms (CRFs), including correction and query resolution for assigned investigational drug studies.  
Receive and request patient records/data from the study team as required to complete CRFs for assigned studies.   
Review patient data for completeness and accuracy for assigned studies. 
Coordinate and schedule monitor visits for assigned studies.  This includes exit meetings with monitors to review data or queries. 
Identify lab facilities used for assigned studies and communicate to the Regulatory Affairs staff so that lab certifications can be requested for the study file. 
Review and utilize protocols as guides for study activities for assigned studies.  
Assure that data entry remains current for all assigned studies.  
Attend meetings as required for assigned studies.  This includes, but is not limited to, site initiation meetings, monitor exit meetings, close-out visit meetings, and audit preparation meetings.  
Be available and on-site, if required, during audits for assigned studies.  
Communicate as needed with accounts receivable staff regarding submitted data.  

Required Education and Experience: 

Bachelor&rsquo;s degree or equivalent experience in lieu of degree.   
Knowledge and training in general office administration skills, including computer applications, filing systems, etc.

Preferred Education and Experience: 

Ability to accurately perform data review and CRF completion in its entirety with minimal direction.   
Familiarity with medical terminology. 
Additional demonstration of clinical research knowledge as evidenced by the use of either CCRP or CCRC credentials is highly desirable.   

Physical & Travel Requirements: 

Travel required up to 10% of the time. 
Sitting for extended periods of time. 
Typing and computer use for extended periods of time. 

Best-in-Class Benefits and Perks
We value our employees&rsquo; time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:

Comprehensive health coverage: Medical, dental, and vision insurance provided
Robust retirement planning: 401(k) plan available with employer matching
Financial security: Life and disability insurance for added protection
Flexible financial options: Health savings and flexible spending accounts offered
Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided
Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.

More about The START Center for Cancer Research
Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including for 43 therapies that were approved by the FDA. START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. Learn more at STARTresearch.com.
Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.
We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Tue, 31 Mar 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[CTMS Entry Coordinator - San Antonio, TX]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27774482&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>de6c8b9d-61b7-4c26-97b5-c72f0dd64453</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering "Hope Through Access&rdquo; to cutting edge trials throughout the United States and Europe.  
 We are seeking a CTMS Entry Coordinator.  This role will assist the Clinical Research Coordinators in all tasks to support their roles. It will require an understanding of research terminology and basic protocol interpretation.
Work Schedule: Monday-Friday, 8am-5pm
Location: 4383 Medical Dr, San Antonio, TX 78229
Essential Responsibilities

Collect, de-identify, enter/transcribe, and transmit/submit clinical data in paper and/or electronic case reports forms (CRFs), including correction and query resolution for assigned investigational drug studies. This includes but is not limited to images, lab results, and ECGs. 
Collaborate with Clinical Research Coordinator to ensure data timepoints are accurate and provide query resolution.
Contact patients in follow-up as needed per protocol.
Review and utilize protocols as guides for study activities for assigned studies.
Assist with the setup and formatting of study-specific Eligibility, Study Schedules, and Flow Sheets documents per protocol.
Assist with CTMS upkeep, including but not limited to tracking patient visits, IRB re-consents, Serious Adverse Events (SAEs) and Deviations.
Ensure that data transmissions remain current for assigned studies.
Provide support and information to onsite and remote monitors as necessary.
Comply with all applicable regulations, guidelines, and procedures pertaining to data loading, EDC systems, and clinical research.
Share responsibility with Data Coordinators to identify lab facilities and normal lab values used for assigned studies so that lab certifications can be requested for the study file.
Attend meetings regarding assigned studies as needed, including site initiation visits, Roster meetings and Forms Committee.
Communicate as needed with accounts receivable staff regarding transmitted data.
Other duties may be assigned at any time.

 Required Education and Experience:

High School diploma or equivalent.
One year of research administrative experience within a healthcare, pharmaceutical, or research organization.
Knowledge and training in general office administration skills, including computer applications, filing systems, etc. 
Familiarity with medical terminology.
Strong organizational skills and a sense of timeliness in completing projects.
Must be detail-oriented and able to understand instructions and work independently. 

 Best-in-Class Benefits and Perks 
We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package&mdash;based on experience&mdash;along with comprehensive benefits designed to support you both personally and professionally:   

401(k) retirement savings plan with employer match 
Eligibility for an annual performance bonus, based on role and company results 
Generous paid time off and paid holidays 
Comprehensive medical, dental, and vision coverage and optional insurance options 
Companypaid life and disability insurance for added financial protection 
Employee Assistance Program (EAP) providing confidential, nocost support for you and your family from day one 
Flexible FSA and HSA plans to support your financial wellness 
Commitment to a supportive environment that values balance, wellbeing, and flexibility 
We&rsquo;re committed to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START, you&rsquo;ll join a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation. 

 More About START 
START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. START represents the world&rsquo;s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of &ldquo;Hope Through Access&rdquo;. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash; one of the most effective cancer drugs in medical history. 
 Learn more atSTARTresearch.com.  
 Ready to be part of a team changing the future of cancer treatment? 
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online. 
 We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Mon, 30 Mar 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Clinical Research Coordinator - San Antonio, TX]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27774481&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>2f7d488f-5f75-4201-975f-0d54ae9418ed</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largestearly phasesite network, fully dedicated tooncologyclinical research.Throughout ourhistory, START has provided hope to cancer patients inglobalcommunity practices by offering"Hope Through Access&rdquo;tocutting edgetrials throughout the UnitedStatesand Europe. 
We are hiring a Clinical Research Coordinator to work under the guidance of senior research staff to support the daily activities of early phase oncology clinical trials. The CRC ensures the accurate and timely conduct of clinical research, adhering to protocols, regulatory requirements, and patient safety standards. 
Location: 4383 Medical Dr, San Antonio, TX 78229
Work Hours: Monday-Friday 8am-5pm 
Essential Responsibilities

Communicate on a regular basis with Study Sponsor&rsquo;s, CRO&rsquo;s, staff, etc. regarding questions, concerns, as well as status of the protocol.  
Monitor the overall day-to-day conduct of assigned studies in accordance with the specified protocol requirements, Standard Operating Procedures, and Good Clinical Practice to ensure integrity regarding all aspects of the study.  
Create/review forms created or revised for assigned trials to assure protocol compliance.  
Maintain files using standardized study document labeling and filing procedures.  
Implement initial protocol and amendments, training staff who will be involved in patient treatment and management.  
Maintain an up-to-date contact list.  
Assist with patient screening and determination of eligibility.  
Facilitate the informed consent process ensuring that consent is appropriately completed.  
Prepare and manage source documents according to standard operating procedures.  
Recognize deviations to the protocol and will work with leadership and staff to address corrective actions to prevent deviations.  
Assist data coordinator team with case report form completion and query resolution.  
Work with the Principal Investigator to complete and submit Serious Adverse Event reports.  
Perform protocol specific closeout related activities in conjunction with the data coordinator.  
Provide documentation for all deviations whether related to the protocol or a SOP.  
Ensure that all team members involved understand and adhere to assigned protocols.  

Education & Experience

High School Diploma or GED. 
2 years of clinical research experience. 
Basic understanding of oncology clinical trials, particularly Phase 1 studies. 
Strong attention to detail and accuracy in data collection and documentation. 
Ability to manage multiple tasks and meet deadlines in a fast-paced environment. 
Excellent organizational and time-management skills. 
Strong communication skills, both written and verbal. 
Ability to interact professionally with patients, study staff, and external stakeholders. 
Working knowledge of GCP and regulatory requirements. 
Proficient in Microsoft Office Suite and clinical trial management software. 

Preferred Education and Experience: 

Experience working in an oncology setting. 

Physical and Travel Requirements:

Approximately 80% of time is spent sitting. 
Very fast-paced and ever-changing healthcare environment. 
Demanding deadlines and time frames. 
Constant demand for updating knowledge. 
Works closely with physicians and ancillary personnel in caring for and treating oncology/hematology patients. 

Best-in-Class Benefits and Perks
We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package&mdash;based on experience&mdash;along with comprehensive benefits designed to support you both personally and professionally: 
Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.




401(k) retirement savings plan with employer match 






Eligibility for an annual performance bonus, based on role and company results 






Generous paid time off and paid holidays 






Comprehensive medical, dental, and vision coverageand optional insuranceoptions 






Company paid life and disability insurance for added financial protection 






Employee Assistance Program (EAP) providing confidential, no cost support for you and your family from day one 








Flexible FSA and HSA plans to support your financial wellness 






Commitment to a supportive environment that values balance, wellbeing, and flexibility 






We&rsquo;recommitted to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START,you&rsquo;lljoin a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation. 




 
More about The START Center for Cancer Research
START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. STARTrepresentsthe world&rsquo;s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of &ldquo;Hope Through Access&rdquo;.As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash;one ofthe most effective cancerdrugsin medical history. Learn more atSTARTresearch.com. 

Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Yourexpertiseand dedication can help us bring hope and healing to patients worldwide.Pleasesubmityour application online. 

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Mon, 30 Mar 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[CRC Specialist (Remote) - East Brunswick, NJ]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27774477&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>df66c99a-40f2-4e3a-ac03-1fb2cf172f4c</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. To date, over 45 therapies conducted at START locations have obtained FDA/EMA approval. 
The START Center for Cancer Research is seeking a CRC Specialist to be responsible for leading the operational startup of new START USA sites by providing hands-on coordination and training in Phase I oncology trials. This role will temporarily fill the CRC role at launch sites, guide and mentor new CRC hires, and ensure the seamless execution of study start-up activities and early operations. In addition, this role will support existing START sites by covering CRC responsibilities during vacancies, ensuring no disruption in patient care or study conduct.  
This is a remote role with an annual base salary for this role is $80,000 - $100,000. However, base pay may vary depending on multiple individualized factors including market location, job-related knowledge, skills, and experience. 
Essential Responsibilities

Act as the interim CRC at new START sites during launch phase, managing study start-up, patient enrollment, and clinical coordination duties. 
Train and mentor the first on-site CRC at each new location, ensuring comprehensive onboarding to START SOPs, GCP compliance, and study-specific procedures. 
Serve as a trusted expert and role model for new and tenured CRCs across START USA. 
Travel to START sites as needed (approximately 50%) to support launch operations or in-person support for struggling sites. 
Support existing sites by covering CRC responsibilities during periods of leave, turnover, or unexpected staffing gaps. 
Collaborate with Study Operations leadership, Quality Assurance, and HR on continuous improvement of training programs and SOP implementation. 
Ensure protocol compliance, timely documentation, and coordination of patient-related activities for assigned studies, whether in-person or remote. 
Communicate effectively with site staff, investigators, sponsors, CROs, and patients to maintain study continuity and data integrity. 
Identify process inefficiencies or gaps and contribute to site-level or organizational CAPAs and workflow redesign initiatives. 
Participate in study start-up meetings, monitor protocol amendments, and ensure staff are trained on changes. 
Support implementation of best practices in patient consenting, AE/SAE documentation, and data collection across sites. 
Maintain expert-level understanding of current and evolving GCP, FDA, and institutional regulatory requirements. 

Required Education and Experience: 

High School Diploma or GED. 
5+ years of clinical research experience, with deep expertise in Phase I oncology trials. 
Proven record of successfully coordinating multiple complex protocols and mentoring other research staff. 
Exceptional communication, leadership, and training abilities. 
Demonstrated success in implementing quality improvement initiatives or standardization efforts. 
Strong command of clinical trial documentation, patient-facing procedures, and regulatory frameworks. 
Ability to travel up to 50% to various START USA locations as needed. 
Experience using clinical trial management systems (CTMS), EMRs, and sponsor IRT platforms. 

Preferred Education and Experience: 

Bachelor&rsquo;s degree. 
Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP). 
More than 5 years of experience in a lead CRC or trainer role within an oncology research setting. 
Formal training in adult learning principles or prior experience developing training materials. 

Physical & Travel Requirements: 

50% travel expected across U.S. sites for onsite coverage or training. 
When not traveling, work will be conducted remotely or at a START facility. 
Fast-paced, high-pressure environment with shifting priorities. 
Must be comfortable adapting to different site cultures and workflows. 

Best-in-Class Benefits and Perks
We value our employees&rsquo; time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:

Comprehensive health coverage: Medical, dental, and vision insurance provided
Robust retirement planning: 401(k) plan available with employer matching
Financial security: Life and disability insurance for added protection
Flexible financial options: Health savings and flexible spending accounts offered
Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided
Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.

More about The START Center for Cancer Research
Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including for 43 therapies that were approved by the FDA. START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. Learn more at STARTresearch.com.
Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.
We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Mon, 30 Mar 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[CTMS Entry Coordinator - Grand Rapids, MI]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27774495&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>664d7344-8d84-43f4-8624-b9e443b0e97e</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering "Hope Through Access&rdquo; to cutting edge trials throughout the United States and Europe.  
 We are seeking a CTMS Entry Coordinator.  This role will assist the Clinical Research Coordinators in all tasks to support their roles. It will require an understanding of research terminology and basic protocol interpretation.
Work Schedule: Monday-Friday, 8am-5pm
Location: 5800 Foremost Dr SE, Grand Rapids, MI 49546
Essential Responsibilities

Collect, de-identify, enter/transcribe, and transmit/submit clinical data in paper and/or electronic case reports forms (CRFs), including correction and query resolution for assigned investigational drug studies. This includes but is not limited to images, lab results, and ECGs. 
Collaborate with Clinical Research Coordinator to ensure data timepoints are accurate and provide query resolution.
Contact patients in follow-up as needed per protocol.
Review and utilize protocols as guides for study activities for assigned studies.
Assist with the setup and formatting of study-specific Eligibility, Study Schedules, and Flow Sheets documents per protocol.
Assist with CTMS upkeep, including but not limited to tracking patient visits, IRB re-consents, Serious Adverse Events (SAEs) and Deviations.
Ensure that data transmissions remain current for assigned studies.
Provide support and information to onsite and remote monitors as necessary.
Comply with all applicable regulations, guidelines, and procedures pertaining to data loading, EDC systems, and clinical research.
Share responsibility with Data Coordinators to identify lab facilities and normal lab values used for assigned studies so that lab certifications can be requested for the study file.
Attend meetings regarding assigned studies as needed, including site initiation visits, Roster meetings and Forms Committee.
Communicate as needed with accounts receivable staff regarding transmitted data.

 Required Education and Experience:

High School diploma or equivalent.
One year of research administrative experience within a healthcare, pharmaceutical, or research organization.
Knowledge and training in general office administration skills, including computer applications, filing systems, etc. 
Familiarity with medical terminology.
Strong organizational skills and a sense of timeliness in completing projects.
Must be detail-oriented and able to understand instructions and work independently. 

 Best-in-Class Benefits and Perks 
We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package&mdash;based on experience&mdash;along with comprehensive benefits designed to support you both personally and professionally:   

401(k) retirement savings plan with employer match 
Eligibility for an annual performance bonus, based on role and company results 
Generous paid time off and paid holidays 
Comprehensive medical, dental, and vision coverage and optional insurance options 
Companypaid life and disability insurance for added financial protection 
Employee Assistance Program (EAP) providing confidential, nocost support for you and your family from day one 
Flexible FSA and HSA plans to support your financial wellness 
Commitment to a supportive environment that values balance, wellbeing, and flexibility 
We&rsquo;re committed to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START, you&rsquo;ll join a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation. 

 More About START 
START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. START represents the world&rsquo;s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of &ldquo;Hope Through Access&rdquo;. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash; one of the most effective cancer drugs in medical history. 
 Learn more atSTARTresearch.com.  
 Ready to be part of a team changing the future of cancer treatment? 
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online. 
 We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Mon, 30 Mar 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Clinical Trial Finance Analyst (Remote) - San Antonio, TX]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27774547&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>48f76021-c81d-4e3f-af65-7e936f9053b5</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largestearly phasesite network, fully dedicated tooncologyclinical research.Throughout ourhistory, START has provided hope to cancer patients inglobalcommunity practices by offering"Hope Through Access&rdquo;tocutting edgetrials throughout the UnitedStatesand Europe.

