Scientific​/Medical Director, Global Hematology Pipeline, Medical Affairs

Scientific/Medical Director, Global Hematology Pipeline, Medical Affairs

Provides specialist medical and scientific input into core strategic and operational medical affairs activities across the hematology pipeline, including disease and asset strategy, scientific differentiation, value propositions, narratives, publication strategy, evidence generation, and health‑care professional and provider interactions. Works closely with asset strategy, clinical development, value and evidence and commercial teams.

The Medical Affairs organization provides patients, healthcare providers and payers with the practical and clinically relevant information and solutions they need to use Abb Vie products safely and effectively throughout the product lifecycle and the patient’s journey.

Position can be based at Mettawa, IL, Florham Park, NJ, or South San Francisco, CA and will follow a hybrid schedule of Tuesdays–Thursdays in office.

• Supports the creation and execution of disease and asset strategies.
• Supports pipeline medical evidence generation strategy and execution including company‑sponsored studies, research collaborations and investigator‑initiated studies.
• Leads creation of early scientific narratives, messaging, and communications activities including congress planning, medical education, publication strategies and plans.
• Provides in‑house medical expertise for the disease area and assets, coordinating appropriate scientific activities with internal and external stakeholders as they relate to ongoing programs; may participate in due diligence or other business development activity as required and contribute to translational strategy in partnership with discovery colleagues.
• Acts as a medical interface and actively solicits insights and opinion through the development and execution of medical expert engagement strategies, partnering with clinical development, commercial, access, area and affiliate colleagues to ensure broad perspectives internally and externally are incorporated into strategies and plans as appropriate.
• Provides scientific/medical education to investigators, clinical monitors and Global Project Team members related to therapeutic area or disease‑specific information; keeps abreast of professional information and technology through conferences and/or medical literature and acts as a therapeutic area resource.
• May assist in the development of medical education programs, advisories and symposia; assists with the scientific review, development, approval, execution and communication of affiliate/area/global medical affairs sponsored or supported clinical research activities.
• May interact with and coordinate appropriate scientific and medical activities with internal stakeholders (e.g., commercial, clinical operations, discovery, statistics, regulatory) as they relate to on‑going medical affairs projects; serves as the scientific team interface for key regulatory discussions.
• Ensures budgets, timelines and compliance requirements are factored into programs’ scientific activities.

• Advanced degree PhD or PharmD; additional post‑doctoral experience highly preferred.
• 5–7+ years of experience in the pharmaceutical industry or equivalent.
• 7–10 years of experience in Medical Affairs with global Medical Affairs experience highly preferred.
• Experience in multiple myeloma and cell therapies highly preferred.
• Knowledge of clinical trial methodology, data analysis and interpretation, regulatory requirements governing clinical trials and experience in development strategy and the design of protocols.
• Proven leadership skills in a cross‑functional global team environment.
• Must possess excellent oral and written English communication skills.

• Medical Doctorate (M.D.) degree or equivalent (D.O. or non‑US equivalent of M.D.); relevant therapeutic specialty in an academic or hospital environment preferred; completion of residency and/or fellowship is preferred.
• 0–2 years of clinical trial or medical affairs experience in the pharmaceutical industry, academia or equivalent; 3+ years of experience preferred.
• Experience in multiple myeloma and cell therapies highly preferred.
• Knowledge of clinical trial methodology, data analysis and interpretation, regulatory requirements governing clinical trials and experience in development strategy and the design of protocols.
• Proven leadership skills in a cross‑functional global team environment.
• Ability to interact externally and internally to support global business strategy.
• Must possess excellent oral and written English communication skills.

Abb Vie 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.

US & Puerto Rico only – to learn more, visit

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