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UCLA Health in Santa Monica seeks a Clinical Research Coordinator to manage the operational aspects of study lifecycles, from design through closeout. You will implement activities to meet timelines while ensuring compliance with study protocols, CFR, and ICH-GCP, coordinating with the Principal Investigator and sponsors.
The role emphasizes collaboration with ancillary departments and central research teams to support compliant conduct, financial management, and adequate staffing, with an
The Clinical Research Coordinator supports the operational management of clinical research activities throughout the study lifecycle, including design, start-up, conduct, and closeout. This role is responsible for implementing and managing research activities for one or more studies, prioritizing tasks to meet required deadlines. The Coordinator plans and organizes study activities to ensure compliance with study protocols and applicable regulations, including institutional policies, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP). The role involves close collaboration with the Principal Investigator, ancillary departments, central research teams, sponsors, and external institutions to support compliant study conduct, financial management, and adequate staffing.
Hourly salary range: $38.19 - $61.45