The Clinical Trial Finance Analyst manages financial oversight for a portfolio of clinical research studies of varying complexity including multi-site and global trials. This role supports the financial oversight of clinical research studies by ensuring accurate billing, account reconciliations, patient visit validation, and vendor expense processing. This role collaborates with crossfunctional teams to maintain data accuracy, support monthend close activities, and drive continuous improvement across clinical finance processes.
This is a remote role. The annual base salary for this role is $65,000 - $75,000. However, base pay may vary depending on multiple individualized factors including market location, job-related knowledge, skills, and experience.  In addition, employees in this role may be eligible for an annual bonus of up to 10% of base earnings.

Essential Responsibilities:
&middot; Prepare, review, and approve (within delegated authority) monthly clinical trial invoices for domestic and international study sites.
&middot; Review and approve within delegated authority vendor invoices and studyrelated expenses for accuracy, contractual compliance, and documentation; ensure timely processing and billing alignment.
&middot; Maintain detail study-level reconciliations to ensure all patient visits, procedures, and expenses are accurately priced and billed.
&middot; Partner with domestic or international Accounts Receivable teams to ensure sponsor payments are applied accurately and timely.
&middot; Collaborate with study budget, contracting, and research teams to research, analyze, and resolve billing discrepancies.
&middot; Perform financial close-out activities, including final reconciliations and sponsor invoicing. 
&middot; Utilize NetSuite and CTMS platforms to manage financial workflows and maintain data integrity.
&middot; Conduct financial analysis of profitability, trends, and performance drivers; provide insights and recommendations.
&middot; Support month-end close activities, including accruals and variance analysis.
&middot; Other duties may be assigned at any time. 
 
Required Education & Experience:
&middot; Bachelor&rsquo;s degree in accounting, Finance, or a related field.
&middot; Minimum of 3+ years of experience in financial analysis or clinical research finance experience.
&middot; Experience with ERP systems (e.g., NetSuite) and CTMS platforms(e.g., OnCore by Advarra). 
&middot; Advanced Microsoft Excel skills (pivot tables, VLOOKUP/XLOOKUP).
&middot; Ability to reconcile and analyze large datasets.
&middot; Understanding of clinical research billing compliance, including protocols, budgets, contracts, and regulatory obligations.
&middot; Ability to identify and escalate billingrelated compliance risks.
&middot; Highly organized and detail-oriented in a fast-paced environment.
 
Preferred Education and Experience:
&middot; Experience with CRO/Sponsor-Facing roles.
&middot; Experience with clinical research finance or research organizations.
&middot; Multi-site/global study exposure.
&middot; Revenue recognition or accrual accounting experience.
 
Physical & Travel Requirements:
&middot; Sitting: Must be able to sit for extended periods of time. 
&middot; Prolonged use of computer, keyboard, and mouse. 
 
Best-in-Class Benefits and Perks
We value our employees&rsquo; time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:




401(k) retirement savings plan with employer match 






Eligibility for an annual performance bonus, based on role and company results 






Generous paid time off and paid holidays 






Comprehensive medical, dental, and vision coverageand optional insuranceoptions 






Company paid life and disability insurance for added financial protection 






Employee Assistance Program (EAP) providing confidential, no cost support for you and your family from day one 








Flexible FSA and HSA plans to support your financial wellness 






Commitment to a supportive environment that values balance, wellbeing, and flexibility 






We&rsquo;recommitted to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START,you&rsquo;lljoin a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation. 




 
More about The START Center for Cancer Research
START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. STARTrepresentsthe world&rsquo;s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of &ldquo;Hope Through Access&rdquo;.As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash;one ofthe most effective cancerdrugsin medical history. 

Learn more atSTARTresearch.com. 


Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Mon, 30 Mar 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Oncology Nurse Navigator - Grand Rapids, MI]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27774491&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>c2f50804-0d03-4d6b-83af-453446447d63</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. To date, over 45 therapies conducted at START locations have obtained FDA/EMA approval. 
The START Center for Cancer Research is seeking a Nurse Navigator who will serve as the primary liaison between patients, referring physicians, and START staff. This role ensures timely, coordinated, and personalized care while addressing barriers to trial participation, promoting program awareness, and enhancing patient outcomes.
Essential Responsibilities

Educate referring physicians and their staff about the START Phase 1 program and clinical trials. 
Perform referral intake for new patients, ensuring coordinated, high-quality care and service. 
Identify opportunities to leverage technology for improved patient matching and care coordination. 
Support patients by scheduling Phase 1 appointments, addressing barriers to care, and linking them with community resources. 
Present new and ongoing trials referring physicians and staff using virtual and in-person platforms. 
Coordinate case conferences and attend tumor boards to support multidisciplinary cancer care. 
Maintain accurate and timely documentation for Phase 1 patient tracking and study monitoring. 
Attend administrative meetings, protocol reviews, and site visits as required. 
Demonstrate effective communication and maintain confidentiality of patient information. 
Practice integrity and accountability, incorporating feedback into clinical presentations. 
Support growth goals of the clinical research program with respect to new patient referrals and accruals. 

Required Education and Experience: 

Associate&rsquo;s degree. 
Active Registered Nurse (RN) license in the practicing state. 
Minimum of 1 year of oncology experience.

Preferred Education and Experience: 

Oncology Certified Nurse (OCN) certification. 
Clinical trials experience. 

Physical & Travel Requirements: 

Travel may be required to referral offices or for presentations. 
Ability to sit or stand for prolonged periods. 

Best-in-Class Benefits and Perks
We value our employees&rsquo; time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:

Comprehensive health coverage: Medical, dental, and vision insurance provided
Robust retirement planning: 401(k) plan available with employer matching
Financial security: Life and disability insurance for added protection
Flexible financial options: Health savings and flexible spending accounts offered
Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided
Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.

More about The START Center for Cancer Research
Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including for 43 therapies that were approved by the FDA. START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. Learn more at STARTresearch.com.
Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.
We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Mon, 30 Mar 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Scheduler - West Valley City, UT]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27774441&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>1a80706c-b5c3-4127-8226-491b9d515f7b</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. To date, over 45 therapies conducted at START locations have obtained FDA/EMA approval. 
The START Center for Cancer Research is seeking a Scheduler, for our West Valley City, Utah location at 2965 W 3500 S, West Valley City, UT 84119. This role will facilitate excellent patient care by supporting and collaborating with the clinic team. This is a fully on-site role. The hours are 7:00am-3:30pm, Monday through Friday. Some flexibility may be needed based on needs of the clinic.
Essential Responsibilities

Manage scheduling for study-specific appointments, radiology procedures, and travel arrangements.
Ensure prior authorizations are completed.
Handle administrative tasks, including follow-ups, referrals, no-shows, and rescheduling.
Maintain accurate electronic medical records and manage documentation.
Communicate with patients and care team members to ensure coordinated care.
Support quality improvement initiatives for efficient, cost-effective care.
Participate in ongoing education and training to maintain skills and competency.

Required Education and Experience: 

High School Diploma or equivalent. 
One year experience in an outpatient physician practice or healthcare setting. 
Effective communication skills and collaborative attitude. 
Strong attention to detail. 
Knowledge of medical terminology as it relates to scheduling study specific procedures such as CT/MRI/PET scans, biopsies, eye exams, etc.

Preferred Education and Experience: 

Oncology and/or research experience. 

Best-in-Class Benefits and Perks
We value our employees&rsquo; time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:

Comprehensive health coverage: Medical, dental, and vision insurance provided
Robust retirement planning: 401(k) plan available with employer matching
Financial security: Life and disability insurance for added protection
Flexible financial options: Health savings and flexible spending accounts offered
Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided
Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.

More about The START Center for Cancer Research
Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including for 43 therapies that were approved by the FDA. START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. Learn more at STARTresearch.com.
Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.
We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Fri, 27 Mar 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Clinical Research Coordinator - Lake Success,, NY]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27774159&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>1eb92abf-a02c-4c94-b0da-d136b85d6a0a</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largestearly phasesite network, fully dedicated tooncologyclinical research.Throughout ourhistory, START has provided hope to cancer patients inglobalcommunity practices by offering"Hope Through Access&rdquo;tocutting edgetrials throughout the UnitedStatesand Europe. 
We are hiring a Clinical Research Coordinator to work under the guidance of senior research staff to support the daily activities of early phase oncology clinical trials. The CRC ensures the accurate and timely conduct of clinical research, adhering to protocols, regulatory requirements, and patient safety standards. 
This position is offered at a pay range of $30.00 to $44.00 per hour, based on experience, qualifications, and internal equity. In addition, employees in this role may be eligible for an annual bonus of up to 10% of base earnings.
Work Schedule: 8:00 am-5:00 pm EST, Monday-Friday 
Location: 405 Lakeville Road, Entrance A, Lake Success, NY 11042
Essential Responsibilities

Communicate on a regular basis with Study Sponsor&rsquo;s, CRO&rsquo;s, staff, etc. regarding questions, concerns, as well as status of the protocol.  
Monitor the overall day-to-day conduct of assigned studies in accordance with the specified protocol requirements, Standard Operating Procedures, and Good Clinical Practice to ensure integrity regarding all aspects of the study.  
Create/review forms created or revised for assigned trials to assure protocol compliance.  
Maintain files using standardized study document labeling and filing procedures.  
Implement initial protocol and amendments, training staff who will be involved in patient treatment and management.  
Maintain an up-to-date contact list.  
Assist with patient screening and determination of eligibility.  
Facilitate the informed consent process ensuring that consent is appropriately completed.  
Prepare and manage source documents according to standard operating procedures.  
Recognize deviations to the protocol and will work with leadership and staff to address corrective actions to prevent deviations.  
Assist data coordinator team with case report form completion and query resolution.  
Work with the Principal Investigator to complete and submit Serious Adverse Event reports.  
Perform protocol specific closeout related activities in conjunction with the data coordinator.  
Provide documentation for all deviations whether related to the protocol or a SOP.  
Ensure that all team members involved understand and adhere to assigned protocols.  
Other duties may be assigned at any time. 

Education & Experience

High School Diploma or GED. 
2 years of clinical research experience. 
Basic understanding of oncology clinical trials, particularly Phase 1 studies. 
Strong attention to detail and accuracy in data collection and documentation. 
Ability to manage multiple tasks and meet deadlines in a fast-paced environment. 
Excellent organizational and time-management skills. 
Strong communication skills, both written and verbal. 
Ability to interact professionally with patients, study staff, and external stakeholders. 
Working knowledge of GCP and regulatory requirements. 
Proficient in Microsoft Office Suite and clinical trial management software. 

Preferred Education and Experience: 

Experience working in an oncology setting. 

Physical and Travel Requirements:

Approximately 80% of time is spent sitting. 
Very fast-paced and ever-changing healthcare environment. 
Demanding deadlines and time frames. 
Constant demand for updating knowledge. 
Works closely with physicians and ancillary personnel in caring for and treating oncology/hematology patients. 

Best-in-Class Benefits and Perks
We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package&mdash;based on experience&mdash;along with comprehensive benefits designed to support you both personally and professionally: 
Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.




401(k) retirement savings plan with employer match 






Eligibility for an annual performance bonus, based on role and company results 






Generous paid time off and paid holidays 






Comprehensive medical, dental, and vision coverageand optional insuranceoptions 






Company paid life and disability insurance for added financial protection 






Employee Assistance Program (EAP) providing confidential, no cost support for you and your family from day one 








Flexible FSA and HSA plans to support your financial wellness 






Commitment to a supportive environment that values balance, wellbeing, and flexibility 






We&rsquo;recommitted to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START,you&rsquo;lljoin a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation. 




 
More about The START Center for Cancer Research
START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. STARTrepresentsthe world&rsquo;s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of &ldquo;Hope Through Access&rdquo;.As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash;one ofthe most effective cancerdrugsin medical history. Learn more atSTARTresearch.com. 

Ready to be part of a team changing the future of cancer treatment? 
Join us in our mission to conquer cancer, one clinical trial at a time. Yourexpertiseand dedication can help us bring hope and healing to patients worldwide.Pleasesubmityour application online. 

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Tue, 24 Mar 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Manager, Regulatory Operations (Remote) - San Antonio, TX]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27774130&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>d199122b-cfd0-4705-8284-2ba12d59948c</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. To date, over 45 therapies conducted at START locations have obtained FDA/EMA approval. 
The START Center for Cancer Research is seeking a Manager, Regulatory Operations who will lead and develop a team (that includes Specialists), and Assistants to ensure timely, accurate, and compliant regulatory submissions and maintenance of inspection-ready Investigator Site Files (ISFs). The Manager, Regulatory Operations is accountable for team performance, process standardization, metrics, training and onboarding, and continuous improvement of systems and workflows supporting IRB, IBC, and FDA interactions, in alignment with applicable regulations and guidelines (e.g., GCP, FDA BIMO, 21 CFR Part 11). 
This is a remote role. The annual base salary for this role is $105,000 - $135,000. However, base pay may vary depending on multiple individualized factors including market location, job-related knowledge, skills, and experience. 
Essential Responsibilities

Provide direct people leadership for assigned team. 
Partner with the Regulatory Operations Leadership and Quality Assurance to set departmental goals and ensure timely execution of regulatory deliverables that support study startup, conduct, maintenance and close out.  
Oversee day to day regulatory operations to ensure submissions are accurate, complete and on time; balance workloads and assign / re-distribute studies based on capacity and complexity. 
Establish, maintain, and continuously improve SOPs, work instructions, templates, and training materials to drive standardization, quality, and scalability across sites. 
Maintain relationships with Institutional Review Board(s) (IRB) used and Sponsors/CROs. 
Supervise day-to-day activities of the Regulatory Operations staff to ensure that submissions are accurate, and deadlines are met. 
Monitor key metrics (e.g., turnaround times, aging, quality findings) and drive corrective actions and process improvements in partnership with Quality Assurance and cross-functional stakeholders. 
Serve as an escalation point for complex regulatory issues and facilitate timely resolution with IRBs, IBCs, FDA, Sponsors/CROs, and other departments.  
Attend SOP Committee Meetings quarterly, provide regulatory and data input, and revise any SOPs as needed per the meetings. 
Collaborate with other START departments, including Site Clinical departments and Shared Services departments, and Regional Director to provide support and leadership to effectively meet deadlines, prepare for audits, manage various electronic systems and START templates in use at START (i.e., FileMaker, CITI portal, study portals, e-signature platforms, etc.), and special projects as needed. 
Prepare and submit new studies, including drafting the informed consent (IC), to the IRB (local and hospital) as assigned. Serve as the main point of contact with the Sponsor/CRO in negotiating the IC for IRB submission. Serve as the main point of contact with the IRB(s) for the studies. Enter submission dates in FileMaker database, note pending information, and generate status reports as required. Respond to inquiries and follow up on pending items.  
Prepare and submit study documents to the IRB (local and hospital) for assigned studies. This includes, but is not limited to, revised protocols, revised investigator&rsquo;s brochures, protocol clarification letters/memos, revised ICs, new ICs, continuing review reports, closure reports, serious adverse events, IND safety reports, unanticipated problems, protocol deviations, and waivers. Serve as the main point of contact with the IRB(s) for the studies. Enter submission dates in FileMaker database, note pending information, and generate status reports as required. Respond to inquiries and follow up on pending items. 
Prepare and submit study documents to the Institutional Biosafety Committee (IBC) as assigned.  Serve as the main point of contact with the IBC for the studies.  Enter submission dates in FileMaker database, note pending information, and generate status reports as required.  Respond to inquiries and follow up, as required, on pending items. 
Prepare and submit Expanded Access Studies to the US Food and Drug Administration (FDA) as assigned. Serve as the main point of contact with the FDA and IRB for the studies. Enter submission dates in FileMaker database, note pending information, and generate status reports as required. Respond to inquiries and follow up, as required, on pending items. 
Maintain the ISF (paper and/or electronic) for assigned studies.  This includes, but is not limited to, IRB submissions, IRB approvals, study documents, and study correspondence. 
Prepare and manage Close-Out Visits for assigned studies. 

