About the job
As a Medical Advisor at AbbVie, you will play a crucial role in providing specialized medical and scientific guidance for various countries across Western Europe and Canada. Your expertise will contribute to core medical affairs activities, including engaging with healthcare professionals and providers, generating clinical and scientific data to enhance therapeutic value, implementing educational initiatives, and ensuring patient safety through effective risk management and safety surveillance.
Your collaboration with sales, marketing, and commercial teams will ensure that strategic medical insights inform product strategies and support promotional activities and market access initiatives. Join us in our mission to improve patient outcomes through innovative medicines.
Key Responsibilities:
- Lead and oversee assigned products/projects in collaboration with affiliate and Area Medical teams as well as Marketing, Regulatory Affairs, and Clinical departments.
- Establish and approve scientific methodologies for hypothesis generation, study design, and reporting protocols.
- Participate in the design and execution of clinical trial safety assessments and product safety plans, including routine monitoring and reporting of Adverse Events to regulatory authorities.
- Ensure the scientific integrity of clinical trials, resolve safety issues, and interpret statistical analyses to ensure clinical significance.
- Initiate medical affairs activities, disseminate data, and provide scientific education to investigators and Global Project Team members.
- Understand and comply with regulatory requirements related to clinical studies and global drug development, serving as the scientific interface for regulatory discussions.

