
This Specialist, Clinical Trials role supports the operational activities for planning, initiating, conducting, and closing domestic and global clinical studies within Neurocrine Biosciences' clinical operations team. Key responsibilities include managing essential document collection, overseeing IRB and Ethics Committee submissions, coordinating with Contract Research Organizations and investigator sites, and ensuring compliance with FDA regulations and Good Clinical Practices. The position also involves maintaining electronic trial master files and assisting with study timelines and recruitment efforts. The role is appealing for its opportunity to contribute to a mission-driven culture focused on relieving suffering for patients with neurological disorders. It offers a collaborative environment where employees can develop project management skills while working on life-changing treatments. The position is based in San Diego with hybrid work flexibility.




















