The SERM Scientific Director provides medical and scientific leadership in the evaluation and management of product safety across clinical development and post‑marketing phases. This role is responsible for assessing benefit‑risk profiles, identifying and managing safety concerns, and supporting regulatory and governance activities to ensure patient safety. The position operates within a global, cross‑functional environment and may include leadership or mentoring responsibilities within a matrix structure.

Responsibilities

• Lead pharmacovigilance and risk management strategy across clinical development and post‑marketing products.
• Evaluate and interpret safety data to inform benefit‑risk assessments and support decision‑making.
• Identify, assess, and elevate safety signals, ensuring appropriate mitigation strategies are implemented.
• Contribute to safety components of regulatory submissions and interactions with regulatory author...