Medical Director

Role: Experienced Medical Director leading global oncology clinical trials, responsible for medical oversight, data review, and medical input into regulatory documents. Key duties include developing clinical program strategies, authoring and reviewing clinical and regulatory materials, overseeing safety and signal detection, guiding clinical development plans, and engaging with key opinion leaders to integrate the latest medical insights. The role also involves supporting publication strategies, contributing to clinical study reports, and serving as a medical resource across cross-functional teams. Qualifications: MD with at least 3+ years of industry experience in oncology, including support or leadership in Phase 3 trials; expertise in solid tumors preferred. Required skills include team leadership, medical strategy development, and experience with clinical documentation and regulatory interactions. High-Value: Oncology, solid tumors, clinical development, Phase 3, regulatory documentation, cross-functional collaboration. Work setup: Not specified.