About the job
Join AbbVie as a Scientific Director in the Global Gynecologic Oncology Pipeline within our esteemed Medical Affairs organization. We are dedicated to providing patients, healthcare providers, and payers with the essential and clinically relevant information needed to utilize AbbVie products safely and effectively throughout the product lifecycle and the patient journey.
In this pivotal role, you will provide specialized medical and scientific strategic and operational insights into key pipeline medical affairs activities, including disease area and asset strategy, evidence generation, early value propositions, narratives, and publication strategy. Collaborating closely with asset strategy, pipeline commercialization, clinical development, and area and affiliate teams, you will play a crucial role in ensuring the successful launch of pipeline assets focused on gynecologic oncology.
This position is primarily based at our Florham Park, NJ location and follows a hybrid work schedule of in-office presence from Tuesday to Thursday. Other AbbVie locations may also be considered under a similar hybrid arrangement.
Key Responsibilities:
- Lead the medical input into disease area and asset strategies within the gynecologic oncology pipeline.
- Oversee the pipeline medical evidence generation strategy and execution, encompassing company-sponsored studies, research collaborations, and investigator-initiated studies.
- Provide in-house medical expertise for disease area and assets, coordinating scientific activities with both internal and external stakeholders related to ongoing programs. Engage in due diligence or business development activities as necessary, and contribute to translational strategies in collaboration with discovery teams.
- Act as a medical liaison, gathering insights and opinions through the execution of medical expert engagement strategies, partnering with clinical development, commercial, access, area, and affiliate teams to ensure comprehensive perspectives are integrated into strategic plans.
- Lead the development of early scientific narratives, messaging, and communication strategies, including congress planning, medical education, and publication strategies.
- Ensure that budgets, timelines, and compliance requirements are effectively managed throughout scientific activities.

