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    <title>AVEO Oncology Jobs</title>
    <link>https://ejob.bz/CompanyPortal.do?companyGK=47514&amp;portalGK=37895</link>
    <description><![CDATA[Job Postings available for application.]]></description>
    <language>en-us</language>
    <pubDate>Sat, 04 Jul 2026 20:00:34 EDT</pubDate>
    <lastBuildDate>Sat, 04 Jul 2026 20:00:34 EDT</lastBuildDate>
    <generator>BrightMove ATS</generator>
    <item>
      <title><![CDATA[Senior Director of Sales Operations and Business Analytics - Boston, MA]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27780562&amp;companyGK=47514&amp;portalGK=37895</link>
      <guid>5b32fa16-5289-4745-85b3-ba1d7d4e3b35</guid>
      <description><![CDATA[JOB TITLE: Senior Director of Sales Operations and Business Analytics 
LOCATION: Boston, MA preferred, remote would be considered for an exceptional candidate                                               
DATE PREPARED: July 2026
 
 AVEO is developing innovative therapies for cancer and is seeking an individual to lead a strong sales operations and business analytics team.  The Senior Director, Sales Operations and Business Analytics, is a key role in the commercial organization responsible for ensuring the optimal infrastructure, support, and insights required by our commercial organization are easily accessible and incorporated into day-to-day reporting and decision making. 
 Reporting to the Chief Commercial Officer, this individual will collaborate with internal and external partners to assess organizational needs and lead our Business Analytics and Sales Operations functions. This role requires strong management experience along with understanding of the oncology marketplace, data analytics and reporting, and project management.  The ideal candidate will have a proven track record of leading teams and executional excellence. 
PRINCIPAL DUTIES:   

Provide hands-on expertise and work collaboratively to design, execute and oversee all commercial analytical deliverables related to our commercial product FOTIVDA and pipeline products, including identifying appropriate data sets and methodologies to conduct analysis plus synthesis & presentation of final output and conclusion. 
Advanced analytics including promotional response and mix modeling, territory opportunity analytics, ROI assessments, and customer assessments. 
Establish data standards, quality controls, and a source-of-truth reporting environment
Work closely with both Commercial, Supply Chain, and Finance leadership to build, analyze, and communicate accurate short-term and long-range demand and revenue forecasts. 
As part of the yearly budget process, define a comprehensive plan and budget integrating all available and to anticipate brand and market challenges. 
Effectively collaborate across AVEO to ensure organizational commitment and alignment with key functions (such as: Marketing, Market Access, and Sales) that are critical to the successful attainment of financial sales goals. 
Display a high degree of creativity and innovation in problem-solving, proactively developing new approaches, processes, and methodologies to maintain consistent and reliable commercial operations. 

&middot;        Manage and develop high performing team- coaching and retaining talent, fostering professional growth, and collaborative culture
&middot;        Lead and empower team through clear goal setting, regular feedback, performance management, and professional development
&middot;        Drive organizational effectiveness by aligning team structure, capabilities, and resources with business priorities while promoting cross-functional collaboration, and continuous improvement.
&middot;       Drive initiatives that leverage AI, machine learning, and automation to enhance decision-making, optimize operations, and deliver actionable insights. 
&middot;       Ensure that these initiatives translate into tangible value for AVEO, enhancing capabilities to advance our commercial solutions. 
&middot;       Partner with IT and commercial leadership to ensure the integrity of the Commercial Data Warehouse and continuously review and integrate various internal and external data sources, ensuring data quality, analytics, and reporting capabilities
&middot;       Oversee the management of other field support such as vehicle program support and materials fulfillment
&middot;       Lead the development and administration of motivational incentive plans and contests designed to support sales and marketing objectives
&middot;       Collaborate with Marketing to ensure customer segmentation and targeting efforts are optimized to increase sales efficiency and impact
&middot;       Develop performance tracking and analytics capabilities including standard performance dashboards and ad hoc support for Marketing, Sales and senior management.  Perform various self-initiated analyses to uncover opportunities and challenges facing the commercialization efforts
REQUIRED QUALIFICATIONS/EXPERIENCE (BASIC QUALIFICATIONS):

Strong analytical abilities and attention to detail with a BA/BS in degree and at least 12 years of experience in the pharmaceutical or biotech industries including launch and pre-launch planning including prior management level experience in Sales Operations.  Minimum of 5 years of oncology market experience.
Extensive experience with IQVIA, KOMODA, SHS and other oncology sales and claims datasets
Advanced computer skills &ndash; excellent knowledge and experience with Microsoft Excel, Word, PowerPoint, Access and Smartsheets
Experience supporting pharmaceutical sales force automation software (Veeva / Salesforce.com preferred)
Ability to translate end user needs into system capabilities
Territory Alignment experience
Sales incentive planning and administration expertise
Ability to work collaboratively as part of a team, and able to manage the needs of multiple stakeholders.
High degree of adaptability and problem-solving skills, with ability to identify and address insight gaps.
Strong written and verbal communication skills, ability to present research results in a clear and concise manner to all levels of the organization.

