BioSpace
Head of Solid Tumors, Global Medical Affairs Oncology
BioSpace, Florham Park, New Jersey, us, 07932
Head of Solid Tumors, Global Medical Affairs Oncology
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Head of Solid Tumors, Global Medical Affairs Oncology
role at
BioSpace
5 days ago – Be among the first 25 applicants.
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Company Description AbbVie’s mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several therapeutic areas: immunology, oncology, neuroscience, and eye care, and products and services in our Allergan Aesthetics portfolio.
Job Description The Head of Oncology Solid Tumors Medical Affairs will lead and oversee the global medical affairs strategy, execution, and scientific leadership for the oncology solid tumor portfolio. This role requires expertise in oncology drug development, clinical trials, regulatory interactions, and cross‑functional collaboration.
Responsibilities
Leadership and Strategy:
Lead the development and execution of the global medical affairs strategy for the oncology solid tumor portfolio, including pipeline products and marketed therapies.
Provide strategic direction to the oncology medical affairs team, ensuring alignment with overall business and corporate goals.
Collaborate with senior leadership to define and implement the long‑term vision and strategy for oncology solid tumors within the company.
Scientific Expertise and Communication:
Provide deep scientific leadership in oncology solid tumors, including interpretation and communication of clinical data, emerging scientific trends, and new therapeutic approaches.
Serve as the scientific face of the company in external engagements with key opinion leaders, healthcare professionals, academic institutions, and patient advocacy groups.
Ensure effective dissemination of scientific information through publications, congress presentations, advisory boards, and medical education activities.
Cross‑Functional Collaboration:
Work closely with clinical development leaders to align trial design, execution and data interpretation with medical affairs objectives.
Collaborate with regulatory affairs to support regulatory submissions and interactions with health authorities.
Partner with commercial and market access teams to integrate scientific and clinical perspectives into marketing strategies, product positioning, and market access strategies.
Medical Affairs Operations:
Lead the execution of key medical affairs activities, including evidence generation through medical affairs studies, external scientific engagements, and medical education initiatives.
Oversee the generation of scientific publications, abstracts, and posters to ensure timely dissemination of data.
Ensure compliance of all medical affairs activities with regulatory, legal, and ethical standards.
Team Leadership and Development:
Lead and mentor the oncology solid tumor medical affairs team, fostering a high‑performance culture.
Drive professional development initiatives for team members.
Establish clear performance expectations and provide feedback and coaching.
External Engagement:
Build and maintain strong relationships with KOLs, clinical investigators, and external partners.
Represent the company at scientific conferences, industry events, and forums.
Engage in strategic partnerships and collaborations to enhance the company’s scientific reputation.
Qualifications
M.D. or equivalent advanced degree in a relevant scientific discipline.
15+ years of experience in the pharmaceutical or biotechnology industry, focused on oncology solid tumors.
Demonstrated expertise in clinical development, regulatory requirements, and commercialization of oncology therapies.
Proven leadership in medical affairs with cross‑functional teams.
Strong scientific knowledge of solid tumor biology, clinical trial design, biomarker development, and emerging treatment modalities.
Excellent communication skills for technical and non‑technical audiences.
Preferred Skills
Experience with solid tumor therapies in key areas such as NSCLC, CRC, gynecologic tumors.
Familiarity with advanced modalities such as ADCs, combination therapies, and immuno‑oncology.
Publication and scientific communication track record in oncology.
Experience managing global medical affairs activities across multiple regions.
Physical Requirements
Ability to travel domestically and internationally (up to 25‑30%).
Additional Information
Compensation range is approximate and may vary by location and role specifics.
Benefits include paid time off, medical/dental/vision insurance, and 401(k) eligibility.
This position may be eligible for short‑term incentive programs.
AbbVie is an equal‑opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, and serving our community. Equal Opportunity Employer/Veterans/Disabled.
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Head of Solid Tumors, Global Medical Affairs Oncology
role at
BioSpace
5 days ago – Be among the first 25 applicants.
Get AI-powered advice on this job and more exclusive features.
Company Description AbbVie’s mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several therapeutic areas: immunology, oncology, neuroscience, and eye care, and products and services in our Allergan Aesthetics portfolio.
Job Description The Head of Oncology Solid Tumors Medical Affairs will lead and oversee the global medical affairs strategy, execution, and scientific leadership for the oncology solid tumor portfolio. This role requires expertise in oncology drug development, clinical trials, regulatory interactions, and cross‑functional collaboration.
Responsibilities
Leadership and Strategy:
Lead the development and execution of the global medical affairs strategy for the oncology solid tumor portfolio, including pipeline products and marketed therapies.
Provide strategic direction to the oncology medical affairs team, ensuring alignment with overall business and corporate goals.
Collaborate with senior leadership to define and implement the long‑term vision and strategy for oncology solid tumors within the company.
Scientific Expertise and Communication:
Provide deep scientific leadership in oncology solid tumors, including interpretation and communication of clinical data, emerging scientific trends, and new therapeutic approaches.
Serve as the scientific face of the company in external engagements with key opinion leaders, healthcare professionals, academic institutions, and patient advocacy groups.
Ensure effective dissemination of scientific information through publications, congress presentations, advisory boards, and medical education activities.
Cross‑Functional Collaboration:
Work closely with clinical development leaders to align trial design, execution and data interpretation with medical affairs objectives.
Collaborate with regulatory affairs to support regulatory submissions and interactions with health authorities.
Partner with commercial and market access teams to integrate scientific and clinical perspectives into marketing strategies, product positioning, and market access strategies.
Medical Affairs Operations:
Lead the execution of key medical affairs activities, including evidence generation through medical affairs studies, external scientific engagements, and medical education initiatives.
Oversee the generation of scientific publications, abstracts, and posters to ensure timely dissemination of data.
Ensure compliance of all medical affairs activities with regulatory, legal, and ethical standards.
Team Leadership and Development:
Lead and mentor the oncology solid tumor medical affairs team, fostering a high‑performance culture.
Drive professional development initiatives for team members.
Establish clear performance expectations and provide feedback and coaching.
External Engagement:
Build and maintain strong relationships with KOLs, clinical investigators, and external partners.
Represent the company at scientific conferences, industry events, and forums.
Engage in strategic partnerships and collaborations to enhance the company’s scientific reputation.
Qualifications
M.D. or equivalent advanced degree in a relevant scientific discipline.
15+ years of experience in the pharmaceutical or biotechnology industry, focused on oncology solid tumors.
Demonstrated expertise in clinical development, regulatory requirements, and commercialization of oncology therapies.
Proven leadership in medical affairs with cross‑functional teams.
Strong scientific knowledge of solid tumor biology, clinical trial design, biomarker development, and emerging treatment modalities.
Excellent communication skills for technical and non‑technical audiences.
Preferred Skills
Experience with solid tumor therapies in key areas such as NSCLC, CRC, gynecologic tumors.
Familiarity with advanced modalities such as ADCs, combination therapies, and immuno‑oncology.
Publication and scientific communication track record in oncology.
Experience managing global medical affairs activities across multiple regions.
Physical Requirements
Ability to travel domestically and internationally (up to 25‑30%).
Additional Information
Compensation range is approximate and may vary by location and role specifics.
Benefits include paid time off, medical/dental/vision insurance, and 401(k) eligibility.
This position may be eligible for short‑term incentive programs.
AbbVie is an equal‑opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, and serving our community. Equal Opportunity Employer/Veterans/Disabled.
#J-18808-Ljbffr