Scientific / Medical Director, Global Hematology Pipeline, Medical Affairs

Responsibilities

• 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.
• 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.
• Ensures budgets, timelines, compliance requirements are factored into programs' scientific activities.
• Scientific Director Qualifications:
• Advanced Degree PhD or PharmD. Additional post doctorate 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 Director Qualifications:
• 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 or academia or equivalent. 3+ years of experience is 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 co

Benefits

Additional Information

The 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 and 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 (MA) organization provides patients, healthcare providers and payers everywhere with the practical and clinically relevant information and solutions they need to use AbbVie products safely and effectively, throughout the product lifecycle and the patient's journey. This position can be based at our Mettawa, IL, Florham Park, NJ, or South San Francisco, CA locations and will follow a hybrid schedule of Tuesdays-Thursdays in office.

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