  About AVEO
 AVEO is a commercial-stage, oncology-focused biopharmaceutical company committed to delivering medicines that provide a better life for patients with cancer. AVEO currently markets FOTIVDA&reg; (tivozanib) in the U.S. for the treatment of adult patients with relapsed or refractory renal cell carcinoma (RCC) following two or more prior systemic therapies. AVEO continues to develop FOTIVDA in immuno-oncology combinations in RCC and other indications and has several other investigational programs in clinical development. AVEO is committed to creating an environment of diversity, equity and inclusion to diversify representation within the Company.
 All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.]]></description>
      <pubDate>Thu, 02 Jul 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Oncology Account Manager - Louisiana, LA]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27779674&amp;companyGK=47514&amp;portalGK=37895</link>
      <guid>cb280ce6-38d5-4704-9dff-6a04b20e30f0</guid>
      <description><![CDATA[JOB TITLE: Oncology Account Manager 
LOCATION: Louisiana (New Orleans, Baton Rouge, Shreveport, Jackson and Gulfport)
DATE PREPARED: June 17, 2026

 

 
JOB SUMMARY:  
 
This position provides a unique opportunity for an experienced sales professional to be part of AVEO&rsquo;s first national sales force to promote FOTIVDA (tivozanib) for renal cell carcinoma (RCC). This role will report to the Regional Business Director and is field based. We are looking for individuals who share the importance of science-based selling, supported by a strong foundation of business analytics. The OAM will also possess a deep knowledge of the oral drug space, as well as background in later line oncology and or hematology malignancy. A solid understanding of the oncology therapeutic area is essential, with a preference for experience in RCC or GU Oncology. Demonstrated sales success and compassion for patients is required.
PRINCIPAL DUTIES:   
 
&middot;       The OAM will promote safe and effective use of FOTIVDA (tivozanib) within the labeled indication (RCC) and in accordance with company training and policies
&middot;       Responsible for individual/territory sales performance and goal attainment
&middot;       Understand the Oncology/RCC environment; have in-depth knowledge of disease-state, local drivers, treatment and referral patterns, etc.
&middot;       Develop strong relationships with key customers practicing in your geography
&middot;       Prepare and implement a comprehensive business plan for territory
&middot;       Exercise sound judgment and ensure integrity and compliance with company policies in all activities and communications
&middot;       Foster AVEO core values and behaviors
REQUIRED QUALIFICATIONS/EXPERIENCE (BASIC QUALIFICATIONS):
 
&middot;       BS in Business or Science; 5 - 10 years sales experience in pharmaceutical/biotechnology industry
&middot;       Demonstrated understanding of oncology therapeutic area, products and marketplace strongly preferred
&middot;       Proven track record that demonstrates top sales accomplishments
&middot;       Demonstrated ability to understand and communicate technical clinical material clearly and effectively
&middot;       Ability to develop critical relationships with physicians, nurses and ancillary staff within academic hospitals, clinics, and private practice facilities
&middot;       Possesses a strong work ethic, ability to develop priorities and manage time appropriately.
&middot;       Works with all members of a team effectively
&middot;       Integrates innovative ideas in order to accomplish corporate and individual objectives
&middot;       Ability to travel and valid driver&rsquo;s license in good standing required
About AVEO
 
AVEO is a commercial-stage, oncology-focused biopharmaceutical company committed to delivering medicines that provide a better life for patients with cancer. AVEO currently markets FOTIVDA&reg; (tivozanib) in the U.S. for the treatment of adult patients with relapsed or refractory renal cell carcinoma (RCC) following two or more prior systemic therapies. AVEO continues to develop FOTIVDA in immuno-oncology combinations in RCC and other indications, and has several other investigational programs in clinical development. AVEO is committed to creating an environment of diversity, equity and inclusion to diversify representation within the Company.
 
 
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.]]></description>
      <pubDate>Thu, 18 Jun 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[SR/Medical Science Liaison - Boston,]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27779472&amp;companyGK=47514&amp;portalGK=37895</link>
      <guid>c35b3170-fca2-4d30-9d33-605896c3c092</guid>
      <description><![CDATA[Title: SR/Medical Science Liaison (MSL)           
Reports To: VP, Head of Medical Affairs
Department: Medical Affairs
Location: Field Based
 
Description: 
The Medical Science Liaison is a trusted partner to key external experts by conducting timely, compliant, and frequent scientific exchanges to enhance the understanding of the scientific and medical value of our products. 
 
The incumbent MSL will have demonstrated ability to execute on stakeholder engagement plans to gather data, develop and share medical insights that contribute to the enhancement of AVEO Oncology key medical messages and plans for future research.  Excellent interpersonal communication and presentation skills are critical as is an organized approach to prioritization of responsibilities and deliverables.  A flexible and adaptable work style, an openness to creativity and ability to work in a team environment with our cross-functional partners is also essential.
 
Duties and Responsibilities (include but not limited to):
&middot;       Identifies, builds and maintains solid relationships with relevant oncology KOLs
&middot;       Presents clinical data to appropriate audiences in a compliant manner
&middot;       Performs therapeutic disease state education in oncology with identified physicians and researchers, Pharm Ds, nurse practitioners, nurses and other health care professionals. 
&middot;       Provide ongoing field updates and insights, including competitive intelligence, and synthesize this information into meaningful, actionable imperatives
&middot;       Attends various scientific conferences to collect and report relevant scientific and clinical data
&middot;       Communication of scientific and clinical data through presentations, (adboards and other forums) abstracts and posters
&middot;       Participates in the development and management of oncology clinical trials
&middot;       Identifies and assists in selection of investigators and oncology clinical trial sites
&middot;       Support speakers training to ensure continued scientific support in the field. (after working cross functionally)
&middot;       Responds to unsolicited request for medical information associated with supported products and disease state area.
&middot;       Provide medical support and expertise to cross-functional partners (Marketing, Training, Market Access, Clinical Development) 
&middot;       Participate in the development and execution of Medical Affairs activities, such Advisory Boards, and development of scientific and medical presentation slides
&middot;       Develop and maintain scientific, clinical and therapeutic expertise in relevant disease states; and deliver medical presentations to both internal and external stakeholders 
&middot;       Demonstrate the ability and desire to work collaboratively, respectfully, and creatively with diverse stakeholders, including leadership within the MSL team 
&middot;       Other responsibilities as business required and assigned
&middot;       Ability to travel for business - Estimated travel ~40-60% 
 