Education & Experience

Bachelor&rsquo;s degree or equivalent experience in lieu of degree.   
5+ years of progressive experience in a regulatory research setting, including oversight of new study submissions and ongoing maintenance and management experience. 
Proficiency with Microsoft Office and Regulatory Data Tracking / Document Management Systems (e.g., Jira, Veeva, Advarra E-Reg). 
Excellent leadership, organizational, and communication skills with a high level of attention to detail. 
Advanced working knowledge of IRB, FDA, and IBC requirements with experience supporting audit / inspection readiness.  

Physical and Travel Requirements:

Travel required up to 10% of the time 
Sitting for extended periods of time. 
Typing and computer use for extended periods of time. 

Best-in-Class Benefits and Perks
We value our employees&rsquo; time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:

Comprehensive health coverage: Medical, dental, and vision insurance provided
Robust retirement planning: 401(k) plan available with employer matching
Financial security: Life and disability insurance for added protection
Flexible financial options: Health savings and flexible spending accounts offered
Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided
Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.

More about The START Center for Cancer Research
Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including for 43 therapies that were approved by the FDA. START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. Learn more at STARTresearch.com.
Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.
We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Tue, 24 Mar 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Clinical Data Entry Coordinator - Lake Success,, NY]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27774153&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>ff4bcd0d-4589-49b8-97cc-2f6a26b8ec85</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largestearly phasesite network, fully dedicated tooncologyclinical research.Throughout ourhistory, START has provided hope to cancer patients inglobalcommunity practices by offering"Hope Through Access&rdquo;tocutting edgetrials throughout the UnitedStatesand Europe.

We are hiring a motivated Clinical Data Entry Coordinator who will collect, enter/transcribe, and transmit/submit clinical data for assigned investigational drug studies. 
This position is offered at a pay range of $24.00 to $27.00 per hour, based on experience, qualifications, and internal equity. In addition, employees in this role may be eligible for an annual bonus of up to 10% of base earnings.
Work Schedule: 8:00 am-5:00 pm EST, Monday-Friday 
Location: 405 Lakeville Road, Entrance A, Lake Success, NY 11042
Essential Responsibilities

Collect, enter/transcribe, and transmit/submit clinical data in paper and/or electronic case report forms (CRFs), including correction and query resolution for assigned investigational drug studies.
Receive and request patient records/data from the study team as required to complete CRFs for assigned studies. 
Review patient data for completeness and accuracy for assigned studies.
Coordinate and schedule monitor visits for assigned studies.  This includes exit meetings with monitors to review data or queries.
Identify lab facilities used for assigned studies and communicate to the Regulatory Affairs staff so that lab certifications can be requested for the study file.
Review and utilize protocols as guides for study activities for assigned studies.
Assure that data entry remains current for all assigned studies.
Attend meetings as required for assigned studies.  This includes, but is not limited to, site initiation meetings, monitor exit meetings, close-out visit meetings, and audit preparation meetings.
Be available and on-site, if required, during audits for assigned studies.
Communicate as needed with accounts receivable staff regarding submitted data. 

Education & Experience

Bachelor&rsquo;s degree or equivalent experience in lieu of degree. 
Knowledge and training in general office administration skills, including computer applications, filing systems, etc.

Preferred Education and Experience

Ability to accurately perform data review and CRF completion in its entirety with minimal direction. 
Familiarity with medical terminology.
Additional demonstration of clinical research knowledge as evidenced by the use of either CCRP or CCRC credentials is highly desirable. 

Best-in-Class Benefits and Perks
We value our employees&rsquo; time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:

Comprehensive health coverage: Medical, dental, and vision insurance provided
Robust retirement planning: 401(k) plan available with employer matching
Financial security: Life and disability insurance for added protection
Flexible financial options: Health savings and flexible spending accounts offered
Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided
Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.


More about The START Center for Cancer Research
Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including for 43 therapies that were approved by the FDA. START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. Learn more at STARTresearch.com.

Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Tue, 24 Mar 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Oncology Nurse Navigator - East Brunswick, NJ]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27774042&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>ac449020-a673-4bef-b4c4-333b9bc0fe1a</guid>
      <description><![CDATA[&bull;      The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering "Hope Through Access&rdquo; to cutting edge trials throughout the United States and Europe.  
 The Oncology Nurse Navigator is a critical member of the Phase 1 clinical trial program team, serving as the primary liaison between patients, referring physicians, and START staff. This role ensures timely, coordinated, and personalized care while addressing barriers to trial participation, promoting program awareness, and enhancing patient outcomes.
Work Schedule: Monday-Friday, 8am-5pm
Location: East Brunswick, NJ
Pay Range: $104K-$145,600K
 Essential Responsibilities:

 Educate referring physicians and their staff about the START Phase 1 program and clinical trials.
Perform referral intake for new patients, ensuring coordinated, high-quality care and service.
Identify opportunities to leverage technology for improved patient matching and care coordination.
Support patients by scheduling Phase 1 appointments, addressing barriers to care, and linking them with community resources.
Present new and ongoing trials referring physicians and staff using virtual and in-person platforms.
Coordinate case conferences and attend tumor boards to support multidisciplinary cancer care.
Maintain accurate and timely documentation for Phase 1 patient tracking and study monitoring.
Attend administrative meetings, protocol reviews, and site visits as required.
Demonstrate effective communication and maintain confidentiality of patient information.
Practice integrity and accountability, incorporating feedback into clinical presentations.
Support growth goals of the clinical research program with respect to new patient referrals and accruals..

Education & Experience:

Associate&rsquo;s degree.
Active Registered Nurse (RN) license in the practicing state.
Minimum of 1 year of oncology experience.

 Preferred Education and Experience:   

Oncology Certified Nurse (OCN) certification.
Clinical trials experience.

Physical & Travel Requirements 

Travel may be required to referral offices or for presentations.

 Best-in-Class Benefits and Perks 
We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package&mdash;based on experience&mdash;along with comprehensive benefits designed to support you both personally and professionally:  

401(k) retirement savings plan with employer match 
Eligibility for an annual performance bonus, based on role and company results 
Generous paid time off and paid holidays 
Comprehensive medical, dental, and vision coverage and optional insurance options 
Companypaid life and disability insurance for added financial protection 
Employee Assistance Program (EAP) providing confidential, nocost support for you and your family from day one 
Flexible FSA and HSA plans to support your financial wellness 
Commitment to a supportive environment that values balance, wellbeing, and flexibility 
We&rsquo;re committed to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START, you&rsquo;ll join a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation. 

 More About START 
START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. START represents the world&rsquo;s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of &ldquo;Hope Through Access&rdquo;. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash; one of the most effective cancer drugs in medical history. 
 Learn more atSTARTresearch.com.  
 Ready to be part of a team changing the future of cancer treatment? 
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online. 
 We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Mon, 23 Mar 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Scheduler - Fort Worth, TX]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27774050&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>87a788d0-6f32-4f17-a2af-027b4dde92a4</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering "Hope Through Access&rdquo; to cutting edge trials throughout the United States and Europe.  
We are seeking a Scheduler, who will facilitate excellent patient care by supporting and collaborating with the clinic team. 
Work Schedule:  8:00am-5:00pm M-F
Location:    Dallas Forth Worth, TX
 Essential Responsibilities:

Manage scheduling protocol specific Study Schedules including, but not limited to, scheduling appointments, radiology procedures and booking hotel stays.
Ensure prior authorizations are completed.
Perform administrative responsibilities, including, but not limited to, scheduling routine follow-up and treatment appointments, managing external referrals and consults, handling no-shows, answering phone calls, and rescheduling patients.
Perform the day-to-day delivery of quality services through consistent application of policies, procedures, protocols, and standards.
Communicate with patients and visitors in a caring and respectful manner. Collaborate with other care team members and anticipate their needs to ensure coordinated patient care.
Use and maintain patient electronic medical records, including filing, faxing, and copying.
Assist with ongoing quality improvements to provide efficient, cost-effective care.
Engage in continuous education and training to maintain skills, knowledge, and competency to complete functions of role.

 Education & Experience:

High School Diploma or equivalent.
One year experience in an outpatient physician practice or healthcare setting.
Effective communication skills and collaborative attitude.
Strong attention to detail.
Knowledge of medical terminology as it relates to scheduling study specific procedures such as CT/MRI/PET scans, biopsies, eye exams, etc

Preferred Education and Experience:

Oncology and/or research experience.

 Best-in-Class Benefits and Perks 
We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package&mdash;based on experience&mdash;along with comprehensive benefits designed to support you both personally and professionally:

 401(k) retirement savings plan with employer match 
Eligibility for an annual performance bonus, based on role and company results 
Generous paid time off and paid holidays 
Comprehensive medical, dental, and vision coverage and optional insurance options 
Company  paid life and disability insurance for added financial protection 
Employee Assistance Program (EAP) providing confidential, no cost support for you and your family from day one 
Flexible FSA and HSA plans to support your financial wellness 
Commitment to a supportive environment that values balance, wellbeing, and flexibility 
We&rsquo;re committed to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START, you&rsquo;ll join a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation. 

 More About START 
START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. START represents the world&rsquo;s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of &ldquo;Hope Through Access&rdquo;. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash; one of the most effective cancer drugs in medical history. 
 Learn more atSTARTresearch.com.  
 Ready to be part of a team changing the future of cancer treatment? 
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online. 
 We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Mon, 23 Mar 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Regulatory Operations Assistant - La Rioja, LO]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27774127&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>f1b977fd-8393-4ab0-91c3-5058dfb91604</guid>
      <description><![CDATA[START Center for Cancer Research (&ldquo;START&rdquo;) es la mayor red mundial de centros de fase I, dedicada por completo a la investigaci&oacute;n cl&iacute;nica oncol&oacute;gica. A lo largo de nuestra historia, START ha proporcionado esperanza a pacientes con c&aacute;ncer en consultas de comunidades globales, ofreci&eacute;ndoles acceso a ensayos de vanguardia en Estados Unidos y Europa. En la actualidad, con m&aacute;s de 1.300 estudios realizados y con centros de investigaci&oacute;n en Estados Unidos y en Espa&ntilde;a, Portugal e Irlanda, la misi&oacute;n de START es acelerar el desarrollo de nuevos medicamentos contra el c&aacute;ncer que mejoren la calidad de vida y la supervivencia de los pacientes con c&aacute;ncer y conduzcan a su eventual curaci&oacute;n. Hasta la fecha, m&aacute;s de 43 terapias realizadas en centros START han obtenido la aprobaci&oacute;n de la FDA/EMA.
Vacante disponible: Regulatory Operations Assistant 
Responsabilidades:


Mantener el Investigator Site File (ISF) en papel y/o formato electr&oacute;nico para los estudios asignados, incluyendo env&iacute;os y aprobaciones del Comit&eacute; &Eacute;tico, documentos del estudio y correspondencia.
Crear y actualizar los registros de Delegaci&oacute;n de Autoridad y otros sistemas relacionados, incluyendo su revisi&oacute;n y cierre al finalizar el estudio.
Obtener las firmas necesarias del Investigador en protocolos, enmiendas, manuales del investigador, logs u otros documentos del estudio y enviarlos al patrocinador/CRO correspondiente.
Recibir y archivar informes de seguridad (IND, SUSAR y otros reportes interinos) en el ISF.
Gestionar visitas de monitorizaci&oacute;n relacionadas con operaciones regulatorias: dar acceso al ISF, resolver dudas y registrar cambios de monitor en los sistemas.
Recibir, gestionar para firma (si aplica) y archivar cartas del monitor.
Archivar documentaci&oacute;n de formaci&oacute;n (protocolo, EDC, GCP).
Mantener y actualizar CVs, licencias del Investigador y del equipo aplicable.
Preparar ISF para archivo realizando un control de calidad final y registrando en los sistemas qu&eacute; documentos quedan incluidos.
Recopilar y archivar certificados IATA del personal del estudio.
Completar y obtener firmas del Investigador para formularios 1572 o equivalentes y Formularios de Revelaci&oacute;n Financiera.
Gestionar versiones revisadas de documentos del estudio (enmiendas, cartas del protocolo, manuales del investigador) para env&iacute;o al Comit&eacute; &Eacute;tico, actualizando los archivos regulatorios y los sistemas correspondientes (incluido CTMS).
Mantener certificaciones de laboratorio, rangos normales y CVs/licencias de Directores de Laboratorio.
Archivar documentos de calibraci&oacute;n del equipamiento utilizado.
Ayudar en la revisi&oacute;n del ISF para auditor&iacute;as e inspecciones.
Colaborar con el equipo para cumplir m&eacute;tricas del departamento.
Conceder acceso al eISF al nuevo personal.
Realizar otras tareas asignadas.

Requisitos:

Inter&eacute;s en el &aacute;mbito sanitario
Se valorar&aacute; experiencia previa en ensayos cl&iacute;nicos
Persona proactiva y con capacidad de organizaci&oacute;n.
Excelente responsabilidad y atenci&oacute;n al detalle
Habilidad para trabajar en equipo y mantener una buena comunicaci&oacute;n con los compa&ntilde;eros y supervisores.
Nivel de ingl&eacute;s intermedio 

Beneficios

Jornada de Lunes a Viernes
28 d&iacute;as laborables de vacaciones
Retribuci&oacute;n flexible
Posibilidad de realizar clases particulares de ingl&eacute;s totalmente gratuitas

&iquest;Est&aacute; preparado para formar parte de un equipo que cambiar&aacute; el futuro del tratamiento del c&aacute;ncer?
&Uacute;nase a nosotros en nuestra misi&oacute;n de vencer al c&aacute;ncer, ensayo cl&iacute;nico a ensayo. Su experiencia y dedicaci&oacute;n pueden ayudarnos a llevar esperanza y curaci&oacute;n a pacientes de todo el mundo. Env&iacute;a tu solicitud en l&iacute;nea.]]></description>
      <pubDate>Mon, 23 Mar 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Oncology Nurse Navigator - Fort Worth, TX]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27774049&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>54c94ad3-e10d-4d9d-afe0-8ccbd1b41752</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering "Hope Through Access&rdquo; to cutting edge trials throughout the United States and Europe.  
 The Oncology Nurse Navigator is a critical member of the Phase 1 clinical trial program team, serving as the primary liaison between patients, referring physicians, and START staff. This role ensures timely, coordinated, and personalized care while addressing barriers to trial participation, promoting program awareness, and enhancing patient outcomes.
Work Schedule: Monday-Friday, 8am-5pm
Location: Dallas Fort Worth, TX
 Essential Responsibilities:

 Educate referring physicians and their staff about the START Phase 1 program and clinical trials.
Perform referral intake for new patients, ensuring coordinated, high-quality care and service.
Identify opportunities to leverage technology for improved patient matching and care coordination.
Support patients by scheduling Phase 1 appointments, addressing barriers to care, and linking them with community resources.
Present new and ongoing trials referring physicians and staff using virtual and in-person platforms.
Coordinate case conferences and attend tumor boards to support multidisciplinary cancer care.
Maintain accurate and timely documentation for Phase 1 patient tracking and study monitoring.
Attend administrative meetings, protocol reviews, and site visits as required.
Demonstrate effective communication and maintain confidentiality of patient information.
Practice integrity and accountability, incorporating feedback into clinical presentations.
Support growth goals of the clinical research program with respect to new patient referrals and accruals.

