Director, Regulatory Program Management

Role: Director of Regulatory Program Management leading high-priority regulatory submissions within Summit’s oncology portfolio. Responsibilities: oversee planning and execution of complex global regulatory programs across multiple cancer indications (NSCLC, CRC), partner with cross-functional teams (Regulatory Affairs, Medical Writing, Manufacturing), define milestones, manage risks, and communicate updates to senior leadership. Develop and improve regulatory operating models, support key health authority interactions, and mentor program managers. Requirements: Bachelor's degree with 12+ years of regulatory project management or science experience in pharma, or MS/MBA with 10+ years, or PhD/PharmD/DVM with 6+ years; significant experience in solid tumor oncology, leading complex global regulatory programs, and regulatory submissions. HighValue: oncology, solid tumor, Phase 3, global regulatory leadership, health authority interactions, cross-functional collaboration. WorkSetup: not specified; travel required.