 
Education, Skills and Experience:
 
&middot;       Advanced health care degree required (MD or DO, PhD, PharmD, RN), doctoral degree preferred.
&middot;       Minimum of 6+ years of experience as an MSL in oncology (RCC experience highly desirable); product launch experience preferred.
&middot;       A well-established KOL hematology/oncology network is strongly preferred
&middot;       Proven track record of success in establishing and maintaining thought leader relationships, territory planning, and integration with other field roles
&middot;       Experience working with Thought Leader Engagement (TLE) teams
&middot;       Strong understanding of industry and regulatory guidelines pertinent to compliant interactions with external audiences
&middot;       Demonstrated ability to comprehend complex scientific, medical, and relevant business issues and respond with actionable strategies and tactics to effectively produce timely and measurable results
&middot;       Strong interpersonal and communication skills, both oral and written
&middot;       Excellent ability in searching and interpreting medical literature
&middot;       Technical aptitude for virtual meetings and virtual conferences
&middot;       Flexibility to work outside of standard working hours on an as needed basis
 
Final level will be determined based on the selected candidate's experience and qualifications
 
About AVEO
 AVEO is a commercial-stage, oncology-focused biopharmaceutical company committed to delivering medicines that provide a better life for patients with cancer. AVEO currently markets FOTIVDA&reg; (tivozanib) in the U.S. for the treatment of adult patients with relapsed or refractory renal cell carcinoma (RCC) following two or more prior systemic therapies. AVEO continues to develop FOTIVDA in immuno-oncology combinations in RCC and other indications and has several other investigational programs in clinical development. AVEO is committed to creating an environment of diversity, equity and inclusion to diversify representation within the Company. 
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.]]></description>
      <pubDate>Mon, 15 Jun 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Vice President, Marketing - Boston, MA]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27779033&amp;companyGK=47514&amp;portalGK=37895</link>
      <guid>cddefec3-13c1-46e1-b6b7-705c3966466d</guid>
      <description><![CDATA[JOB TITLE: Vice President, Marketing
LOCATION: Boston, MA                                                                                  PREPARED: June 8, 2026

 

 
JOB SUMMARY:  
 
The Vice President (VP) of Marketing will drive commercial strategy and promotion of AVEO&rsquo;s FOTIVDA (tivozanib) and new product planning preparations for other products in development. The incumbent will provide strategic direction and tactical oversight of marketing programs creating a unique and differentiated approach to campaign execution and brand development. Will oversee vendors and external marketing agencies selection and RFP process and will be responsible for approving branding, communications and collateral development. Further responsibilities include ownership of the strategic business plans and brand P&L, identifying and analyzing competitive landscape, researching new target market segments, and assisting with conferences and external expert development activities.
PRINCIPAL DUTIES:   
 
&middot;       Champion and coordinate product commercialization activities across multiple internal groups and external customers and stakeholders for FOTIVDA
&middot;       Provide leadership in the development and execution of a comprehensive launch plan, consumer strategy, brand building strategy including product positioning, marketing messaging and collaterals, sales and health care professional (HCP) education materials
&middot;       Optimize omnichannel promotional strategy for FOTIVDA for HCPs ensuring appropriate messaging to support brand positioning
&middot;       Support New Product Planning initiatives for AVEO&rsquo;s pipeline agents
&middot;       Develop near, medium, and long-term strategies to target key customer segments assuring commercial growth through platform expansion
&middot;       Oversee various aspects of key conferences and educational initiatives, including advisory boards, webinars and virtual meetings, targeted society meetings, key industry conferences, customer meetings, etc.
&middot;       Oversee management of promotional budgets and vendors by marketing team within company policies
&middot;       Assist in the business forecasting process by evaluating product demand, trends, and SWAT. Regularly analyze and report on market data market research to better understand brand performance
&middot;       Collaborate with TLEs and Medical Affairs to gain insights from key external experts (KOLs) and future product users and stakeholders from third party market research and internal stakeholders, to refine marketing strategies and providing voice-of-the-customer and business intelligence to AVEO&rsquo;s management team
&middot;       Monitor competitive intelligence and collaborate across all functions to develop plans to proactively position competitors and inform the marketing strategy
&middot;       Develop reporting procedures for determining effectiveness and ROI of marketing investment, including communication regarding results and presentations to senior leadership
&middot;       Effectively collaborate with Regulatory, Legal/Compliance, Medical Affairs, Market Access, Quality and all other functional areas, as required, to ensure marketing tools are deployed according to policy
&middot;       Lead, manage and mentor marketing department employees and promote a cross-functional, collaborative mindset  
&middot;       Other duties and responsibilities as required
 
REQUIRED QUALIFICATIONS/EXPERIENCE (BASIC QUALIFICATIONS):
 
&middot;       Bachelor&rsquo;s degree (graduate degree preferred)
&middot;       15+ years of marketing leadership experience in the biotech/pharmaceutical industry.  Demonstrated and recent experience in oncology (experience in renal cell carcinoma; GI cancers; oral oncolytics highly preferred) 
&middot;       Track record of successfully launching Oncology and Specialty Disease products in highly competitive categories
&middot;       Strategic thinking: An understanding of sales and marketing priorities that have maximum impact on decision-makers in the provider base responsible for administering and prescribing 
&middot;       Clear understanding of the patient and treatment journeys 
&middot;       Demonstrated success in product launches in Oncology & Specialty Disease
&middot;       Experience and success in developing product positioning, brand identity and treatment experience
&middot;       Novel thinker with a proven track record of developing new marketing and sales opportunities in creative ways.  Willing to challenge the status quo and try things differently
&middot;       Passionate owner of &ldquo;the message&rdquo; &ndash; one who comfortably communicates with people across levels and across different types of organizations and drives to common points of interest. Able to integrate resources to achieve strategic objectives, build and maintain strong relationships with internal and external stakeholders.
&middot;       Exceptional planning and organizational skills with the ability to effectively contribute to broader partnership strategies and track multiple ongoing projects simultaneously.
&middot;       You thrive in a smaller company environment and love the pace of a pre-commercial and early commercial phase biotech
&middot;       Team Player who can readily pivot between being strategically focused and &ldquo;rolling up the sleeves&rdquo; to ensure deliverables are met, frequently within tight time constraints
 
