Clinical Development Medical Director, Breast Oncology

Role: Clinical Development Medical Director supporting prifetrastat program, leading clinical trial activities and subteams. Responsibilities: conduct medical monitoring (eligibility, data review, safety), serve as investigator liaison, manage clinical and regulatory docs, provide strategic insights, interpret clinical data, and represent the company externally. Requirements: MD/DO/MBBS/MBChB, 4+ years in clinical research within biopharma, licensed for independent prescribing for at least 2 years. Preferred: Board-certified/eligible in oncology, with breast oncology experience and late-phase clinical development background. HighValue: oncology (breast cancer), late-phase trials, regulatory interactions, clinical monitoring, and cross-functional collaboration. WorkSetup: hybrid (live within commuting distance, on-site ~2.5 days/week); travel for conferences as needed.