Education & Experience:

Associate&rsquo;s degree.
Active Registered Nurse (RN) license in the practicing state.
Minimum of 1 year of oncology experience.

 Preferred Education and Experience:   

Oncology Certified Nurse (OCN) certification.
Clinical trials experience.

Physical & Travel Requirements  

Travel may be required to referral offices or for presentations.

 Best-in-Class Benefits and Perks 
We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package&mdash;based on experience&mdash;along with comprehensive benefits designed to support you both personally and professionally:  

401(k) retirement savings plan with employer match 
Eligibility for an annual performance bonus, based on role and company results 
Generous paid time off and paid holidays 
Comprehensive medical, dental, and vision coverage and optional insurance options 
Companypaid life and disability insurance for added financial protection 
Employee Assistance Program (EAP) providing confidential, nocost support for you and your family from day one 
Flexible FSA and HSA plans to support your financial wellness 
Commitment to a supportive environment that values balance, wellbeing, and flexibility 
We&rsquo;re committed to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START, you&rsquo;ll join a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation. 

 More About START 
START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. START represents the world&rsquo;s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of &ldquo;Hope Through Access&rdquo;. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash; one of the most effective cancer drugs in medical history. 
 Learn more atSTARTresearch.com.  
 Ready to be part of a team changing the future of cancer treatment? 
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online. 
 We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Mon, 23 Mar 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Patient Navigator - East Brunswick, NJ]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27774040&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>be673345-6dcc-49cd-9023-18d36b422dad</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering "Hope Through Access&rdquo; to cutting edge trials throughout the United States and Europe.  
 We are seeking a Patient Navigator.  The Patient Navigator facilitates patient referrals for the START Phase 1 program. This role involves managing referral documentation, monitoring referral metrics, and supporting outreach activities.The Patient Navigator ensures a smooth intake process and efficient communication with referring providers  
Work Schedule: Monday-Friday, 8am-5pm
Location: East Brunswick, NJ
Pay Range: $23/hr-$28/hr
 Essential Responsibilities

Perform referral intake and assist with patient and provider coordination.
Maintain referral documentation and monitor referral trends.
Screen patients using EMR systems and genomic platforms for eligibility.
Support the Nurse Navigator in program outreach and trial promotion.
Participate in program meetings and contribute to data tracking efforts.
Other duties as assigned.

 Education & Experience:

High School Diploma or GED.
Minimum of 2 years of experience in clinical or administrative settings.
1 year of oncology experience.

 Preferred Education and Experience:   

Associate&rsquo;s degree in healthcare or related field.
Clinical trial experience.
Strong organizational and communication skills..

 Best-in-Class Benefits and Perks 
We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package&mdash;based on experience&mdash;along with comprehensive benefits designed to support you both personally and professionally:  

401(k) retirement savings plan with employer match 
Eligibility for an annual performance bonus, based on role and company results 
Generous paid time off and paid holidays 
Comprehensive medical, dental, and vision coverage and optional insurance options 
Companypaid life and disability insurance for added financial protection 
Employee Assistance Program (EAP) providing confidential, nocost support for you and your family from day one 
Flexible FSA and HSA plans to support your financial wellness 
Commitment to a supportive environment that values balance, wellbeing, and flexibility 
We&rsquo;re committed to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START, you&rsquo;ll join a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation. 

 More About START 
START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. START represents the world&rsquo;s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of &ldquo;Hope Through Access&rdquo;. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash; one of the most effective cancer drugs in medical history. 
 Learn more atSTARTresearch.com.  
 Ready to be part of a team changing the future of cancer treatment? 
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online. 
 We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Mon, 23 Mar 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Infusion Nurse Manager - West Valley City, UT]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27774032&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>e6028807-1a25-4e6b-b8e4-9e5ac544e801</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering "Hope Through Access&rdquo; to cutting edge trials throughout the United States and Europe.  
 The Nurse Manager oversees the infusion nursing team providing care for Phase 1 oncology patients. This role is responsible for ensuring the delivery of high-quality, evidence-based nursing care, managing infusion operations, and coordinating with clinical research teams to ensure adherence to protocols. The Nurse Manager is also responsible for the professional development, training, and competency of the nursing staff, while fostering a collaborative and patient-centered care environment.
Work Schedule:  8:00am-5:00pm M-F
Location: West Valley, UT
Essential Responsibilities:
&middot;       Leadership and Supervision: Provide proactive leadership and supervision to the team of infusion nurses and supporting clinical roles including the scheduling team. Support team members in achieving both individual and department goals, ensuring efficient, high-quality patient care.
&middot;       Staff Development: Mentor and develop the infusion nursing team through ongoing training, education, and performance evaluations. Ensure that nurses have the necessary skills and knowledge to manage Phase 1 oncology patients safely and effectively.
&middot;       Clinical Oversight: Ensure that infusion treatments are delivered in accordance with established protocols, patient care plans, and safety standards. Provide clinical support and guidance to nurses, assisting with complex cases and ensuring the highest standard of care.
&middot;       Quality Assurance: Monitor and maintain adherence to internal standard operating procedures and ensure ongoing compliance with clinical research protocols, federal regulations, and organizational policies.
&middot;       Patient Care Coordination: Oversee the coordination of care for Phase 1 oncology patients, including facilitating communication between the infusion team, research coordinators, and other healthcare providers. Ensure timely scheduling of infusions and address any time-sensitive issues that arise.
&middot;       Process Improvement: Lead continuous quality improvement initiatives to optimize workflows, improve patient outcomes, and enhance operational efficiency within the infusion unit. Address areas for improvement proactively and ensure staff adherence to new processes.
&middot;       Protocol Feasibility and Support: Review Phase 1 oncology study protocols to assess their feasibility with respect to nursing operations. Collaborate with research coordinators and other clinical staff to ensure seamless integration of research protocols into clinical care.
&middot;       Collaboration: Foster effective communication and collaboration with other clinical and administrative departments, including regulatory, PK lab, pharmacy, clinical research, and finance teams, to ensure compliance and successful patient outcomes.
&middot;       Documentation and Compliance: Ensure that all infusion procedures, patient interactions, and research-related activities are documented accurately in EHR and other relevant systems. Maintain compliance with clinical research regulations (GCP, FDA, HIPAA, etc.).
&middot;       Performance Metrics: Track and evaluate key performance metrics related to infusion operations, patient care, staff performance, and research study adherence. Provide regular reports and recommendations for improvement to senior leadership.
&middot;       Resource Management: Ensure appropriate staffing levels and resources are available to meet patient care needs. Work with senior management to address 
&middot;       staffing or equipment shortages.
 
 
 
 
 Education & Experience
&middot;       Bachelor&rsquo;s degree in Nursing (BSN) or higher.
&middot;       Current RN license in good standing with the state.
&middot;       ONS/ONCC chemotherapy and immunotherapy certification (or willingness to obtain).
&middot;       Extensive experience in oncology nursing, particularly with Phase 1 clinical trials or infusion services.
&middot;       Knowledge of GCP, federal research regulations, and clinical research protocols.
&middot;       Proficient in Microsoft Office applications and clinical documentation systems.
 
Preferred Experience
&middot;       Advanced degree in nursing, leadership, or a related field.
&middot;       Oncology Certified Nurse (OCN) certification.
&middot;       Previous experience managing a team of oncology or infusion nurses in a clinical research setting.
 
 
Best-in-Class Benefits and Perks 
We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package&mdash;based on experience&mdash;along with comprehensive benefits designed to support you both personally and professionally:  

401(k) retirement savings plan with employer match 
Eligibility for an annual performance bonus, based on role and company results 
Generous paid time off and paid holidays 
Comprehensive medical, dental, and vision coverage and optional insurance options 
Companypaid life and disability insurance for added financial protection 
Employee Assistance Program (EAP) providing confidential, nocost support for you and your family from day one 
Flexible FSA and HSA plans to support your financial wellness 
Commitment to a supportive environment that values balance, wellbeing, and flexibility 
We&rsquo;re committed to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START, you&rsquo;ll join a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation. 

More About START 
START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. START represents the world&rsquo;s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of &ldquo;Hope Through Access&rdquo;. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash; one of the most effective cancer drugs in medical history. 
 Learn more atSTARTresearch.com.  
 Ready to be part of a team changing the future of cancer treatment? 
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online. 
 We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Mon, 23 Mar 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Clinical Research Coordinator - West Valley City, UT]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27774079&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>864a1ea6-8d89-4f1f-bb2e-4eabfb323aad</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. To date, over 45 therapies conducted at START locations have obtained FDA/EMA approval. 
The START Center for Cancer Research is seeking a The Clinical Research Coordinator (CRC) who will work under the guidance of senior research staff to support the daily activities of early phase oncology clinical trials. The CRC ensures the accurate and timely conduct of clinical research, adhering to protocols, regulatory requirements, and patient safety standards. This role involves direct patient interaction, data collection, and maintaining compliance with Good Clinical Practice (GCP). The Clinical Research Coordinator will be assigned multiple protocols at any time for which they will oversee the aspects of assigned protocols with planning and coordinating patient participation in the trial. Also, this role is responsible for implementation as well as completion of protocol specific requirements, providing accurate, up to date information to all team members involved with any aspect of carrying out protocol specific requirements. 
Essential Responsibilities

Communicate on a regular basis with Study Sponsor&rsquo;s, CRO&rsquo;s, staff, etc. regarding questions, concerns, as well as status of the protocol.  
Monitor the overall day-to-day conduct of assigned studies in accordance with the specified protocol requirements, Standard Operating Procedures, and Good Clinical Practice to ensure integrity regarding all aspects of the study.  
Create/review forms created or revised for assigned trials to assure protocol compliance.  
Maintain files using standardized study document labeling and filing procedures.  
Implement initial protocol and amendments, training staff who will be involved in patient treatment and management.  
Maintain an up-to-date contact list.  
Assist with patient screening and determination of eligibility.  
Facilitate the informed consent process ensuring that consent is appropriately completed.  
Prepare and manage source documents according to standard operating procedures.  
Recognize deviations to the protocol and will work with leadership and staff to address corrective actions to prevent deviations.  
Assist data coordinator team with case report form completion and query resolution.  
Work with the Principal Investigator to complete and submit Serious Adverse Event reports.  
Perform protocol specific closeout related activities in conjunction with the data coordinator.  
Provide documentation for all deviations whether related to the protocol or a SOP.  
Ensure that all team members involved understand and adhere to assigned protocols.  
Other duties may be assigned at any time. 

Education & Experience

High School Diploma or GED. 
2 years of clinical research experience. 
Basic understanding of oncology clinical trials, particularly Phase 1 studies. 
Strong attention to detail and accuracy in data collection and documentation. 
Ability to manage multiple tasks and meet deadlines in a fast-paced environment. 
Excellent organizational and time-management skills. 
Strong communication skills, both written and verbal. 
Ability to interact professionally with patients, study staff, and external stakeholders. 
Working knowledge of GCP and regulatory requirements. 
Proficient in Microsoft Office Suite and clinical trial management software. 

Preferred Education and Experience: 

Experience working in an oncology setting. 

Physical and Travel Requirements:

Approximately 80% of time is spent sitting. 
Very fast-paced and ever-changing healthcare environment. 
Demanding deadlines and time frames. 
Constant demand for updating knowledge. 
Works closely with physicians and ancillary personnel in caring for and treating oncology/hematology patients. 

Best-in-Class Benefits and Perks
We value our employees&rsquo; time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:

Comprehensive health coverage: Medical, dental, and vision insurance provided
Robust retirement planning: 401(k) plan available with employer matching
Financial security: Life and disability insurance for added protection
Flexible financial options: Health savings and flexible spending accounts offered
Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided
Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.

More about The START Center for Cancer Research
Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including for 43 therapies that were approved by the FDA. START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. Learn more at STARTresearch.com.
Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.
We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Mon, 23 Mar 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Infusion Nurse - West Valley City, UT]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27774028&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>428fa7e3-e593-4c6a-bc26-b6a20ddda11e</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering "Hope Through Access&rdquo; to cutting edge trials throughout the United States and Europe.  
 We are seeking an Infusion Nurse. The Infusion Nurse is responsible for providing direct patient care to individuals who are participants in research protocols that are conducted at START. The Infusion Nurse uses appropriate professional judgment and decision-making in planning and providing care. Nursing care is to be delivered in a manner consistent with the Standard Operating Procedures and standards of practice, and professional evidence-based standards.
Location: West Valley, UT
Work Schedule:   Monday- Thursday 4 x 10, rotate Fri coverage for 4 hours
Essential Responsibilities:
Patient Care

Administer chemotherapy/immunotherapy/investigational agent to participants (inclusive of parenteral) according to the protocol and applicable regulations.
Perform study-related activities including but not limited to venipuncture, obtaining blood specimens, IV insertion, and venous access device (central line) management, ECG collection, and vital signs.
Collect biological samples according to the protocol and Standard Operating Procedures.
Educate, explain, and inform participants of study procedures.
Record data obtained according to the protocol and Standard Operating Procedures.
Use nursing assessment skills to observe participant general well-being and potential adverse events. Document events and take appropriate action as needed.
Respond to emergency situations based upon nursing standards.
Provide patient education regarding participation in a clinical trial, chemotherapy/immunotherapy/investigational agent administration and potential side effects.
Ensure that the dignity, health, safety, and welfare of participants are given the highest priority at all times.

Planning and problem-solving tasks 

Prepare for clinic day ensuring necessary supplies.
Assist with entry and completion of quality standards for EHR/PQRS.

Communicating tasks 

Assist with the training and mentorship of less tenured staff.
Communicate with providers regarding a change in patient status.
Communicate and interact with peers and other departments in a manner that is viewed as having a positive eect on patient services and sta morale. Interact eectively with patients/family members and demonstrate sensitivity in regards to cultural diversity, age specic needs and condentiality.

 Protocol management tasks 

Work with study team to ensure that study related procedures, drug administration, labs, vital signs and ECG are completed.  

Technical and quality tasks 

Use skills, knowledge, nursing diagnosis, and clinical judgement in order to provide a high standard of care for participants in clinical trials.
Remain current with appropriate emergency certifications and company emergency policy and procedures.
Able to work effectively and efficiently under tight deadlines, high volumes and multiple interruptions.

Education & Experience

High School Diploma or GED.
Licensed Registered Nurse in practicing state.
Basic Life Support (BLS) certification, and AHA certified program.  
Previous experience in peripheral IV insertion and management of venous access device(s).  

Preferred Experience

1 year of experience.
Oncology Certified Nurse (OCN).
Clinical Trial and oncology experience.
Experience working with Microsoft Office, including Teams, Excel and Word.  
Advanced Cardiac Life Support (ACLS) Certification, an AHA certified program.  Can be obtained within 90 days of hire.  
ONS/ONCC Chemotherapy Immunotherapy Certificate&trade;.  Can be obtained within first year of employment.

Best-in-Class Benefits and Perks 
We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package&mdash;based on experience&mdash;along with comprehensive benefits designed to support you both personally and professionally:  

401(k) retirement savings plan with employer match 
Eligibility for an annual performance bonus, based on role and company results 
Generous paid time off and paid holidays 
Comprehensive medical, dental, and vision coverage and optional insurance options 
Companypaid life and disability insurance for added financial protection 
Employee Assistance Program (EAP) providing confidential, nocost support for you and your family from day one 
Flexible FSA and HSA plans to support your financial wellness 
Commitment to a supportive environment that values balance, wellbeing, and flexibility 
We&rsquo;re committed to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START, you&rsquo;ll join a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation. 