About AVEO
 
AVEO is a commercial-stage, oncology-focused biopharmaceutical company committed to delivering medicines that provide a better life for patients with cancer. AVEO currently markets FOTIVDA&reg; (tivozanib) in the U.S. for the treatment of adult patients with relapsed or refractory renal cell carcinoma (RCC) following two or more prior systemic therapies. AVEO continues to develop FOTIVDA in immuno-oncology combinations in RCC and other indications, and has several other investigational programs in clinical development. AVEO is committed to creating an environment of diversity, equity and inclusion to diversify representation within the Company.
 
 
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.]]></description>
      <pubDate>Mon, 08 Jun 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Oncology Account Manager - Omaha, NE]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27779009&amp;companyGK=47514&amp;portalGK=37895</link>
      <guid>227509e1-80e5-4e3d-b647-98726b34025d</guid>
      <description><![CDATA[JOB TITLE: Oncology Account Manager 
LOCATION: Omaha, NE                                                
DATE PREPARED: June 7, 2026

 

 
JOB SUMMARY:  
 
This position provides a unique opportunity for an experienced sales professional to be part of AVEO&rsquo;s first national sales force to promote FOTIVDA (tivozanib) for renal cell carcinoma (RCC). This role will report to the Regional Business Director and is field based. We are looking for individuals who share the importance of science-based selling, supported by a strong foundation of business analytics. The OAM will also possess a deep knowledge of the oral drug space, as well as background in later line oncology and or hematology malignancy. A solid understanding of the oncology therapeutic area is essential, with a preference for experience in RCC or GU Oncology. Demonstrated sales success and compassion for patients is required.
PRINCIPAL DUTIES:   
 
&middot;       The OAM will promote safe and effective use of FOTIVDA (tivozanib) within the labeled indication (RCC) and in accordance with company training and policies
&middot;       Responsible for individual/territory sales performance and goal attainment
&middot;       Understand the Oncology/RCC environment; have in-depth knowledge of disease-state, local drivers, treatment and referral patterns, etc.
&middot;       Develop strong relationships with key customers practicing in your geography
&middot;       Prepare and implement a comprehensive business plan for territory
&middot;       Exercise sound judgment and ensure integrity and compliance with company policies in all activities and communications
&middot;       Foster AVEO core values and behaviors
REQUIRED QUALIFICATIONS/EXPERIENCE (BASIC QUALIFICATIONS):
 
&middot;       BS in Business or Science; 5 - 10 years sales experience in pharmaceutical/biotechnology industry
&middot;       Demonstrated understanding of oncology therapeutic area, products and marketplace strongly preferred
&middot;       Proven track record that demonstrates top sales accomplishments
&middot;       Demonstrated ability to understand and communicate technical clinical material clearly and effectively
&middot;       Ability to develop critical relationships with physicians, nurses and ancillary staff within academic hospitals, clinics, and private practice facilities
&middot;       Possesses a strong work ethic, ability to develop priorities and manage time appropriately.
&middot;       Works with all members of a team effectively
&middot;       Integrates innovative ideas in order to accomplish corporate and individual objectives
&middot;       Ability to travel and valid driver&rsquo;s license in good standing required
About AVEO
 
AVEO is a commercial-stage, oncology-focused biopharmaceutical company committed to delivering medicines that provide a better life for patients with cancer. AVEO currently markets FOTIVDA&reg; (tivozanib) in the U.S. for the treatment of adult patients with relapsed or refractory renal cell carcinoma (RCC) following two or more prior systemic therapies. AVEO continues to develop FOTIVDA in immuno-oncology combinations in RCC and other indications, and has several other investigational programs in clinical development. AVEO is committed to creating an environment of diversity, equity and inclusion to diversify representation within the Company.
 
 
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.]]></description>
      <pubDate>Sun, 07 Jun 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Executive Director, Regulatory Operations and Submission Management - Boston, MA]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27778825&amp;companyGK=47514&amp;portalGK=37895</link>
      <guid>56a79af1-95b2-457f-93fe-bb08ce180a52</guid>
      <description><![CDATA[JOB TITLE: Executive Director, Regulatory Operations and Submission Management
DEPARTMENT: Regulatory Affairs
REPORTS TO: Head of Regulatory Affairs
SUPERVISES: Director and below, and/or matrixed Regulatory Affairs staff
DATE PREPARED: May 20, 2026

