Home Office: First 3 months full on-site presence for training; afterwards, max. 40%
Your Responsibilities
Own and maintain an expert understanding of the safety profile of assigned product(s)/therapy area(s) and their strategic context (disease, MoA, competitors).
Lead case management and reporting activities: medical review of ICSRs and aggregate reports (e.g., DSUR, PBRER).
Drive signal detection and signal management, including safety assessments and responses to Health Authority requests (incl. quality-related safety topics).
Contribute to and help shape the product safety strategy, including benefit–risk considerations.