This senior clinical safety leadership role plays a critical part in ensuring patient safety and robust benefit-risk evaluation across global clinical programs in nephrology and metabolic diseases. The position combines hands‑on medical monitoring with strategic pharmacovigilance leadership, ensuring the highest standards of safety oversight from early development through post‑marketing stages. Operating within a fast‑paced, matrixed environment, the role partners closely with clinical development, regulatory, biostatistics, pharmacovigilance, and clinical operations teams. The Senior Director is responsible for guiding safety decision‑making, supporting regulatory interactions, and ensuring consistency in global safety processes. This is a highly influential role where medical judgment directly shapes clinical trial conduct, risk mitigation strategies, and regulatory outcomes.

Accountabilities

• Serve as Medical Monitor for assigned clinical trials (Phase 1...