Clinical Trials Manager

Role: Lead clinical operations for domestic and global studies at Neurocrine Biosciences, ensuring compliance and smooth execution across therapeutic areas. Responsibilities: oversee planning, initiation, conduct, and close-out of clinical trials; manage CROs and internal teams; develop study timelines, monitor budget, and address enrollment barriers; participate in protocol design and study reports; enforce GxP standards and regulatory compliance (FDA, ICH, EU). Requirements: BS/BA with 6+ years or Master’s with 4+ years in clinical trial management, including vendor oversight; strong knowledge of drug development processes, GCP, FDA/EU regulations; experience managing clinical studies from start-up to close-out; excellent project management, communication, problem-solving, and leadership skills. Preferred: experience with neuroscience or neurological indications, and broad trial management expertise. HighValue: extensive CRO/vendor management, international trials, GxP compliance, protocol development, and cross-functional collaboration. WorkSetup: Not specified, but likely hybrid or onsite based on role scope.