More About START 
START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. START represents the world&rsquo;s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of &ldquo;Hope Through Access&rdquo;. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash; one of the most effective cancer drugs in medical history. 
 Learn more atSTARTresearch.com.  
 Ready to be part of a team changing the future of cancer treatment? 
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online. 
 We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Mon, 23 Mar 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Patient Navigator - LOS ANGELES, CA]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27774076&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>5e6443bd-3b48-4c11-9ce2-790b42850f5e</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. To date, over 45 therapies conducted at START locations have obtained FDA/EMA approval. 
The START Center for Cancer Research is seeking a Patient Navigator who will facilitate patient referrals for the START Phase 1 program. This role involves managing referral documentation, monitoring referral metrics, and supporting outreach activities. The Patient Navigator ensures a smooth intake process and efficient communication with referring providers. 
This position is offered at a pay range of $28.00 to $32.00 per hour, based on experience, qualifications, and internal equity. In addition, employees in this role may be eligible for an annual bonus of up to 10% of base earnings.
Essential Responsibilities

Perform referral intake and assist with patient and provider coordination. 
Maintain referral documentation and monitor referral trends. 
Screen patients using EMR systems and genomic platforms for eligibility. 
Support the Nurse Navigator in program outreach and trial promotion. 
Participate in program meetings and contribute to data tracking efforts. 
Other duties may be assigned at any time.   

Education & Experience

High School Diploma or GED. 
Minimum of 2 years of experience in clinical or administrative settings. 
1 year oncology experience. 

Preferred Education and Experience: 

Associate&rsquo;s degree in healthcare or related field. 
Clinical trial experience. 
Strong organizational and communication skills. 

Physical and Travel Requirements:

Limited travel may be required for outreach or program events. 
Must be able to work in a detailed, fast-paced environment. 

Best-in-Class Benefits and Perks
We value our employees&rsquo; time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:

Comprehensive health coverage: Medical, dental, and vision insurance provided
Robust retirement planning: 401(k) plan available with employer matching
Financial security: Life and disability insurance for added protection
Flexible financial options: Health savings and flexible spending accounts offered
Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided
Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.

More about The START Center for Cancer Research
Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including for 43 therapies that were approved by the FDA. START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. Learn more at STARTresearch.com.
Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.
We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Mon, 23 Mar 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Supervisor, Vivarium Operations - San Antonio, TX]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27772950&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>af3b4f0f-8204-4ddd-b3a6-507ad90023ec</guid>
      <description><![CDATA[XenoSTART, the preclinical division of START is a translational research organization focused on creating relevant preclinical cancer models.  Our xenograft models represent each cancer type and disease stage and are established from patients at our domestic and international cancer centers. The XenoSTART Patient-Derived Xenograft (XPDX) platform includes over 2,500 models annotated with each donor patient&rsquo;s cancer treatment and outcome data and characterized using IHC, DNA/RNA sequencing, and relevant in vivo drug efficacy.
Our XPDX models are clinically annotated and include patient treatment history and outcome and are characterized through genomic profiling, histologic analysis, and in vivo drug sensitivity to relevant standards of care. These models may be utilized in the following manner:

In vivo PK/PD and efficacy studies
In vivo efficacy panel screens (indication or target focused)
In licensing of models for internal studies
Custom model development
Orthotopic and radiotherapy studies
Ex vivo and organoid studies

The Supervisor, Vivarium Operations, will play a crucial role in providing an efficient and compliant vivarium. The role includes overseeing daily vivarium processes and team performance, including scheduling, training, and staff evaluation. This role involves performing PDX studies from industry-sponsored and investigator-initiated studies, ensuring adherence to protocols and compliance with all regulatory and safety guidelines, training and scheduling all procedures related to small animal handling, husbandry, surgery, sterile environments, and dosing. This position will also support the optimization of standard operating procedures and working instructions to ensure quality and effectiveness.
 
Essential Responsibilities

Support the Manager, Vivarium in overseeing daily vivarium operations, including supervision of research associates: hiring, onboarding, training, work assignments, time off approval, payroll, performance evaluations, employee development plans, and performance improvement.
Provide training and hands-on study support on technical procedures, including animal handling, dosing, surgery, tumor implantation, euthanasia, sample collection/processing and data entry.
Schedule daily tasks, including resolving conflicts and coordinating efforts across multiple teams.
Create and revise SOPs, working instructions, and other laboratory documentation.
Monitor animal health and maintain accurate records of experiments and results in compliance with institutional and regulatory guidelines.
Ensure the health and welfare of animals to maintain compliance with Association for Assessment and Accreditation of Laboratory Animal Care, International (AAALAC) and Institutional Animal Care and Use Committee (IACUC) standards.
Confirm all study-related documentation is current, accurate, and audit-ready.
Identify and escalate quality or compliance concerns to the appropriate supervisor or project manager.

Education & Experience

Bachelor&rsquo;s degree in animal care or science field.
2-4 years of supervisory experience in an animal facility.
Formal training in animal handling and in vivo research procedures.
Experience with animal handling, dosing, and necropsy procedures.
Familiarity with regulatory requirements and ethical standards for animal research.
Strong communication skills and ability to effectively communicate and present summaries of research results to team members.
Strong organizational skills with great attention to details and ability to troubleshoot problems.

Preferred Education and Experience:

Supervisory experience in a preclinical research setting.
Familiarity with Association for Assessment and Accreditation of Laboratory Animal Care, International (AAALAC), Institutional Animal Care and Use Committee (IACUC), and OSHA compliance.

Physical and Travel Requirements: 

Ability to stand for extended periods of time.
Ability to perform daily tasks requires fine motor skills.
Ability to utilize full range of motion (reaching, bending, etc.).
Ability to lift 40 pounds.
Ability to handle and understand safety procedures associated with biological, investigational, or hazardous materials, not to exceed Biosafety Level 2 (BSL2).
Ability to work with and understand safety procedures associated with Sharps Disposal Containers, including but not limited to needles, scalpel blades, lancets, etc.
Ability to don full Personal Protective Equipment (PPE) on shift, including but not limited to lab coat, gloves, mask, and bouffant.

Best-in-Class Benefits and Perks

We value our employees&rsquo; time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:
Comprehensive health coverage: Medical, dental, and vision insurance provided
Robust retirement planning: 401(k) plan available with employer matching
Financial security: Life and disability insurance for added protection
Flexible financial options: Health savings and flexible spending accounts offered
Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided
Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.

More about The START Center for Cancer Research
Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including for 43 therapies that were approved by the FDA. START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. Learn more at STARTresearch.com.
Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.
We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Mon, 09 Mar 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Auxiliar Documentalista (Contrato Temporal) - Madrid, ES-M]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27772930&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>f3b73838-4d68-48c2-b8d5-c0cb5907c522</guid>
      <description><![CDATA[START Center for Cancer Research (&ldquo;START&rdquo;) es la mayor red mundial de centros de fase I, dedicada por completo a la investigaci&oacute;n cl&iacute;nica oncol&oacute;gica. A lo largo de nuestra historia, START ha proporcionado esperanza a pacientes con c&aacute;ncer en consultas de comunidades globales, ofreci&eacute;ndoles acceso a ensayos de vanguardia en Estados Unidos y Europa. En la actualidad, con m&aacute;s de 1.300 estudios realizados y con centros de investigaci&oacute;n en Estados Unidos y en Espa&ntilde;a, Portugal e Irlanda, la misi&oacute;n de START es acelerar el desarrollo de nuevos medicamentos contra el c&aacute;ncer que mejoren la calidad de vida y la supervivencia de los pacientes con c&aacute;ncer y conduzcan a su eventual curaci&oacute;n. Hasta la fecha, m&aacute;s de 43 terapias realizadas en centros START han obtenido la aprobaci&oacute;n de la FDA/EMA.
Vacante disponible: Auxiliar Documentalista - Ensayos Cl&iacute;nicos Oncol&oacute;gicos (Contrato Temporal)
Responsabilidades:

Preparar la documentaci&oacute;n para las firmas requeridas el d&iacute;a de la visita de inicio 
Revisar la documentaci&oacute;n del investigador de cara a visitas de cierre o auditar&iacute;as
Recepcionar la documentaci&oacute;n de los ensayos cl&iacute;nicos abiertos en la Unidad
Actualizar informaci&oacute;n en las plataformas que apliquen 
Mantener la confidencialidad de la documentaci&oacute;n del ensayo cl&iacute;nico
Gestionar la obtenci&oacute;n de las firmas electr&oacute;nicas de los trainings y de los ensayos abiertos

Requisitos:

Inter&eacute;s en el &aacute;mbito sanitario
Se valorar&aacute; experiencia previa en ensayos cl&iacute;nicos
Persona proactiva y con capacidad de organizaci&oacute;n.
Excelente responsabilidad y atenci&oacute;n al detalle
Habilidad para trabajar en equipo y mantener una buena comunicaci&oacute;n con los compa&ntilde;eros y supervisores.
Nivel de ingl&eacute;s intermedio 

Beneficios

Jornada de Lunes a Viernes
29 d&iacute;as laborables de vacaciones
Retribuci&oacute;n flexible
Posibilidad de realizar clases particulares de ingl&eacute;s totalmente gratuitas
24 y 31 de diciembre libres

&iquest;Est&aacute; preparado para formar parte de un equipo que cambiar&aacute; el futuro del tratamiento del c&aacute;ncer?
&Uacute;nase a nosotros en nuestra misi&oacute;n de vencer al c&aacute;ncer, ensayo cl&iacute;nico a ensayo. Su experiencia y dedicaci&oacute;n pueden ayudarnos a llevar esperanza y curaci&oacute;n a pacientes de todo el mundo. Env&iacute;a tu solicitud en l&iacute;nea.]]></description>
      <pubDate>Sun, 08 Mar 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Infusion Nurse - Grand Rapids, MI]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27772698&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>9dbc60dd-2c3b-45e9-bdc7-25f1846d477b</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largestearly phasesite network, fully dedicated tooncologyclinical research.Throughout ourhistory, START has provided hope to cancer patients inglobalcommunity practices by offering"Hope Through Access&rdquo;tocutting edgetrials throughout the UnitedStatesand Europe. 
 
We are hiring an Infusion Nurse who will be responsible for providing direct patient care to individuals who are participants in research protocols that are conducted at START. The Infusion Nurse uses appropriate professional judgment and decision-making in planning and providing care. Nursing care is to be delivered in a manner consistent with the Standard Operating Procedures and standards of practice, and professional evidence-based standards.
Work Schedule: 7:30 am-6:00 pm EST (4 days a week)
Location: 5800 Foremost Dr. SE, Grand Rapids, MI 49546
Essential Responsibilities
Patient Care

Administer chemotherapy/immunotherapy/investigational agent to participants (inclusive of parenteral) according to the protocol and applicable regulations.
Perform study-related activities including but not limited to venipuncture, obtaining blood specimens, IV insertion, and venous access device (central line) management, ECG collection, and vital signs.
Collect biological samples according to the protocol and Standard Operating Procedures.
Educate, explain, and inform participants of study procedures.
Record data obtained according to the protocol and Standard Operating Procedures.
Use nursing assessment skills to observe participant general well-being and potential adverse events. Document events and take appropriate action as needed.
Respond to emergency situations based upon nursing standards.
Provide patient education regarding participation in a clinical trial, chemotherapy/immunotherapy/investigational agent administration and potential side effects.
Ensure that the dignity, health, safety, and welfare of participants are given the highest priority at all times.

Planning and problem-solving tasks

Prepare for clinic day ensuring necessary supplies.
Assist with entry and completion of quality standards for EHR/PQRS.

Communicating tasks

Assist with the training and mentorship of less tenured staff.
Communicate with providers regarding a change in patient status.
Communicate and interact with peers and other departments in a manner that is viewed as having a positive eect on patient services and sta morale. Interact eectively with patients/family members and demonstrate sensitivity in regard to cultural diversity, age specic needs and condentiality.

Protocol Management tasks

Work with study team to ensure that study related procedures, drug administration, labs, vital signs and ECG are completed. 

Technical and Quality Tasks

Use skills, knowledge, nursing diagnosis, and clinical judgement in order to provide a high standard of care for participants in clinical trials.
Remain current with appropriate emergency certifications and company emergency policy and procedures.
Able to work effectively and efficiently under tight deadlines, high volumes and multiple interruptions.
Other duties may be assigned at any time.


Education & Experience

High School Diploma or GED.
Licensed Registered Nurse in practicing state.
Basic Life Support (BLS) certification, and AHA certified program. 
Previous experience in peripheral IV insertion and management of venous access device(s).   


Preferred Education and Experience:

1 year of experience.
Oncology Certified Nurse (OCN).
Clinical Trial and oncology experience.
Experience working with Microsoft Office, including Teams, Excel and Word. 
Advanced Cardiac Life Support (ACLS) Certification, from an AHA certified program.  Can be obtained within 90 days of hire. 
ONS/ONCC Chemotherapy Immunotherapy Certificate&trade;.  Can be obtained within first year of employment.

Physical & Travel Requirements:

80% of time spent standing and/or walking.
Ability to lift up to a 60-pound weight load.
Very frequent lifting and bending, pushing and/or pulling loads.
Able to perform manual tasks that require the use of ne muscle motor skills.


Best-in-Class Benefits and Perks
We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package&mdash;based on experience&mdash;along with comprehensive benefits designed to support you both personally and professionally: 
Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.


401(k) retirement savings plan with employer match.
Eligibility for an annual performance bonus, based on role and company results 
Generous paid time off and paid holidays 
Comprehensive medical, dental, and vision coverageand optional insuranceoptions 
Company paid life and disability insurance for added financial protection 
Employee Assistance Program (EAP) providing confidential, no cost support for you and your family from day one 
Flexible FSA and HSA plans to support your financial wellness 
Commitment to a supportive environment that values balance, wellbeing, and flexibility 
We&rsquo;recommitted to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START,you&rsquo;lljoin a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation. 



More about The START Center for Cancer Research
START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. STARTrepresentsthe world&rsquo;s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of &ldquo;Hope Through Access&rdquo;.As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash;one ofthe most effective cancerdrugsin medical history. Learn more atSTARTresearch.com. 

Ready to be part of a team changing the future of cancer treatment? 
Join us in our mission to conquer cancer, one clinical trial at a time. Yourexpertiseand dedication can help us bring hope and healing to patients worldwide.Pleasesubmityour application online. 

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Wed, 04 Mar 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Infusion Nurse - Lake Success, NY]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27772712&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>2d811b0c-d2be-4f19-90cc-5cad86a6a9e3</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largestearly phasesite network, fully dedicated tooncologyclinical research.Throughout ourhistory, START has provided hope to cancer patients inglobalcommunity practices by offering"Hope Through Access&rdquo;tocutting edgetrials throughout the UnitedStatesand Europe. 
 
We are hiring an Infusion Nurse who will be responsible for providing direct patient care to individuals who are participants in research protocols that are conducted at START. The Infusion Nurse uses appropriate professional judgment and decision-making in planning and providing care. Nursing care is to be delivered in a manner consistent with the Standard Operating Procedures and standards of practice, and professional evidence-based standards.
This position is offered at a pay range of $55.00 to $75.00 per hour, based on experience, qualifications, and internal equity. In addition, employees in this role may be eligible for an annual bonus of up to 10% of base earnings.
Work Schedule: 8:00 am-5:00 pm EST, Monday-Friday 
Location: 405 Lakeville Road, Entrance A, Lake Success, NY 11042
Essential Responsibilities
Patient Care

Administer chemotherapy/immunotherapy/investigational agent to participants (inclusive of parenteral) according to the protocol and applicable regulations.
Perform study-related activities including but not limited to venipuncture, obtaining blood specimens, IV insertion, and venous access device (central line) management, ECG collection, and vital signs.
Collect biological samples according to the protocol and Standard Operating Procedures.
Educate, explain, and inform participants of study procedures.
Record data obtained according to the protocol and Standard Operating Procedures.
Use nursing assessment skills to observe participant general well-being and potential adverse events. Document events and take appropriate action as needed.
Respond to emergency situations based upon nursing standards.
Provide patient education regarding participation in a clinical trial, chemotherapy/immunotherapy/investigational agent administration and potential side effects.
Ensure that the dignity, health, safety, and welfare of participants are given the highest priority at all times.

