Director, Clinical Sciences, Oncology

Role: Support Clinical Development in Oncology by leading and overseeing Phase 1-3 clinical studies, ensuring data quality for regulatory submissions and internal governance. Responsibilities: contribute to trial design, author and review study documents, oversee study execution, data review, safety management, site activation, and regulatory inspection readiness. Also involved in stakeholder engagement, investigator meetings, and training junior staff. Requirements: PhD, PharmD, or advanced degree with 10+ years of biotech/pharma clinical development experience, especially in oncology; expertise in protocol development, data integrity, and regulatory standards; strong communication and leadership skills. High-Value: oncology (clinical trial phases 1-3), data quality, regulatory compliance, cross-functional collaboration with Discovery, Translational Medicine, Regulatory, Biostatistics, and Medical Affairs. Work setup: based in Cambridge, MA or Princeton, NJ; in-office 70% with up to 15% travel, hybrid model.