JOB SUMMARY
The Executive Director, Regulatory Operations will provide strategic and operational leadership for global regulatory operations and systems, submission management and execution across the product portfolio and lifecycle. This role is accountable to build and lead a highperforming Regulatory Operations function and for ensuring submission quality, compliance with current regulations, and timeliness across global regions. 
The Executive Director will oversee endtoend submission operations including systems and technology, submission planning, management, and tracking, document readiness and quality control, publishing, dispatch, archival, and submission lifecycle management. The role will be accountable to establish operations process excellence, including SOPs/work instructions/templates/standards, operational metrics, vendor governance, and inspection readiness for regulated systems and regulatory archives. The role will be expected to maintain a current knowledge of the global regulatory environment, implement changes within the AVEO environment to align with global regulatory expectations, and effectively communicate to cross functional stakeholders and executive leaders. 
The Executive Director will serve as the business owner for regulatory systems and information management capabilities (e.g., RIM and publishing platforms), driving optimization, data governance, and scalable ways of working as the organization grows. The position requires deep expertise in global submission standards (eCTD/CTD), strong project/program leadership, and the ability to influence and partner across Regulatory Affairs, Medical Writing, CMC/Technical Operations, Quality, Clinical, and IT in a fastpaced environment.
PRINCIPAL DUTIES
&middot;       Establish and lead the Regulatory Operations strategy and execution to deliver compliant, highquality global submissions and maintain submission/registration archives across the product lifecycle (development through postapproval). 
&middot;       Build, develop, and manage a Regulatory Operations organization (direct reports, vendors and/or matrix resources), including capability building, training, performance management, and succession planning. 
&middot;       Oversee submission planning, tracking, publishing, compilation, QC, dispatch, and archiving for major submission types (e.g., INDs/CTAs, NDAs/BLAs/MAAs, amendments/supplements/variations, annual reports, and other lifecycle submissions), ensuring adherence to global health authority technical requirements and timelines. 
&middot;       Serve as the operational submission execution partner to Regulatory Strategy and Regulatory CMC leads and crossfunctional teams, translating regulatory milestones into feasible operational plans, resourcing models, and publishing schedules while proactively identifying risks and mitigation strategies. 
&middot;       Establish and lead Regulatory Operations process excellence, including creating/maintaining SOPs, work instructions, templates, style guides, and best practices for document readiness, publishing, archival, and controlled submission records. 
&middot;       Establish and manage quality systems for Regulatory Operations, including technical QC standards (formatting, hyperlinks/bookmarks, PDF requirements, metadata), submission readiness checks, error prevention, corrective actions, and continuous improvement initiatives. 
&middot;       Lead Regulatory Information Management (RIM) and publishing systems governance, acting as business owner for tools supporting submission planning/content management/publishing/archival and regulatory data integrity; partner with IT and Quality on validation, access controls, audit trails, change control, and vendor-managed services where applicable. 
&middot;       Oversee and manage external vendors/outsourcing partners (publishing, system providers, ancillary submission services) including scope definition, budgets, performance monitoring, and issue resolution. 
&middot;       Ensure inspection readiness for Regulatory Operations processes, regulated systems, and submission archives; support audits/inspections by preparing evidence packages, demonstrating system/process controls, and coordinating responses and CAPAs in partnership with Quality. 
&middot;       Maintain regulatory operations intelligence regarding evolving global electronic submission standards and operational requirements (e.g., agency technical specifications, lifecycle management expectations), and lead change implementation to keep the organization compliant and current. 
&middot;       Partner cross-functionally with Regulatory Affairs Strategy, Medical Writing, CMC/Technical Operations, Quality, Biometrics, Clinical Operations, IT and Project Management to embed operational excellence and predictable submission execution into integrated development plans.
REQUIRED QUALIFICATIONS / EXPERIENCE
Education
Bachelor&rsquo;s degree in Life Sciences or related discipline required. 
 
Experience

15+ years of progressive experience in Regulatory Operations and global submission management/publishing within pharmaceutical and/or biotechnology organizations, including leadership responsibility. 
Demonstrated experience leading endtoend submission execution (planning, publishing, QC, dispatch, archival) for U.S. and exU.S. submissions, with strong knowledge of global submission formats and technical standards (eCTD/CTD/ACTD, as applicable). 
Proven experience serving as business owner and implementing/optimizing regulatory systems (e.g., RIM/publishing/content management), including data governance and user adoption. 
Experience establishing SOPs/standards and driving operational and quality process improvements in a regulated environment. 
Experience managing vendors/outsourcing partners and developing scalable operating models (insourcing/outsourcing mix) across different stages of company growth. 

Skills

In-depth, working, knowledge and understanding of FDA, EMA and ICH regulations and guidelines governing electronic submission standards.
Expert knowledge of electronic submission publishing concepts and technical QC expectations (e.g., document formatting standards, hyperlinking/bookmarking, PDF technical requirements, metadata integrity). 
Strong ability to lead and influence crossfunctional, matrixed teams, excellent stakeholder management and strong executive communication skills.
Comfortable with a player/coach role with an enterprise mindset.

DISCLAIMER
This job description is intended to describe the general nature and level of work being performed by employees assigned to this position. It is not intended to be an exhaustive list of all responsibilities, duties, or skills. The Company reserves the right to modify duties and responsibilities as business needs evolve]]></description>
      <pubDate>Thu, 04 Jun 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Controller - Boston, MA]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27778759&amp;companyGK=47514&amp;portalGK=37895</link>
      <guid>99e53461-479b-41c0-b81c-660ca20f5fad</guid>
      <description><![CDATA[JOB TITLE: Controller
DEPARTMENT: Finance 
REPORTS TO: CFO 
LOCATION: Boston, MA/ On-Site a minimum of 3 times a Week DATE   
PREPARED: June 4, 2026

 

 
JOB SUMMARY:  
 
AVEO Oncology, located in the Seaport district of Boston is looking for a controller to join the Finance team.  This position will be a key Finance business partner supporting Finance, Operations and Commercial Functions. The Controller must be detail oriented, organized, able to prioritize tasks to meet deadlines and flexible to manage multiple initiatives in a fast-paced environment. The ideal candidate must possess a &ldquo;can do&rdquo; attitude and willingness to roll up his / her sleeves.
PRINCIPAL DUTIES:   
 
