Clinical Development Medical Director, Breast Oncology

Role: Clinical Development Medical Director supporting prifetrastat development, leading clinical trial activities and subteams. Responsibilities: oversee medical monitoring, data review, safety assessments; serve as liaison with investigators, ethics committees, regulators; contribute to clinical and regulatory document development; provide strategic guidance on development plans; interpret clinical data and communicate insights; represent the company externally. Requirements: MD, DO, MBBS, or MBChB from a recognized medical school, with 4+ years in biopharma clinical research; licensed for independent prescribing for at least 2 years; leadership experience in supporting clinical trials. Preferred: Board certification or eligibility in oncology, especially breast cancer; late-phase clinical development experience. HighValue: oncology (breast), late-phase trials, regulatory interactions, clinical monitoring, cross-functional leadership. WorkSetup: hybrid role, onsite ~2.5 days/week, with travel to conferences; relocation support may be available.