Planning and problem-solving tasks

Prepare for clinic day ensuring necessary supplies.
Assist with entry and completion of quality standards for EHR/PQRS.

Communicating tasks

Assist with the training and mentorship of less tenured staff.
Communicate with providers regarding a change in patient status.
Communicate and interact with peers and other departments in a manner that is viewed as having a positive eect on patient services and sta morale. Interact eectively with patients/family members and demonstrate sensitivity in regard to cultural diversity, age specic needs and condentiality.

Protocol Management tasks

Work with study team to ensure that study related procedures, drug administration, labs, vital signs and ECG are completed. 

Technical and Quality Tasks

Use skills, knowledge, nursing diagnosis, and clinical judgement in order to provide a high standard of care for participants in clinical trials.
Remain current with appropriate emergency certifications and company emergency policy and procedures.
Able to work effectively and efficiently under tight deadlines, high volumes and multiple interruptions.
Other duties may be assigned at any time.


Education & Experience

High School Diploma or GED.
Licensed Registered Nurse in practicing state.
Basic Life Support (BLS) certification, and AHA certified program. 
Previous experience in peripheral IV insertion and management of venous access device(s).   


Preferred Education and Experience:

1 year of experience.
Oncology Certified Nurse (OCN).
Clinical Trial and oncology experience.
Experience working with Microsoft Office, including Teams, Excel and Word. 
Advanced Cardiac Life Support (ACLS) Certification, an AHA certified program.  Can be obtained within 90 days of hire. 
ONS/ONCC Chemotherapy Immunotherapy Certificate&trade;.  Can be obtained within first year of employment.

Physical & Travel Requirements:

80% of time spent standing and/or walking.
Ability to lift up to a 60-pound weight load.
Very frequent lifting and bending, pushing and/or pulling loads.
Able to perform manual tasks that require the use of ne muscle motor skills.


Best-in-Class Benefits and Perks
We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package&mdash;based on experience&mdash;along with comprehensive benefits designed to support you both personally and professionally: 
Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.




401(k) retirement savings plan with employer match 






Eligibility for an annual performance bonus, based on role and company results 






Generous paid time off and paid holidays 






Comprehensive medical, dental, and vision coverageand optional insuranceoptions 






Company paid life and disability insurance for added financial protection 






Employee Assistance Program (EAP) providing confidential, no cost support for you and your family from day one 








Flexible FSA and HSA plans to support your financial wellness 






Commitment to a supportive environment that values balance, wellbeing, and flexibility 






We&rsquo;recommitted to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START,you&rsquo;lljoin a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation. 





More about The START Center for Cancer Research
START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. STARTrepresentsthe world&rsquo;s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of &ldquo;Hope Through Access&rdquo;.As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash;one ofthe most effective cancerdrugsin medical history. Learn more atSTARTresearch.com. 

Ready to be part of a team changing the future of cancer treatment? 
Join us in our mission to conquer cancer, one clinical trial at a time. Yourexpertiseand dedication can help us bring hope and healing to patients worldwide.Pleasesubmityour application online. 

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Wed, 04 Mar 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[CTMS Entry Coordinator - Myrtle Beach, SC]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27772726&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>60fd7f65-1675-4be4-8bff-d871ec215d61</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering "Hope Through Access&rdquo; to cutting edge trials throughout the United States and Europe.  
 We are seeking a CTMS Entry Coordinator.  This role will assist the Clinical Research Coordinators in all tasks to support their roles. It will require an understanding of research terminology and basic protocol interpretation. 
Work Schedule: Monday-Friday, 8am-5pm
Location: Myrtle Beach, SC
 Essential Responsibilities

Collect, de-identify, enter/transcribe, and transmit/submit clinical data in paper and/or electronic case reports forms (CRFs), including correction and query resolution for assigned investigational drug studies. This includes but is not limited to images, lab results, and ECGs.  
Collaborate with Clinical Research Coordinator to ensure data timepoints are accurate and provide query resolution.
Contact patients in follow-up as needed per protocol.
Review and utilize protocols as guides for study activities for assigned studies.
Assist with the setup and formatting of study-specific Eligibility, Study Schedules, and Flow Sheets documents per protocol.
Assist with CTMS upkeep, including but not limited to tracking patient visits, IRB re-consents, Serious Adverse Events (SAEs) and Deviations.
Ensure that data transmissions remain current for assigned studies.
Provide support and information to onsite and remote monitors as necessary.
Comply with all applicable regulations, guidelines, and procedures pertaining to data loading, EDC systems, and clinical research.
Share responsibility with Data Coordinators to identify lab facilities and normal lab values used for assigned studies so that lab certifications can be requested for the study file.
Attend meetings regarding assigned studies as needed, including site initiation visits, Roster meetings and Forms Committee.
Communicate as needed with accounts receivable staff regarding transmitted data.

 Required Education and Experience:

High School diploma or equivalent.
One year of research administrative experience within a healthcare, pharmaceutical, or research organization.
Knowledge and training in general office administration skills, including computer applications, filing systems, etc.  
Familiarity with medical terminology.
Strong organizational skills and a sense of timeliness in completing projects.
Must be detail-oriented and able to understand instructions and work independently. 

 Best-in-Class Benefits and Perks 
We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package&mdash;based on experience&mdash;along with comprehensive benefits designed to support you both personally and professionally:   

401(k) retirement savings plan with employer match 
Eligibility for an annual performance bonus, based on role and company results 
Generous paid time off and paid holidays 
Comprehensive medical, dental, and vision coverage and optional insurance options 
Companypaid life and disability insurance for added financial protection 
Employee Assistance Program (EAP) providing confidential, nocost support for you and your family from day one 
Flexible FSA and HSA plans to support your financial wellness 
Commitment to a supportive environment that values balance, wellbeing, and flexibility 
We&rsquo;re committed to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START, you&rsquo;ll join a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation. 

 More About START 
START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. START represents the world&rsquo;s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of &ldquo;Hope Through Access&rdquo;. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash; one of the most effective cancer drugs in medical history. 
 Learn more atSTARTresearch.com.  
 Ready to be part of a team changing the future of cancer treatment? 
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online. 
 We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Wed, 04 Mar 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Farmacéutico - Oncología - Madrid, ES-M]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27772688&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>ff62b791-cb78-4df6-8ca4-dc75a2396790</guid>
      <description><![CDATA[START Center for Cancer Research (&ldquo;START&rdquo;) es la mayor red mundial de centros de fase I, dedicada por completo a la investigaci&oacute;n cl&iacute;nica oncol&oacute;gica. A lo largo de nuestra historia, START ha proporcionado esperanza a pacientes con c&aacute;ncer en consultas de comunidades globales, ofreci&eacute;ndoles acceso a ensayos de vanguardia en Estados Unidos y Europa. En la actualidad, con m&aacute;s de 1.300 estudios realizados y con centros de investigaci&oacute;n en Estados Unidos y en Espa&ntilde;a, Portugal e Irlanda, la misi&oacute;n de START es acelerar el desarrollo de nuevos medicamentos contra el c&aacute;ncer que mejoren la calidad de vida y la supervivencia de los pacientes con c&aacute;ncer y conduzcan a su eventual curaci&oacute;n. Hasta la fecha, m&aacute;s de 43 terapias realizadas en centros START han obtenido la aprobaci&oacute;n de la FDA/EMA.
Vacante disponible: Farmac&eacute;utico - Ensayos Cl&iacute;nicos Oncol&oacute;gicos
Responsabilidades:

 Validaci&oacute;n de tratamientos Onco-Hematol&oacute;gicos
Revisi&oacute;n y registro de interacciones de la medicaci&oacute;n con los f&aacute;rmacos de investigaci&oacute;n, en el screening y durante el tratamiento. 
Revisi&oacute;n de adherencia a los tratamientos de administraci&oacute;n oral 
Realizaci&oacute;n de documentaci&oacute;n espec&iacute;fica por ensayo.
Gesti&oacute;n y control de los medicamentos en investigaci&oacute;n/material fungible usado en los ensayos
Gesti&oacute;n de las visita de monitores
Asesoramiento farmac&eacute;utico a los investigadores, a Enfermer&iacute;a de Investigaci&oacute;n y de tratamiento y a data managers.
Asesoramiento al promotor/monitor de los sistemas de administraci&oacute;n, material de preparaci&oacute;n y sueros disponibles. 
Asistencia a las reuniones semanales con el equipo. 

Cualificaciones y aptitudes

Licenciatura en Farmacia 
Especialidad v&iacute;a FIR en Farmacia Hospitalaria
Valorable experiencia previa en validaci&oacute;n de tratamientos Onco-Hematol&oacute;gicos y ensayos cl&iacute;nicos.
Adecuado manejo de ingl&eacute;s (hablado y escrito)
Debe ser capaz de trabajar bien en un entorno de ritmo r&aacute;pido y ser muy organizado
Excelentes dotes de comunicaci&oacute;n

Beneficios

Jornada de Lunes a Viernes (Festivos y Fines de Semana libres)
30 d&iacute;as laborables de vacaciones
Retribuci&oacute;n flexible
Posibilidad de realizar clases particulares de ingl&eacute;s totalmente gratuitas

&iquest;Est&aacute; preparado para formar parte de un equipo que cambiar&aacute; el futuro del tratamiento del c&aacute;ncer?
&Uacute;nase a nosotros en nuestra misi&oacute;n de vencer al c&aacute;ncer, ensayo cl&iacute;nico a ensayo. Su experiencia y dedicaci&oacute;n pueden ayudarnos a llevar esperanza y curaci&oacute;n a pacientes de todo el mundo. Env&iacute;a tu solicitud en l&iacute;nea.]]></description>
      <pubDate>Tue, 03 Mar 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Pharmacy Technician - Lake Success,, NY]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27772632&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>f8ee8279-b300-4535-b92a-3c661a90f811</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largestearly phasesite network, fully dedicated tooncologyclinical research.Throughout ourhistory, START has provided hope to cancer patients inglobalcommunity practices by offering"Hope Through Access&rdquo;tocutting edgetrials throughout the UnitedStatesand Europe. 

The Pharmacy Technician will assure safe, efficient, and cost-effective preparation of chemotherapy, biologic therapy, and supportive care medications for administration to patients following all applicable regulations. Also, this role will work collaboratively with Site Leaders and Pharmacists to maintain adequate and cost-effective inventory of drugs and supplies. The hourly rate for this role is $28 -$31/hour. Your compensation may vary based on your unique qualifications, experience, and market factors.
Work Schedule: 7:30 am-4:00 pm EST
Location: 450 Lakeville Road, Entrance A, Lake Success, NY 11042
Essential Responsibilities

Mix and label chemotherapy, biologic therapy and supportive care medications. 
Perform proper procedures and documentation in inventory management systems during the fulfillment of the medication order. 
Prepare parenteral dosage forms utilizing aseptic techniques in accordance with departmental policies, standards set forth in current USP, state & federal regulations and GCP guidelines for investigational medications. 
Prepare and deliver medication ensuring proper storage location requirements are met based on the stability needs of the product. 
Perform routine weekly inventory and quality assurance tasks, including checking extemporaneously manufactured medications, commercially available medications, I.V. solutions and equipment for expiration dates, recalls, or signs of deterioration. 
Receive medication and supplies in accordance with inventory control and purchasing policies. Help to maintain all medication inventory levels within the predetermined stocking level, calling attention to needs for revision, or perpetual supply problems. 
Interact with study monitors by providing drug accountability reports and temperature storage logs. Facilitate monitor verification of inventory, training and other GCP documentation. 
Maintain and generate reports through the applicable computer programs.  

 Education & Experience

High School Diploma/GED. 
At least 2 years of experience preparing chemotherapy and biologic therapies. 
Current State registration as a pharmacy technician (CPhT). 

 Physical & Travel Requirements:

80% of time spent standing and/or walking. 
Ability to lift up to a 25-pound weight load.Some lifting and bending, pushing and/or pulling loads. 


Best-in-Class Benefits and Perks
We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package&mdash;based on experience&mdash;along with comprehensive benefits designed to support you both personally and professionally: 




 


401(k) retirement savings plan with employer match 






Eligibility for an annual performance bonus, based on role and company results 






Generous paid time off and paid holidays 






Comprehensive medical, dental, and vision coverageand optional insuranceoptions 






Company  paid life and disability insurance for added financial protection 






Employee Assistance Program (EAP) providing confidential, no cost support for you and your family from day one 








Flexible FSA and HSA plans to support your financial wellness 






Commitment to a supportive environment that values balance, wellbeing, and flexibility 






We&rsquo;recommitted to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START,you&rsquo;lljoin a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation. 







More about START
START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. STARTrepresentsthe world&rsquo;s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of &ldquo;Hope Through Access&rdquo;.As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash;one ofthe most effective cancerdrugsin medical history. 

Learn more atSTARTresearch.com. 


Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Tue, 03 Mar 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Enfermero/a de Investigación - Study Coordinator - Barcelona, ES-B]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27772687&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>4f8376bf-9f85-42a5-aec8-c8de1c61dc51</guid>
      <description><![CDATA[START Center for Cancer Research (&ldquo;START&rdquo;) es la mayor red mundial de centros de fase I, dedicada por completo a la investigaci&oacute;n cl&iacute;nica oncol&oacute;gica. A lo largo de nuestra historia, START ha proporcionado esperanza a pacientes con c&aacute;ncer en consultas de comunidades globales, ofreci&eacute;ndoles acceso a ensayos de vanguardia en Estados Unidos y Europa. En la actualidad, con m&aacute;s de 1.300 estudios realizados y con centros de investigaci&oacute;n en Estados Unidos y en Espa&ntilde;a, Portugal e Irlanda, la misi&oacute;n de START es acelerar el desarrollo de nuevos medicamentos contra el c&aacute;ncer que mejoren la calidad de vida y la supervivencia de los pacientes con c&aacute;ncer y conduzcan a su eventual curaci&oacute;n. Hasta la fecha, m&aacute;s de 43 terapias realizadas en centros START han obtenido la aprobaci&oacute;n de la FDA/EMA.
Vacante disponible: Enfermero/a de Investigaci&oacute;n - Study Coordinator
Responsabilidades:

Identificar los requisitos de los Ensayos cl&iacute;nicos Fase I, incluyendo objetivos, cohortes y necesidades en el cuidado del paciente. 
Asegurar la validez de los datos obtenidos en los documentos fuente
Cumplir con la pol&iacute;tica de env&iacute;os y manipulaci&oacute;n de muestras biol&oacute;gicas
Proporcionar toda la informaci&oacute;n necesaria sobre el ensayo cl&iacute;nico desde el inicio del mismo, as&iacute; como enmiendas posteriores al resto del equipo de investigaci&oacute;n. 
Participar en las Visitas de Inicio.
Realizar todos los trainings que sean necesarios para poner en marcha el ensayos cl&iacute;nico en la Unidad.
Educar al paciente sobre los procedimientos y efectos secundarios relacionados con el ensayo cl&iacute;nico y el/los f&aacute;rmaco/sen investigaci&oacute;n.
Asegurar que el proceso de obtenci&oacute;n del consentimiento informado cumple con las normativas de la AEMPS, GCP, promotor y CEIm
Colaborar con el Investigador para determinar la elegibilidad de un paciente para participar en un ensayo cl&iacute;nico, incluyendo la documentaci&oacute;n necesaria con los criterios de inclusi&oacute;n/exclusi&oacute;n que especifica el protocolo
Garantizar la adhesi&oacute;n al esquema del protocolo de los eventos y requerimientos (queries).
Realizar las llamadas de seguimiento/seguridad/supervivencia a los pacientes seg&uacute;n protocolo, una vez el paciente finalice el tratamiento en ensayo, durante el periodo que se requiera seg&uacute;n protocolo.