&middot;       Operate the day to day accounting, partnering with business units and cultivating relationships that drive the business forward.
&middot;       the general accounting operations, ensuring compliance with GAAP, and the preparation of accurate and timely financial statements and management reports.
&middot;       Oversee monthly, quarterly and annual closing processes 
&middot;       Ensure compliance with statutory reporting, tax filings, internal and external audits and act as the primary liaison between the company and all regulatory agencies and external audit teams.
&middot;       Manage company cash flow, optimization of company capital.
&middot;       Develop and implement internal controls to safeguard company assets and ensure accurate financial reporting.
&middot;       Oversee risk management and compliance initiatives, ensuring adherence to legal and financial regulations.
&middot;       Conduct monthly, quarterly and yearly analyses to assess financial performance.
&middot;       Monitor project budgets
&middot;       Partner with cross functional teams(R&D, Commercials, HR, and Leadership) to drive data transformation and accelerate decision-making through clearer financial insights
&middot;       Key contributor to strategic long range planning.
&middot;       Liaison with parent company partners in Korea
&middot;       Establish best practices in accounting operations by establishing a culture of continuous improvement.
&middot;       Mentor the accounting team, fostering a culture of high performance and accountability.
&middot;       Build and develop a high-performing accounting function capable of supporting he company&rsquo;s growth objectives.
 
REQUIRED QUALIFICATIONS/EXPERIENCE (BASIC QUALIFICATIONS):
 
&middot;       Bachelor&rsquo;s degree in Accounting or Finance required
&middot;       CPA required
&middot;       Fluent in Korean and English required
&middot;       Experience with Commercial stage BioPharma accounting preferred
&middot;       Experience with SAP, Gross to Net accounting, manufacturing practices
&middot;       15+ years of accounting experience with experience in the life sciences industry preferred
&middot;       Proven experience with Business partnering and effectively building relationships with the ability to influence and challenge in a positive way
&middot;       Experience in supporting external audits and quarterly reviews, and SOX compliance testing required
&middot;       Strong proficiency in Excel and Smart sheets
&middot;       Strong organizational skills with the ability to prioritize tasks to meet deadlines
&middot;       Must be detail oriented and ensure the accuracy and completeness in all work product deliverables.
&middot;       Ability to manage multiple initiatives in a fast-paced environment 
&middot;       Possess a &ldquo;can do&rdquo; attitude and willingness to roll-up sleeves
&middot;       Strong communication skills with an internal and external customer focus
&middot;       Continuous mindset for process and efficiency improvements
 
About AVEO
 
AVEO is a commercial-stage, oncology-focused biopharmaceutical company committed to delivering medicines that provide a better life for patients with cancer. AVEO currently markets FOTIVDA&reg; (tivozanib) in the U.S. for the treatment of adult patients with relapsed or refractory renal cell carcinoma (RCC) following two or more prior systemic therapies. AVEO continues to develop FOTIVDA in immuno-oncology combinations in RCC and other indications, and has several other investigational programs in clinical development. AVEO is committed to creating an environment of diversity, equity and inclusion to diversify representation within the Company.
 
 
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.]]></description>
      <pubDate>Wed, 03 Jun 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Senior Manager, Investigational Supply Operations - Boston, MA]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27778447&amp;companyGK=47514&amp;portalGK=37895</link>
      <guid>cba0164c-04ea-4f1a-8aca-91a3e1f12631</guid>
      <description><![CDATA[JOB TITLE:                                                  Senior Manager, Investigational Supply Operations     
 DEPARTMENT:                                          Technical Operations / CMC           
 REPORTS TO:                                            Associate Director, Investigational Supply Operations 
 LOCATION:                                                 Remote
DATE PREPARED:                                      June 1, 2026

 

 
JOB SUMMARY:
 
The Senior Manager, Investigational Supply Operations, is responsible for coordination of investigational medicinal product (IMP) supply planning, labeling, packaging, distribution, inventory monitoring, and reconciliation for assigned clinical studies.
 
PRINCIPAL DUTIES:    
 

Proactive planning for clinical supply including secondary packaging, labeling, storage, and distribution.
Proposes packaging and labeling resupply schedules based on forecasts and production lead times. 
Develops strategies for proactively monitoring depot inventory levels and initiating resupplies or transfers to avoid supply interruptions to study sites.
Manages external resources and vendors to accomplish defined clinical supply plans as necessary.
Develop and maintain functional SOPs and controlled documents to ensure compliance to GMP/GCP. 

&middot;       Manage and tracks drug product shipments to clinical depots and sites.
&middot;       Receive, triage, and resolve IMP temperature excursions.
&middot;       Maintain inventory levels of packaging and distribution components.
&middot;       Manage study closeouts and perform study-level reconciliation of IMP.

Function as clinical supply point person on cross functional projects to identify and escalate supply risks.
Provides input to IRT specification design. Reviews assigned IRT threshold levels to optimizes use of clinical supplies and prevent stock outs. 
Collaborate with Clinical Operations to develop and maintain Pharmacy Manuals for Clinical Trials. 

 
REQUIRED QUALIFICATIONS/EXPERIENCE (BASIC QUALIFICATIONS):
 
&middot;       Ability to work well with changing priorities, strong attention to detail.
&middot;       Ability to strategically plan, organize and manage multiple projects simultaneously.
&middot;       Solid vendor management skills.
&middot;       Exceptional project management abilities, particularly within complex clinical programs.
&middot;       Ability to prioritize tasks/issues and identify risks in the future in a proactive manner. 
 
 ADDITIONAL PREFERRED QUALIFICATIONS/EXPERIENCE:
 

Bachelor&rsquo;s degree or higher, preferably in a science discipline, with at least 5 years in a position directly related to successfully managing clinical supplies.  


