Clinical Research Coordinator

UCLA Health; Los Angeles (CA); On-site; USD 53,000 - 85,000; Full time

Job summary

UCLA Health is seeking a Study Coordinator to manage clinical research activities from start-up through close-out. You will coordinate study operations for one or more protocols to keep projects on schedule and compliant.

Working with Principal Investigators, sponsors, and research teams, you’ll support regulatory compliance and financial management, ensuring adherence to GCP, FDA regulations, and institutional policies. Salary: $38.19 - $61.45 hourly.

Responsibilities

• Coordinate day-to-day study operations across one or more research protocols.
• Support regulatory compliance, study conduct, and financial management according to GCP, FDA regulations, and institutional policies.

Job description

Description

The Study Coordinator plays a central role in the successful management of clinical research studies from start up through closeout. The position is responsible for implementing and coordinating study activities for one or more research protocols, ensuring projects are completed efficiently, on schedule, and in compliance with all applicable requirements.

Working closely with Principal Investigators (PIs), sponsors, research teams, and institutional partners, the Study Coordinator manages day to day study operations, supports regulatory compliance, and helps ensure adherence to study protocols, institutional policies, FDA regulations, and ICH Good Clinical Practice (GCP) guidelines. The role requires strong organizational, project management, and communication skills to coordinate multiple priorities while supporting compliant study conduct, financial management, and overall research success.

Salary: $38.19 - $61.45 hourly