Clinical Development Medical Director, Breast Oncology

Role: Clinical Development Medical Director supporting prifetrastat programs, leading clinical trial activities and cross-functional subteams. Responsibilities: oversee medical monitoring, eligibility, safety, and data review; serve as liaison with investigators, ethics committees, and regulators; contribute to clinical and regulatory document development; provide strategic clinical insights; represent company in external collaborations and development strategy discussions. Requirements: MD/DO/MBBS/MBChB with 4+ years industry experience in clinical research; licensed to prescribe medicines for at least 2 years; experience in biopharma clinical trials, ideally in oncology, with late-phase development knowledge preferred. HighValue: oncology (preferably breast oncology), late-phase clinical trials, regulatory interactions, external stakeholder engagement, hybrid work location with travel to scientific meetings. WorkSetup: hybrid role requiring live within commuting distance; travel several times annually.