Description
The Protocol Coordinator supports clinical research studies by determining patient eligibility, coordinating study visits and follow-up, managing investigational drugs and blood specimens, recording toxicities and adverse events, maintaining protocol compliance, and supporting data collection and reporting. The role requires an experienced registered nurse, a bachelor’s degree, current California licensure, clinical research experience, and completion of required training. It is an hourly position with a range of $50.13 to $62.89.
