Clinical Development Medical Director, Breast Oncology

Clinical Development Medical Director (prifetrastat program) Responsibilities Conduct medical monitoring activities including eligibility assessment, data review, and safety monitoring. Lead peer-to-peer interactions with investigators. Serve as point of contact for clinical issues among study teams, investigators, ethics committees, steering committees, and regulatory authorities. Lead and contribute to development/maintenance of clinical trial and regulatory documents with Clinical Scientists and cross-functional teams. Provide clinical development leadership across several study teams. Represent Clinical Development on subteams including for Marketing Authorization Applications. Collaborate with Global Development to create/refine development strategies. Represent the company in external engagements/joint collaborations. Collaborate with Clinical Scientists to review/interpret clinical data, identify key findings, and communicate to stakeholders. Stay current with literature and guidelines to advise and drive current/future clinical development plans. Basic Qualifications Primary medical degree (MD, DO, MBBS, MBChB) from a recognized school. 4+ years biopharmaceutical clinical research & development experience. Licensed to prescribe medicines independently for at least 2 years post intern/house officer/foundation. Preferred Qualifications Board certified/eligible in oncology (or equivalent). Breast oncology experience (2+ years). Late phase clinical development experience. Travel/Location & Benefits Hybrid: live within commuting distance; work onsite ~2.5 days/week. Travel to scientific conferences/meetings several times per year. Relocation support may be available. Eligible for Global Performance Plan bonus (25% target) and share-based long-term incentive; comprehensive benefits including 401(k), paid time off, caregiver/parental and medical leave, and medical/dental/vision. #J-18808-Ljbffr Scorpion Therapeutics