Associate Director, Clinical Operations

Role: Associate Director, Clinical Operations, leading strategic and operational aspects of Corbus's clinical development programs, with a focus on oncology. Responsibilities: develop and oversee clinical development plans; ensure CRO/vendor performance aligns with timelines, quality, and budgets; manage program-level budgets, forecasts, and external spend; review and contribute to clinical documentation including protocols, INDs, and regulatory submissions; support preparation for key regulatory meetings; provide functional leadership and process improvements. Requirements: Bachelor's degree in Life Sciences or related field; 10+ years in pharma/clinical research, including clinical trial/program management across phases 1-4; oncology experience essential; thorough knowledge of FDA and ICH GCP guidelines; expertise managing complex protocols, CROs, budgets, and timelines; experience in global regulatory and compliance standards; strong multitasking, communication, and leadership skills. HighValue: oncology, phase 1-4, global regulatory knowledge, experience managing complex clinical programs, CRO oversight, regulatory document review, and cross-functional team collaboration. WorkSetup: hybrid in Norwood, MA (3 days onsite) or remote with monthly travel.