Requisitos:

Titulaci&oacute;n de Enfermer&iacute;a
Inter&eacute;s en el &aacute;mbito sanitario
Persona proactiva y con capacidad de organizaci&oacute;n.
Excelente responsabilidad y atenci&oacute;n al detalle
Habilidad para trabajar en equipo y mantener una buena comunicaci&oacute;n con los compa&ntilde;eros y supervisores.
Nivel de ingl&eacute;s intermedio.

&iquest;Est&aacute; preparado para formar parte de un equipo que cambiar&aacute; el futuro del tratamiento del c&aacute;ncer?
&Uacute;nete a nosotros en nuestra misi&oacute;n de vencer al c&aacute;ncer, ensayo cl&iacute;nico a ensayo. Tu experiencia y dedicaci&oacute;n pueden ayudarnos a llevar esperanza y curaci&oacute;n a pacientes de todo el mundo. Env&iacute;a tu solicitud en l&iacute;nea.]]></description>
      <pubDate>Tue, 03 Mar 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Financial & Operations Analyst (Remote) - San Antonio, TX]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27772362&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>b05cf17f-cfe1-46a6-9013-77a6592f3b3d</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering access to cutting edge trials throughout the US and Europe. Today, with over 1,300 studies completed, and with research facilities in the United States and in Spain, Portugal, and Ireland, START&rsquo;s mission is to accelerate the development of new anticancer drugs that will improve the quality of life and survival for patients with cancer and lead to its eventual cure. To date, over 43 therapies conducted at START locations have obtained FDA/EMA approval. Incredibly, while Academic Medical Centers (AMCs) conduct 80% of cancer trials, such trials reach only 20% of the patient population &ndash; leaving the majority of patients who are treated in community practices and hospitals without access to a clinical trial when their care journey calls for one. START serves the many &ndash; by bringing cancer trials to physicians and their patients in community hospitals and practices when hope is needed most.
 
START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash; the most effective cancer drug in medical history.

We are hiring a motivated Financial & Operations Analyst who will report to the Director, Finance &ndash; Operations and play a critical role in strengthening the partnership between Finance and Operations. This role will provide accurate, timely, and actionable insights that support operational efficiency, profitability, and strategic decisionmaking across START&rsquo;s clinic network and joint ventures. The position supports both recurring operational reporting and higher-level strategic analysis during periods of rapid growth and expansion. will be responsible for overseeing the accounts payable process, ensuring accurate and timely processing of invoices, and payments to vendors. 
This is a remote role. The annual base salary for this role is $80,000 - $90,000. However, base pay may vary depending on multiple individualized factors including market location, job-related knowledge, skills, and experience. 
Essential Responsibilities
Capacity Modeling & Operational Analytics
&middot;       Distribute monthly reports highlighting group and individual efficiency, along with variance to benchmark performance.
&middot;       Maintain and continuously improve capacity models across US, EU, Late Phase, Pediatrics, and Central Operations.
&middot;       Advance current models toward greater automation, standardization, and frequency.
&middot;       Analyze clinic throughput, sitelevel performance, and operational bottlenecks to identify improvement opportunities.
Business Reviews & Operational Visibility
&middot;       Prepare monthly and quarterly business review materials for clinics, departments, and sponsorfacing teams (Regulatory, Study StartUp, Procurement, etc.).
&middot;       Prepare analytical packages to support leadership decisionmaking on investments, new sites, resource allocation, and operational improvement initiatives.
Joint Venture (JV) Support & Financial Reporting
&middot;       Prepare monthly and quarterly JV reporting packages, including highlevel metrics, financial statements, and variance analyses.
&middot;       Support JV meetings by ensuring materials are complete, accurate, and delivered on time; attend or run meetings as needed.
&middot;       Respond to partner and internal stakeholder requests for financial data, insights, and analysis.
CrossFunctional Collaboration
&middot;       Serve as a bridge between Finance and Operations, ensuring shared understanding of financial drivers, constraints, and opportunities.
&middot;       Partner with clinic and departmental leaders to identify risks, trends, and areas requiring deeper review. 
&middot;       Support development, enhancement, and maintenance of Power BI dashboards used across Finance and Operations.
&middot;       Other duties may be assigned at any time. 
Required Education and Experience: 
&middot;       Bachelor&rsquo;s degree in Finance, Accounting, Economics, Data Analytics, or related field.
&middot;       2&ndash;5 years of financial analysis, operations analysis, or related analytical experience.
&middot;       Advanced Excel skills; strong proficiency in data modeling and scenario-based analysis.
&middot;       Experience with BI tools (Power BI strongly preferred).
&middot;       Strong attention to detail with the ability to synthesize complex data into clear insights.
&middot;       Ability to manage multiple priorities in a fast-paced, evolving environment.
Preferred Education and Experience:
&middot;       Experience in healthcare, clinical research, or multi-site operational environments.
&middot;       Familiarity with ERP or planning tools (NetSuite, Adaptive Planning).
&middot;       Ability to automate repetitive reporting processes.
&middot;       Comfort interacting with senior leadership and external partners.
Physical & Travel Requirements:
&middot;       Travel: Required to travel up to 20% of the time
&middot;       Sitting: Must be able to sit for extended periods of time. 
&middot;       Standing: Must be able to stand for extended periods of time.  
&middot;       Bending: Must be able to reach overhead, at shoulder level, or bend to perform tasks. 
Best-in-Class Benefits and Perks
We value our employees&rsquo; time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:
&middot;       Comprehensive health coverage: Medical, dental, and vision insurance provided
&middot;       Robust retirement planning: 401(k) plan available with employer matching
&middot;       Financial security: Life and disability insurance for added protection
&middot;       Flexible financial options: Health savings and flexible spending accounts offered
&middot;       Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided
&middot;       Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.

More about The START Center for Cancer Research
Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including for 43 therapies that were approved by the FDA. START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. Learn more at STARTresearch.com.

Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Fri, 27 Feb 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Senior Manager, Study Activation (EU)  - Madrid, ES-M]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27772255&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>37d6acf3-b30f-48b6-9311-8474b0947dc5</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering access to cutting edge trials throughout the US and Europe. Today, with over 1,300 studies completed, and with research facilities in the United States and in Spain, Portugal, and Ireland, START&rsquo;s mission is to accelerate the development of new anticancer drugs that will improve the quality of life and survival for patients with cancer and lead to its eventual cure.
 
START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash; the most effective cancer drug in medical history.
We are seeking a Senior Manager, Study Activation (EU) 


Essential Responsibilities:  




Supports SSU strategy in close collaboration with the VP, Client Engagement & Study Activation 






Collaborates with central services and site-level study team to ensure SSU timelines and deliverables are met according to internal process, KPIs, and Sponsor goals 






Accountable for timely start-up activities until Green Light (ready to initiate site millstone)  






Supports study feasibility and site selection milestones in close collaboration with Pre-Award Team as well as the site-level study team. 






Supports and directs all study activation milestones in close collaboration with Study Start-up Specialist as well as the site-level study team. 






Serves as main contact for issues in SSU phases, escalating as necessary 






Ensures sites are prepared for "Green Light" and ensures all documentation is in place for initial and subsequent drug release. Responsible for review and sign off of the site "Green Light" 






Oversees EU SSU team activities to achieve start-up timelines and quality execution, (proposing and implementing corrective actions where appropriate), according to START standards  






Leads EU SSU team meetings and participates in network study team meetings, as required 






Contribute to the growth and development of departmental staff, processes and systems. 






Ability to embrace HubSpot, Veeva Vault, FileMaker, and CTMS system and associated functionality and maintain records related to specific area of assignment 








Assist with in-service trainings and new hire trainings for staff 






Assist with special projects as assigned.  This includes, but is not limited to, conducting research, preparing presentations and documents as requested 






Serves as a back to the VP and departmental team, when needed 






Perform additional duties as assigned 




Required Education and Experience: 




BA/BS degree with at least 5 years of experience in pharmaceutical related drug development or direct equivalent experience or advanced degree   






Must have knowledge of clinical trial conduct, including, multi-center, global trials. 






Experience within the EU-CTR 






Must have strong knowledge of ICH/GCP guidelines and regulatory requirements.  






Requires proven project management skills and leadership ability  






Must have excellent interpersonal, written and verbal communication skills, administrative skills and computer ability.  






Experience in working cross functionally and with external providers  






Experience with development & implementation of process improvement related initiatives  






Global Experience with site activation activities including submission requirements.  




Travel Requirements: 




Travel: Required to travel up to 20% of the time  






Approximately 80% of time is spent sitting. 






Very fast-paced and ever-changing healthcare environment. 








Demanding deadlines and time frames. 






Constant demand for updating knowledge 




 Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.]]></description>
      <pubDate>Wed, 25 Feb 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Clinical Data Entry Coordinator - Grand Rapids, MI]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27771109&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>2720b7f4-005e-4023-b481-40b9239f7419</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering access to cutting edge trials throughout the US and Europe. Today, with over 1,300 studies completed, and with research facilities in the United States and in Spain, Portugal, and Ireland, START&rsquo;s mission is to accelerate the development of new anticancer drugs that will improve the quality of life and survival for patients with cancer and lead to its eventual cure. To date, over 43 therapies conducted at START locations have obtained FDA/EMA approval. Incredibly, while Academic Medical Centers (AMCs) conduct 80% of cancer trials, such trials reach only 20% of the patient population &ndash; leaving the majority of patients who are treated in community practices and hospitals without access to a clinical trial when their care journey calls for one. START serves the many &ndash; by bringing cancer trials to physicians and their patients in community hospitals and practices when hope is needed most.
 
START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash; the most effective cancer drug in medical history.

We are hiring a motivated Clinical Data Entry Coordinator for our Grand Rapids, MI location, who will collect, enter/transcribe, and transmit/submit clinical data for assigned investigational drug studies. 
Essential Responsibilities

Collect, enter/transcribe, and transmit/submit clinical data in paper and/or electronic case report forms (CRFs), including correction and query resolution for assigned investigational drug studies.
Receive and request patient records/data from the study team as required to complete CRFs for assigned studies. 
Review patient data for completeness and accuracy for assigned studies.
Coordinate and schedule monitor visits for assigned studies.  This includes exit meetings with monitors to review data or queries.
Identify lab facilities used for assigned studies and communicate to the Regulatory Affairs staff so that lab certifications can be requested for the study file.
Review and utilize protocols as guides for study activities for assigned studies.
Assure that data entry remains current for all assigned studies.
Attend meetings as required for assigned studies.  This includes, but is not limited to, site initiation meetings, monitor exit meetings, close-out visit meetings, and audit preparation meetings.
Be available and on-site, if required, during audits for assigned studies.
Communicate as needed with accounts receivable staff regarding submitted data. 

Education & Experience

Bachelor&rsquo;s degree or equivalent experience in lieu of degree. 
Knowledge and training in general office administration skills, including computer applications, filing systems, etc.

Preferred Education and Experience

Ability to accurately perform data review and CRF completion in its entirety with minimal direction. 
Familiarity with medical terminology.
Additional demonstration of clinical research knowledge as evidenced by the use of either CCRP or CCRC credentials is highly desirable. 

Best-in-Class Benefits and Perks
We value our employees&rsquo; time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:

Comprehensive health coverage: Medical, dental, and vision insurance provided
Robust retirement planning: 401(k) plan available with employer matching
Financial security: Life and disability insurance for added protection
Flexible financial options: Health savings and flexible spending accounts offered
Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided
Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.


More about The START Center for Cancer Research
Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including for 43 therapies that were approved by the FDA. START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. Learn more at STARTresearch.com.

Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Tue, 10 Feb 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[In Vivo Research Assistant - San Antonio, TX]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27771057&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>69712592-2f0c-4739-8b6a-950351cc574b</guid>
      <description><![CDATA[XenoSTART, the preclinical division of START is a translational research organization focused on creating relevant preclinical cancer models.  Our xenograft models represent each cancer type and disease stage and are established from patients at our domestic and international cancer centers. The XenoSTART Patient-Derived Xenograft (XPDX) platform includes over 2,500 models annotated with each donor patient&rsquo;s cancer treatment and outcome data and characterized using IHC, DNA/RNA sequencing, and relevant in vivo drug efficacy.
Our XPDX models are clinically annotated and include patient treatment history and outcome and are characterized through genomic profiling, histologic analysis, and in vivo drug sensitivity to relevant standards of care. These models may be utilized in the following manner:
In vivo PK/PD and efficacy studies

In vivo efficacy panel screens (indication or target focused)
In licensing of models for internal studies
Custom model development
Orthotopic and radiotherapy studies
Ex vivo and organoid studies

 We are hiring a motivated In Vivo Research Assistant.  Under direct supervision of the supervisor, this position involves collection of data obtained from industry sponsored and investigator-initiated studies. In addition, this position entails all procedures involved with small animal handling, husbandry, surgery, drug preparation and dosing and other related duties for the START Preclinical Group.
Essential Responsibilities

Collect internally generated data including small animal body weights and tumor dimensions using mechanical and electronic devices and stores on internal server. 
Perform day-to-day procedures including but not limited to small animal handling, husbandry, surgery, anesthesia, cell culture, blood and tissue collection and processing, tumor implantation, cell injection, euthanasia, sample processing including cryopreservation, cryofreezing and fixation, sterilization, maintenance and cleaning. These operations may involve multi-tasking, lifting of greater than forty pounds, standing or sitting for long periods of time and repetitive procedures. 
Prepare, aliquot and properly store vehicles, drugs, media and other laboratory solutions. 
Administer agents by various routes on various dosing schedules. 
Attend regular meetings and briefings regarding preclinical studies as required. 
Assist in animal and laboratory activities as needed. 
Assist in data preparation and administrative log management as needed. 
Follow all Standard Operating Procedures (SOPs). 

Education & Experience

High school diploma/GED.
Minimum of 1 year of similar experience.
Must be familiar with Microsoft Office applications.
Attention to detail.
Ability to work in a fast-paced team environment.

Preferred Education and Experience:

Bachelor&rsquo;s degree.
Knowledge and training in animal handling and research.

Best-in-Class Benefits and Perks
We value our employees&rsquo; time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:

Comprehensive health coverage: Medical, dental, and vision insurance provided
Robust retirement planning: 401(k) plan available with employer matching
Financial security: Life and disability insurance for added protection
Flexible financial options: Health savings and flexible spending accounts offered
Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided
Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.


More about The START Center for Cancer Research
Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including for 43 therapies that were approved by the FDA. START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. Learn more at STARTresearch.com.

Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.

We are an equal opportunity employer that welcomes and encourages diversity]]></description>
      <pubDate>Mon, 09 Feb 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Enfermero/a - Oncología - La Rioja, LO]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27770757&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>7f1279d5-92ea-4a00-a995-94c1d6b39e81</guid>
      <description><![CDATA[START Center for Cancer Research (&ldquo;START&rdquo;) es la mayor red mundial de centros de fase I, dedicada por completo a la investigaci&oacute;n cl&iacute;nica oncol&oacute;gica. A lo largo de nuestra historia, START ha proporcionado esperanza a pacientes con c&aacute;ncer en consultas de comunidades globales, ofreci&eacute;ndoles acceso a ensayos de vanguardia en Estados Unidos y Europa. En la actualidad, con m&aacute;s de 1.300 estudios realizados y con centros de investigaci&oacute;n en Estados Unidos y en Espa&ntilde;a, Portugal e Irlanda, la misi&oacute;n de START es acelerar el desarrollo de nuevos medicamentos contra el c&aacute;ncer que mejoren la calidad de vida y la supervivencia de los pacientes con c&aacute;ncer y conduzcan a su eventual curaci&oacute;n. Hasta la fecha, m&aacute;s de 43 terapias realizadas en centros START han obtenido la aprobaci&oacute;n de la FDA/EMA.
Vacante disponible: Enfermero/a de Tratamiento- Ensayos Cl&iacute;nicos Oncol&oacute;gicos
Responsabilidades:

Promover el cumplimiento de los procedimientos necesarios requeridos por el ensayo cl&iacute;nico.
Colaborar con el equipo de investigaci&oacute;n para mejorar los procedimientos realizados al paciente desde su inclusi&oacute;n hasta la finalizaci&oacute;n del ensayo cl&iacute;nico.
Tomar las constantes vitales, peso, talla y realizar todos los procedimientos necesarios requeridos por el protocolo del ensayo cl&iacute;nico.
Administrar los tratamientos de acuerdo con el protocolo y los requisitos normativos.
Recoger muestras de sangre, suero y/u orina de los pacientes para el laboratorio cl&iacute;nico seg&uacute;n lo requiera el protocolo.
Extraer, procesar y enviar muestras de Farmacocin&eacute;tica (PK)/Farmacodinamia.

