Clinical Development Medical Director, Breast Oncology

Role: Clinical Development Medical Director for prifetrastat program, leading clinical trial support and subteam management. Responsibilities: oversee medical monitoring, data review, safety, investigator interactions, and clinical issue resolution; develop and maintain clinical and regulatory documents; provide strategic clinical insights; represent the company in external collaborations and regulatory discussions; stay current with clinical developments. Requirements: MD/DO/MBBS/MBChB degree, 4+ years in biopharma R&D, licensed to prescribe medicines for at least 2 years; leadership capabilities, experience in clinical trials supporting development programs, health authority interactions. Preferred: Board certification in oncology, especially breast cancer, late-phase clinical development experience. High-Value: Oncology (breast cancer), late-phase trials, international regulatory engagement, clinical monitoring, cross-functional leadership. WorkSetup: Hybrid role within commuting distance, with travel to scientific meetings; relocation support may be available.