Thorough understanding of GMP, GCP, and ICH standards governing IMP labeling, packaging, and global distribution. 
Demonstrated experience in managing multiple Phase 1-3 studies, including global clinical supply chains in the pharmaceutical and/or biotech industry.
Understanding of the complete drug supply chain: Drug Substance/Drug Product/Regulatory Submissions and steps required for compliant drug release approvals and Global Importation logistics process.
Proficiency in all aspects of Microsoft applications (Excel, Word, PowerPoint, Project, etc.), experience with automated applications (Excel, Word, PowerPoint, Project, etc.), experience with automated inventory systems, forecasting software and ERP Inventory management is a plus.
Experience with electronic interactive response technologies (IRT) for inventory management. 

 
 
This job description is intended to describe the general nature and level of the work being performed by employees in the position.  It is not intended to be a complete list of all responsibilities, duties, and skills for the position.  The Company reserves the right at all times, in its sole discretion, to add or subtract duties and responsibilities, as it deems necessary.]]></description>
      <pubDate>Fri, 29 May 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Executive Director, Regulatory Affairs - Boston, MA]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27774419&amp;companyGK=47514&amp;portalGK=37895</link>
      <guid>d2a327fc-e2ae-482e-a031-4067560382fc</guid>
      <description><![CDATA[JOB TITLE: Executive Director, Global Regulatory Affairs
DEPARTMENT: Regulatory Affairs
REPORTS TO: Vice President, Regulatory Affairs / Sr. Vice President, Regulatory Affairs
LOCATION: Boston, MA                                                                   
DATE PREPARED: March 27, 2026

 

 
JOB SUMMARY:  
The Executive Director, Global Regulatory Affairs will provide strategic and operational leadership for global regulatory activities across the company&rsquo;s oncology portfolio and will be accountable for the development and execution of integrated global regulatory strategies across the full product lifecycle, from early clinical development through registration, commercialization, and postapproval lifecycle management.
Serving as a senior member of the Regulatory Affairs leadership team, this role will oversee multiple oncology programs and/or therapeutic areas and will act as a key regulatory advisor to executive leadership and crossfunctional governance bodies. The Executive Director will ensure that regulatory strategies are aligned with corporate objectives, development priorities, and commercial goals, while enabling efficient and compliant pathways to approval in major global markets.
This position requires deep regulatory expertise in oncology drug and biologic development, strong leadership and decisionmaking capabilities, and the ability to influence at the enterprise level. The Executive Director will lead global Health Authority engagement strategies, drive regulatory excellence across the organization, and build and mentor highperforming regulatory teams in a dynamic oncology biotech environment.
PRINCIPAL DUTIES:   

Provide executivelevel regulatory leadership and oversight for assigned oncology programs and/or portfolio segments, ensuring the development and execution of robust global regulatory strategies across the full product lifecycle, from early clinical development through registration, commercialization, and postapproval activities.
Serve as, or oversee, Global Regulatory Leaders (GRLs) for oncology programs, ensuring consistent, highquality regulatory strategy development and execution across programs, indications, and regions.
Accountable for regulatory strategy input into corporate, portfolio, and development governance, including assessment of regulatory risk, probability of success, and mitigation strategies to support informed decisionmaking by senior leadership.
Lead and oversee global Health Authority engagement strategies, including FDA, EMA, and other international regulatory agencies, and provide executive oversight for major regulatory interactions (e.g., preIND, EndofPhase, scientific advice, preBLA/MAA).
Ensure the preparation, review, and approval of highquality regulatory submissions and related documentation, including but not limited to INDs/CTAs, scientific advice packages, orphan drug applications, PIPs/PSPs, BLAs/MAAs, labeling strategy and negotiations, responses to regulatory questions, and postapproval commitments.
Provide strategic oversight for regulatory approaches involving companion diagnostics (CDx), biomarkers, devices, and combination products, ensuring alignment of therapeutic and diagnostic development strategies.
Drive the evaluation and application of special regulatory pathways and expedited programs (e.g., orphan drug designation, breakthrough therapy designation, Fast Track, accelerated approval, PRIME, compassionate use, pediatric plans, diversity action plans), ensuring alignment with program and portfolio objectives.
Maintain a high level of regulatory intelligence and competitive awareness, monitoring evolving regulatory requirements, precedents, and external trends, and proactively adapting regulatory strategies to maintain competitive advantage.
Partner closely with Clinical Development, Clinical Operations, CMC/Technical Operations, Nonclinical, Biometrics, Medical Affairs, Commercial, and Project Management to ensure regulatory considerations are fully integrated into development and commercialization plans.
Represent Regulatory Affairs as a senior leader within crossfunctional teams, Global Product Teams, and internal governance forums, and serve as a key regulatory spokesperson for the company as appropriate.
Build, lead, and develop a highperforming Regulatory Affairs organization by setting clear expectations, providing mentorship and career development, and fostering a culture of accountability, collaboration, and regulatory excellence.
Ensure compliance with global regulatory requirements and internal policies, and support continuous improvement of regulatory processes, systems, and capabilities to support organizational growth.

REQUIRED QUALIFICATIONS/EXPERIENCE (BASIC QUALIFICATIONS):
 Education

Bachelor&rsquo;s degree in Life Sciences or a related discipline required; advanced scientific degree (MS, PhD, PharmD, MD, or equivalent) strongly preferred.

