The Medical Director will support clinical trials across early to late development phases, contributing to clinical strategy, safety oversight, and data interpretation. This role involves collaboration across cross‑functional teams to deliver on clinical development goals and regulatory milestones.

This is a Hybrid position.

Key Responsibilities

• Draft and review clinical trial documents (protocols, IBs, ICFs, CSRs).
• Serve as medical monitor for clinical trials, including oversight of external CROs.
• Oversee safety data reporting in coordination with safety and pharmacovigilance teams.
• Support study data interpretation, efficacy/safety analyses, and DSMB activities.
• Contribute to clinical and regulatory strategies and interactions with health authorities.
• Engage with investigators, KOLs, and advisory boards.
• Represent medical input across internal teams and external meetings.