Scientific Director, Medical Affairs, Gastroenterology IBD Portfolio job opportunity at AbbVie.

Home Jobs In United States Of America Tag: Medical Affairs, Gastroenterology IBD Portfolio Scientific Director, Medical Affairs, Gastroenterology IBD Portfolio position at AbbVie


Date2026-05-01T00:16:02.889Z bot
AbbVie Scientific Director, Medical Affairs, Gastroenterology IBD Portfolio
Experience: General
Pattern: Full-time
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Medical Affairs, Gastroenterology IBD Portfolio

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degreeGeneral
loacation Mettawa, Illinois, United States Of America
loacation Mettawa, Illin..........United States Of America
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Job DescriptionThe Scientific Director provides medical and scientific strategic and operational input into core medical affairs activities such as: health-care professional and provider interactions (Payers, Patients, Prescribers, and Providers); generation of clinical and scientific data (enhancing therapeutic benefit and value); educational initiatives (medical education, data, guidelines, and value proposition); safeguarding patient safety (risk minimization activities and safety surveillance activities).The Scientific Director works closely with commercial teams to provide strategic medical input into core brand (product) strategies, and to support medical and marketing activities (promotional material generation and product launches) and market access;  Collaborates with clinical development on Medical Affairs support of priority trials.        Responsibilities:With oversight, contributes to the development of brand strategies. Actively contributes to the development of a TA EE Engagement Plan.Leads and support Medical Affairs initiatives for the target indication.Develops and executes Medical Affairs support of priority clinical development trials.Contributes to the development of and leads the execution of the Medical Education / Advisory Board & EE Engagement Plan generation in line with TA plan. Lead the individual (Global) Conference planning and execution.Generates clinical and scientific data per evidence gap assessment.Responsible to manage budget for assigned projects.Aligns Medical education and scientific initiatives with Sci Comm Platform. Informs Investigator Initiated Study (IIS) strategy and can act as Docent for IISs.Contributes to the generation of MI communication content and supports training on Medical Information (MI) materials.Participates in design and execution of clinical trial safety, product safety and risk management plans. Track RMP implementation.Responsible for performing the accurate and detailed medical review of complex advertising and promotional materials for assigned therapeutic area(s) within Medical Affairs. Provides timely and accurate reviews of promotional materials in accordance with established policies and practice standards, including regulatory guidelines to meet customer needs.This a hybrid position based out of Lake County, IL .

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