Leads medical input into disease area strategy and asset strategies within the lung cancer oncology pipeline portfolio.
Leads 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.
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.
Typically, 10-15 years of experience in the pharmaceutical industry or equivalent
7-10 years of experience in Medical Affairs with Global Medical Affairs experience highly preferred.
Substantial knowledge of relevant therapeutic area required.
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.
Senior 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.
Minimum of 2 years of clinical trial or medical affairs experience in the pharmaceutical industry or academia or equivalent. 3+ years of experience is preferred.
Substantial knowledge of relevant therapeutic area required.
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 intera
Benefits
Health insurance
Additional Information
The Medical Affairs 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.
The Scientific Director / Senior Medical Director, Medical Affairs - Global Oncology Pipeline provides medical and scientific input into core strategic and operational pipeline medical affairs activities for the lung cancer portfolio such as: health-care professional and provider interactions; generation of clinical and scientific data (enhancing therapeutic benefit and value); educational initiatives (medical education, scientific communications, and value proposition) and safeguarding patient safety (risk minimization activities and safety surveillance activities). Works closely with sales, marketing, and commercial teams to provide strategic medical input into core brand (product) strategies, and to support medical affairs, marketing activities (promotional material generation and product launches) and market access.
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.
Abbvie · Florham Park, NJ