Clinical Development Medical Director, Breast Oncology

Role: Clinical Development Medical Director supporting prifetrastat programs, responsible for leading clinical trial activities and cross-functional teams. Responsibilities include medical monitoring (eligibility, safety review), investigator interactions, handling clinical issues, and contributing to development/regulatory documents, while providing strategic insights and clinical data interpretation. Requirements: MD/DO/MBBS/MBChB with 4+ years in biopharma clinical research, licensed to prescribe medicines for at least 2 years post-internship. Preferred: Board certification or eligibility in oncology, breast cancer experience, late-phase clinical development expertise. High-Value: Oncology (likely breast), late-phase trials, regulatory interactions, medical monitoring, and cross-team leadership. Work setup: hybrid role in the US, with travel to scientific meetings as needed.