Experience

15+ years of progressive Regulatory Affairs experience within the pharmaceutical and/or biotechnology  industry (small molecule and/or well characterized biologics).
Demonstrated success leading global regulatory strategies for multiple development programs across clinical stages (Phase 1&ndash;4), including experience with global registrations.
Proven experience interacting with global Health Authorities (e.g., FDA, EMA) at a senior level.
Experience negotiating patient reported outcomes and other clinical outcomes assessments with FDA and/or EMA.
Experience in oncology and/or rare diseases is required. 
Demonstrated experience managing and developing senior regulatory leaders and teams as a player/coach in a matrixed, crossfunctional environment.

Skills

Demonstrated deep knowledge of global regulatory requirements governing oncology drug and biologic development.
Demonstrated strong strategic thinking, risk assessment, and decisionmaking capabilities.
Ability to influence and collaborate effectively with executive leadership and crossfunctional stakeholders.
Excellent written and verbal communication skills, including the ability to communicate complex regulatory issues to executive leadership.
Experience with electronic submission processes and global regulatory information management systems.

 
 About AVEO
 
AVEO is a commercial-stage, oncology-focused biopharmaceutical company committed to delivering medicines that provide a better life for patients with cancer. AVEO currently markets FOTIVDA&reg; (tivozanib) in the U.S. for the treatment of adult patients with relapsed or refractory renal cell carcinoma (RCC) following two or more prior systemic therapies. AVEO continues to develop FOTIVDA in immuno-oncology combinations in RCC and other indications, and has several other investigational programs in clinical development. AVEO is committed to creating an environment of diversity, equity and inclusion to diversify representation within the Company.
 
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.]]></description>
      <pubDate>Fri, 27 Mar 2026 00:00:00 EDT</pubDate>
    </item>
    <item>
      <title><![CDATA[Medical Director - Boston, MA]]></title>
      <link>https://ejob.bz/jb.do?reqGK=27773779&amp;companyGK=47514&amp;portalGK=37895</link>
      <guid>01d28b4b-c8f5-48fa-a800-e024c570575e</guid>
      <description><![CDATA[JOB TITLE: Medical Director, Oncology  
Dept:  Clinical Development                      
REPORTS TO: Senior Vice President, Head of Clinical Development
Location: Boston, MA
DATE PREPARED: March 12, 2026 

 

 
JOB SUMMARY:  
AVEO Oncology is seeking a highly skilled and experienced Medical Director to join our dynamic team. The successful candidate will have a strong background in oncology, specifically renal cancer, previous experience in early phase development strongly preferred; and a proven track record in managing global clinical trials. This role is pivotal in driving the clinical development of our oncology pipeline and ensuring the successful execution of our clinical programs.
 
PRINCIPAL DUTIES:   
1.      Leadership skills:
&middot;       Provide medical and scientific leadership in the design, execution, and interpretation of Phase I clinical studies.
&middot;       Collaborate with cross-functional teams, including clinical operations, regulatory affairs, and biostatistics, to ensure alignment on clinical strategy and study design.
&middot;       Ensure clinical trials are conducted in compliance with applicable regulations, guidelines, and company policies.
&middot;       Oversee clinical aspects of global clinical studies, ensuring consistency and quality across all regions.
&middot;       Lead interactions with key opinion leaders to align clinical development plans.
2.      Medical Monitoring and Safety Oversight:
&middot;       Serve as the medical monitor for assigned clinical trials, providing ongoing medical oversight and guidance, addressing any issues that arise to ensure timely completion and high-quality data.
&middot;       Assess and interpret clinical trial data, ensuring accuracy and completeness of safety and efficacy information.
&middot;       Collaborate with pharmacovigilance teams to monitor and manage adverse events and other safety concerns.
3.      Data Analysis and Reporting:
&middot;       Participate in data analysis, interpretation, and presentation of clinical study results to internal and external stakeholders.
&middot;       Contribute to the preparation of clinical study reports, regulatory submissions, and scientific publications.
&middot;       Present clinical data at scientific conferences and advisory boards.
4.      Stakeholder Engagement:
&middot;       Develop and maintain strong relationships with key opinion leaders, investigators, and clinical trial sites.
&middot;       Represent AVEO Oncology at scientific meetings, conferences, and industry events.
REQUIRED QUALIFICATIONS/EXPERIENCE (BASIC QUALIFICATIONS):
Education: 
&middot;       Medical Doctor (MD) degree is required.
Experience:

Minimum of 3-5 years of experience in oncology clinical development, familiarity with Phase I and phase II clinical studies is required.

&middot;       Demonstrated experience in managing global clinical trials and navigating international regulatory environments.
Skills:
&middot;       Strong clinical and scientific acumen in oncology.
&middot;       Excellent leadership, communication, and interpersonal skills.
&middot;       Proven ability to work effectively in a cross-functional, global team environment.
&middot;       Strong analytical and problem-solving skills with keen attention to detail.
Preferred Qualifications:
&middot;       Experience working within a biotechnology or pharmaceutical company.
&middot;       Demonstrated ability to drive clinical development strategies and make data-driven decisions.
&middot;       Prior experience interacting with global regulatory agencies and key opinion leaders.
&middot;       Experience in renal oncology clinical trials.
About AVEO
 
AVEO is a commercial-stage, oncology-focused biopharmaceutical company committed to delivering medicines that provide a better life for patients with cancer. AVEO currently markets FOTIVDA&reg; (tivozanib) in the U.S. for the treatment of adult patients with relapsed or refractory renal cell carcinoma (RCC) following two or more prior systemic therapies. AVEO continues to develop FOTIVDA in immuno-oncology combinations in RCC and other indications and has several other investigational programs in clinical development. AVEO is committed to creating an environment of diversity, equity and inclusion to diversify representation within the Company.
 
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.]]></description>
      <pubDate>Wed, 18 Mar 2026 00:00:00 EDT</pubDate>
    </item>
  </channel>
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