Clinical Research Coordinator: Study Ops & Compliance

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

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.