Clinical Trial Manager

Role: Clinical Trial Manager overseeing Phase I-III oncology studies, responsible for vendor management, trial execution, compliance, and documentation. Responsibilities: lead CRO oversight, develop study protocols and monitoring plans, manage investigator sites, ensure adherence to GCP and FDA regulations, and support safety and data integrity; collaborate with cross-functional teams and external vendors. Requirements: BS or MS with 5+ years industry experience in clinical operations, oncology trial management preferred; strong knowledge of FDA, ICH, and GCP; vendor management expertise; excellent communication skills; ability to travel (~25%). HighValue: Oncology, Phase I-III trials, early-stage development, CRO/vendor oversight, global trial experience including APAC. WorkSetup: onsite Redwood City, CA, with travel.