Requisitos

Inter&eacute;s en Ensayos Cl&iacute;nicos
Capacidad creativa para la resoluci&oacute;n de problemas; habilidad para navegar a trav&eacute;s de complejos protocolos oncol&oacute;gicos de fase I y aplicarlos a la misi&oacute;n de START de recopilaci&oacute;n de datos de calidad.
Persona proactiva y con capacidad de organizaci&oacute;n.
Habilidad para trabajar en equipo y mantener una buena comunicaci&oacute;n con los compa&ntilde;eros y supervisores.

Formaci&oacute;n

Licenciatura en Enfermer&iacute;a
Colegiatura en Enfermer&iacute;a

&iquest;Est&aacute; preparado para formar parte de un equipo que cambiar&aacute; el futuro del tratamiento del c&aacute;ncer?
&Uacute;nase a nosotros en nuestra misi&oacute;n de vencer al c&aacute;ncer, ensayo cl&iacute;nico a ensayo. Su experiencia y dedicaci&oacute;n pueden ayudarnos a llevar esperanza y curaci&oacute;n a pacientes de todo el mundo. Env&iacute;e su solicitud en l&iacute;nea.]]></description>
      <pubDate>Tue, 03 Feb 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Study Activation - Clinical Trials (Temporal) - Madrid, ES-M]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27770651&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>6734c403-b08f-4181-ae3f-12d3eb2b1587</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering access to cutting edge trials throughout the US and Europe. Today, with over 1,300 studies completed, and with research facilities in the United States and in Spain, Portugal, and Ireland, START&rsquo;s mission is to accelerate the development of new anticancer drugs that will improve the quality of life and survival for patients with cancer and lead to its eventual cure. To date, over 43 therapies conducted at START locations have obtained FDA/EMA approval. Incredibly, while Academic Medical Centers (AMCs) conduct 80% of cancer trials, such trials reach only 20% of the patient population &ndash; leaving the majority of patients who are treated in community practices and hospitals without access to a clinical trial when their care journey calls for one. START serves the many &ndash; by bringing cancer trials to physicians and their patients in community hospitals and practices when hope is needed most.
 
START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash; the most effective cancer drug in medical history.

We are hiring a: Pre &ndash; Award Coordinator (Study Activation)

Essential Responsibilities:

Perform all pre-award activities from time of initial contact to official site selection for the START Europe sites.
Review, respond, and maintain the central email inbox for new study opportunities.
Facilitate all pre-award related meetings, including but not limited to, Protocol Review and Development Committee meetings, Pre-Study Site Visits, weekly Study Start-Up Status meetings, and Sponsor/Investigator meetings for the START Europe sites.
Coordinate facility tours prior to official site selection.
Support execution of the Sponsor/CRO required site feasibility questionnaires for the START Europe sites when applicable and ensuring the questionnaire are completed accurately and in a timely manner.
Work within the forecasted timelines in accordance with Sponsor/CRO expectations and ensure they are met; if forecasted timelines are not reached, provide clear rationale for delays and contingency plans to mitigate impact.
Review and comply with Standard Operating Procedures and pre-award processes in a timely manner and ensure all relevant documents are submitted to Sponsor/CRO and the Investigational Site File (ISF).
Anticipate and identify issues during pre-award process, resolve minor to moderate issues independently, and escalate complex issues.


Maintain and ensure data tracking systems are updated with pre-award milestones.
Assist with in-service trainings and new hire trainings for staff.
Assist with special projects as assigned.  This includes, but is not limited to, conducting research, preparing presentations and documents as requested.


Other duties may be assigned at any time.


Required Education and Experience:

High school diploma or equivalent.
At least two years&rsquo; experience in administrative setting Proficient working knowledge of word processing, spreadsheet, database, and presentation software (MS Office skills such as Outlook, Word, Excel, PowerPoint, and SharePoint).
Excellent written and oral communication skills, as well as time management skills.
Demonstrated ability to work in a dynamic environment under compressed deadlines across several projects, each with unique requirements.



More about The START Center for Cancer Research
Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including for 43 therapies that were approved by the FDA. START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. Learn more at STARTresearch.com.

Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Mon, 02 Feb 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Clinical Trainer, Integrations (Remote) - San Antonio, TX]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27769809&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>6bcfe048-4e48-4837-926b-ba2f70ebd045</guid>
      <description><![CDATA[The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. To date, over 45 therapies conducted at START locations have obtained FDA/EMA approval. 
The START Center for Cancer Research is seeking a Clinical Trainer, Integrations to join the Integration team and lead the rollout of new START locations in the US and internationally. This role is responsible for managing the end-to-end integration process for new clinical sites, with a particular emphasis on onboarding and training all new clinical team members&mdash;including nursing, research coordinators, and scheduling teams. The Clinical Trainer will collaborate closely with Operations, Training, Quality Assurance and other central service departments to ensure seamless site launches, consistent high-quality patient care, and adherence to project timelines and standards.
The ideal candidate will demonstrate strong project management skills, experience with onboarding and training multidisciplinary teams, and proficiency with project management tools and regular progress reporting.
This is a remote role. The annual base salary for this role is $80,000 - $120,000. However, base pay may vary depending on multiple individualized factors including market location, job-related knowledge, skills, and experience. A 10% annual performance bonus is offered as well.
Essential Responsibilities

Lead the planning, coordination and execution of clinical training for each new early-phase clinical oncology research location
Collaborate closely with Training and Quality departments to build comprehensive onboarding and training programs for all new clinical team members, including nursing, research coordinators and scheduling staff
Oversee and facilitate onboarding and training programs for clinical team members for new sites
Develop and document new clinical workflows as needed and incorporate into training
Develop and implement project plans, timelines, and deliverables, ensuring all integration milestones are met
Utilize project management tools to track progress, manage tasks, and generate regular status reports for leadership and stakeholders
Monitor and report on integration progress, identifying risks and proactively addressing challenges to ensure successful site launches
Collaborate with leadership and multidisciplinary teams to ensure operational readiness and alignment with organizational goals
Travel to new and existing START locations to oversee onboarding, training, and process implementation

Education & Experience

Education: Bachelor&rsquo;s degree in a healthcare, science, business, or related field. RN license is a plus but not required
Certifications: Project management certification (e.g., PMP, CAPM) preferred but not required
Experience:

Minimum of 3 years of experience in project management, clinical operations, or healthcare integration, preferably in oncology, research, or a related clinical setting
Experience facilitating the onboarding and training multidisciplinary clinical teams
Experience with the M365 suite including Excel and PowerPoint and experience with Smartsheet or other project management tools is preferred



Physical and Travel Requirements:

Required to travel up to 50% of the year, including travel to new clinic locations across the US
Physical Demands:

Sitting: Frequent, for administrative and training duties
Standing: Frequent, during training and setup activities
Bending: Occasional, for equipment setup or process implementation
Lifting: Ability to lift up to 25 pounds, occasionally, for handling supplies and equipment
Exposure to clinical environments, including areas where protective precautions are necessary



Best-in-Class Benefits and Perks
We value our employees&rsquo; time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:

Comprehensive health coverage: Medical, dental, and vision insurance provided
Robust retirement planning: 401(k) plan available with employer matching
Financial security: Life and disability insurance for added protection
Flexible financial options: Health savings and flexible spending accounts offered
Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided
Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.

More about The START Center for Cancer Research
Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including for 43 therapies that were approved by the FDA. START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. Learn more at STARTresearch.com.
Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.
We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Tue, 20 Jan 2026 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Oncology/Urology NP/PA - Myrtle Beach, SC]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27768232&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>461B09AD-E632-206C-E063-0100007FD2A9</guid>
      <description><![CDATA[The START Center for Cancer Research ("START") is the world's largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering access to cutting edge trials throughout the US and Europe. Learn more at STARTresearch.com.
Join Our Pioneering Team as an Advanced Practice Provider (APP) &ndash; Urology and Later Phase Clinical Research Program
Location: 823 82nd Pkwy, Suite B, Myrtle Beach, South Carolina 29572 - We offer willing to offer relocation assistance for the right fit!
The Advanced Practice Provider (APP) &ndash; Urology and Later Phase Clinical Research Program supports clinical care and protocol execution for urology-focused and later-phase oncology clinical trials. Operating as a sub-investigator under the supervision of the Principal Investigator (PI), the APP supports patient screening, study visits, and continuity of care while facilitating efficient clinic operations within a disease-focused research environment.
Schedule: Our clinic is open Monday through Friday from 8-5. We can be flexible with the schedule if a four day work week is preferred.
Essential Responsibilities:

Serve as a sub-investigator on assigned urology and later-phase clinical trials following completion of required training and delegation documentation.
Conduct protocol-required physical examinations and study visits for patients in screening, on treatment, and in follow-up as delegated by the Principal Investigator.
Prepare medical histories and clinical summaries in advance of new patient consults to support efficient PI evaluation.
Assist with patient screening activities, including chart review, protocol feasibility assessment, and coordination of required evaluations.
Support post-consent screening and ongoing study assessments in accordance with protocol requirements.
Assist with adverse event (AE) and serious adverse event (SAE) identification, documentation, and follow-up in collaboration with the Principal Investigator and research team.
Serve as a primary clinical contact for the research care team for routine patient management questions and escalate complex issues to the Principal Investigator.
Coordinate closely with nursing, clinical research coordinators, and ancillary services to support protocol adherence and patient-centered care.
Support disease-focused outreach, education, and multidisciplinary collaboration as requested.
Other duties may be assigned at any time.

Education & Experience:

Advanced practice degree (Nurse Practitioner or Physician Assistant) with current licensure in the state of South Carolina or ability to be licensed in the state of South Carolina.
Minimum of 3 to 5 years of experience in urology, oncology, or clinical research.

Preferred Education and Experience:

Master's degree or Doctoral degree in advanced practice nursing or physician assistant studies.
National certification as a Nurse Practitioner or Physician Assistant. Eligibility and willingness to serve as a sub-investigator on clinical trials.
Prior experience in urology clinical care or later-phase oncology clinical research.

Physical & Travel Requirements:

Travel: Limited travel may be required during training and onboarding.
Sitting: Must be able to sit for extended periods of time.
Standing: Must be able to stand for extended periods of time.
Bending: Must be able to reach overhead, at shoulder level, or bend to perform tasks.
Lifting: Must be able to lift up to 25 pounds.
Exposure: Works closely with physicians, research staff, and ancillary personnel in caring for and treating urology and oncology patients.

Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.]]></description>
      <pubDate>Tue, 16 Dec 2025 00:00:00 EST</pubDate>
    </item>
    <item>
      <title><![CDATA[Director of Business Development (Remote) - San Antonio, TX]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27758101&amp;companyGK=51234&amp;portalGK=41776</link>
      <guid>3844D628-E734-3635-E063-0100007F1605</guid>
      <description><![CDATA[XenoSTART, the preclinical division of START is a translational research organization focused on creating relevant preclinical cancer models.  Our xenograft models represent each cancer type and disease stage and are established from patients at our domestic and international cancer centers. The XenoSTART Patient-Derived Xenograft (XPDX) platform includes over 2,500 models annotated with each donor patient&rsquo;s cancer treatment and outcome data and characterized using IHC, DNA/RNA sequencing, and relevant in vivo drug efficacy.

Our XPDX models are clinically annotated and include patient treatment history and outcome and are characterized through genomic profiling, histologic analysis, and in vivo drug sensitivity to relevant standards of care. These models may be utilized in the following manner:

In vivo PK/PD and efficacy studies
In vivo efficacy panel screens (indication or target focused)
In licensing of models for internal studies
Custom model development
Orthotopic and radiotherapy studies
Ex vivo and organoid studies

We are hiring a dynamic and results-driven Director of Business Development to join our team at XenoSTART. As a key player in our sales force, you will be responsible for understanding XenoSTART's unique selling proposition and translating it into effective solutions tailored to each customer's needs. This role requires a keen understanding of the Pre-Clinical sales process along with the ability to manage and exceed performance objectives in an assigned territory or named accounts. 
This is a remote role. The annual base salary for this role is $140,00 - $150,000 + Commission. However, base pay may vary depending on multiple individualized factors including market location, job-related knowledge, skills, and experience. 

Essential Responsibilities

Meet and or exceed assigned sales and revenue targets.
Expand our share of studies at existing clients.
Acquire new clients in partnership with the demand generation team.
Build client commitment at each stage of the sales process.
Participate in the contract review process to get client consensus, as needed.
Develop and manage comprehensive account development plans (Miller Heiman preferred); track progress against key account development milestones; report progress in regularly scheduled account review sessions.
Identify and build relationships with key decision makers internally and externally.
Manage and record all client interaction through Hubspot. This includes accurate entry and upkeep of details for Accounts, Contacts, Calls, Tasks, Events, Opportunities and Client Referrals for a comprehensive CRM profile of each client.
Work collaboratively with Finance to provide and maintain a regular forecast to ensure the business has clear visibility of future opportunities.
Other duties may be assigned at any time.

Education & Experience


5+ years of sales experience within a CRO, with demonstrated success selling PDX models and/or leveraging a strong scientific background in oncology.

Bachelor&rsquo;s degree required.
Exhibit a high degree of interpersonal and persuasive communication skills.
Demonstrated success in building collaborative relationships within an organization.
Demonstrated success with goal attainment in dynamic environment. 
Demonstrated knowledge of competition and developed persuasive strategies to win competitive opportunities.
Strong analytical skills and the ability to draw conclusions and observations from Market trends.
Strong presentation skills.
Focused, with demonstrated work ethic, personal motivation, and enthusiasm; takes personal pride in accomplishment.

Preferred Education and Experience:

Bachelor&rsquo;s degree in the Sciences.
Prior work experience supporting and working for a company with a focus on Pre-Clinical Oncology studies or Contract Research Organization (CRO), strongly preferred. 

Physical and Travel Requirements:  

Travel Expectations: Travel up to 40%.
Travel and meet clients as necessary, including Europe when necessary.
Travel to clients and trade shows, workshops, etc. as necessary.
Mobility: traveling often involves moving between different locations. Must be able to handle demands of navigating airports, public transportation, and various work environments.
Sitting: Ability to remain seated for extended periods of time.

Best-in-Class Benefits and Perks
We value our employees&rsquo; time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:

Comprehensive health coverage: Medical, dental, and vision insurance provided
Robust retirement planning: 401(k) plan available with employer matching
Financial security: Life and disability insurance for added protection
Flexible financial options: Health savings and flexible spending accounts offered
Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided
Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.


More about The START Center for Cancer Research
Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including for 43 therapies that were approved by the FDA. START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. Learn more at STARTresearch.com.

Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.]]></description>
      <pubDate>Mon, 23 Jun 2025 00:00:00 EDT</pubDate>
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