AbbVie
Head of Solid Tumors, Global Medical Affairs Oncology
AbbVie, Florham Park, New Jersey, us, 07932
Head of Solid Tumors, Global Medical Affairs Oncology
AbbVie is seeking a
Head of Solid Tumors, Global Medical Affairs Oncology .
Base pay range $183,000.00/yr – $490,000.00/yr
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 key therapeutic areas—immunology, oncology, neuroscience, and eye care—while also providing a range of products and services in our Allergan Aesthetics portfolio.
Job Description As the Head of Oncology Solid Tumors Medical Affairs, you 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, enabling scientific data to be translated effectively to enhance patient care and meet company goals.
Responsibilities
Leadership and Strategy
Lead the development and execution of the global medical affairs strategy for the oncology solid tumor portfolio.
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 (KOLs), 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 clinical 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 initiatives.
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 all medical affairs activities comply with regulatory, legal, and ethical standards.
Team Leadership and Development
Lead and mentor the oncology solid tumors medical affairs team, fostering a high‑performance culture and ensuring necessary resources, skills, and training.
Drive professional development initiatives to enhance scientific expertise, leadership capabilities, and operational efficiency.
Establish clear performance expectations, conduct evaluations, and provide feedback and coaching.
External Engagement
Build and maintain strong, long‑term relationships with KOLs, clinical investigators, and external partners.
Represent the company at key scientific conferences, industry events, and forums.
Engage in strategic partnerships and collaborations with academic institutions and research organizations.
Qualifications
M.D. or equivalent advanced degree in a relevant scientific discipline (e.g., oncology/hematology).
15+ years of experience in the pharmaceutical or biotechnology industry, focusing on oncology solid tumors.
Demonstrated expertise in clinical development, regulatory requirements, and commercialization of oncology therapies.
Proven leadership experience in medical affairs, managing cross‑functional teams and influencing strategic direction at the senior executive level.
Strong scientific knowledge of solid tumor biology, clinical trial design, biomarker development, and emerging treatment modalities.
Proven ability to lead cross‑functionally and collaborate with clinical development, regulatory, commercial, and other functions.
Exceptional communication skills, with experience presenting complex scientific information to both technical and non‑technical stakeholders.
Preferred Skills
Experience with solid tumor therapies in key areas such as NSCLC, CRC, gynecologic tumors, and others.
Familiarity with advanced cancer treatment modalities such as ADCs, combination therapies, and immuno‑oncology.
Strong publication and scientific communication track record in oncology.
Experience managing global medical affairs activities across multiple geographic regions, focusing on global strategy and the US region.
Physical Requirements
Ability to travel domestically and internationally (up to 25‑30%).
Compensation and Benefits Individual compensation within the posted range will depend on many factors including geographic location.
Comprehensive benefits package: paid time off, medical/dental/vision insurance, 401(k) (eligible employees).
Eligibility to participate in short‑term incentive programs.
Equal Opportunity Statement 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.
Seniority level Executive
Employment type Full‑time
Job function Business Development and Sales
Pharmaceutical Manufacturing and Biotechnology Research
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Head of Solid Tumors, Global Medical Affairs Oncology .
Base pay range $183,000.00/yr – $490,000.00/yr
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 key therapeutic areas—immunology, oncology, neuroscience, and eye care—while also providing a range of products and services in our Allergan Aesthetics portfolio.
Job Description As the Head of Oncology Solid Tumors Medical Affairs, you 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, enabling scientific data to be translated effectively to enhance patient care and meet company goals.
Responsibilities
Leadership and Strategy
Lead the development and execution of the global medical affairs strategy for the oncology solid tumor portfolio.
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 (KOLs), 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 clinical 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 initiatives.
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 all medical affairs activities comply with regulatory, legal, and ethical standards.
Team Leadership and Development
Lead and mentor the oncology solid tumors medical affairs team, fostering a high‑performance culture and ensuring necessary resources, skills, and training.
Drive professional development initiatives to enhance scientific expertise, leadership capabilities, and operational efficiency.
Establish clear performance expectations, conduct evaluations, and provide feedback and coaching.
External Engagement
Build and maintain strong, long‑term relationships with KOLs, clinical investigators, and external partners.
Represent the company at key scientific conferences, industry events, and forums.
Engage in strategic partnerships and collaborations with academic institutions and research organizations.
Qualifications
M.D. or equivalent advanced degree in a relevant scientific discipline (e.g., oncology/hematology).
15+ years of experience in the pharmaceutical or biotechnology industry, focusing on oncology solid tumors.
Demonstrated expertise in clinical development, regulatory requirements, and commercialization of oncology therapies.
Proven leadership experience in medical affairs, managing cross‑functional teams and influencing strategic direction at the senior executive level.
Strong scientific knowledge of solid tumor biology, clinical trial design, biomarker development, and emerging treatment modalities.
Proven ability to lead cross‑functionally and collaborate with clinical development, regulatory, commercial, and other functions.
Exceptional communication skills, with experience presenting complex scientific information to both technical and non‑technical stakeholders.
Preferred Skills
Experience with solid tumor therapies in key areas such as NSCLC, CRC, gynecologic tumors, and others.
Familiarity with advanced cancer treatment modalities such as ADCs, combination therapies, and immuno‑oncology.
Strong publication and scientific communication track record in oncology.
Experience managing global medical affairs activities across multiple geographic regions, focusing on global strategy and the US region.
Physical Requirements
Ability to travel domestically and internationally (up to 25‑30%).
Compensation and Benefits Individual compensation within the posted range will depend on many factors including geographic location.
Comprehensive benefits package: paid time off, medical/dental/vision insurance, 401(k) (eligible employees).
Eligibility to participate in short‑term incentive programs.
Equal Opportunity Statement 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.
Seniority level Executive
Employment type Full‑time
Job function Business Development and Sales
Pharmaceutical Manufacturing and Biotechnology Research
#J-18808-Ljbffr