Senior Medical Director, Oncology Clinical Development

Role:
Lead late-stage clinical development in Oncology as Senior Medical Director, focusing on pivotal Phase III trials and registration studies.

• provide medical leadership for trial design, oversight as Medical Monitor, contribute to regulatory submissions, support commercialization, and collaborate cross-functionally with clinical operations, regulatory affairs, pharmacovigilance, biostatistics, and medical affairs
• Serve as external representative and build relationships with investigators, KOLs, and regulators
• Analyze clinical data for efficacy and safety insights, develop lifecycle strategies, and support regulatory interactions

• MD with board certification in Oncology or Hematology-Oncology; 5+ years in clinical development, particularly late-stage oncology trials

• proven track record as Medical Monitor, regulatory submission success, deep understanding of oncology drug development, clinical endpoints, and pathways, with strong leadership and collaboration skills

• oncology, late-stage development, Phase III, clinical trial leadership, medical monitoring, regulatory support, international collaboration, travel up to 30%, based in Cambridge, MA