Geriatrics Assistant Clinical Research Coordinator – 50% Limited

Veterans in Healthcare; Los Angeles (CA); On-site; USD 37,000 - 60,000; Full time

Job summary

UCLA Health in Los Angeles is seeking a clinical research support professional to assist with one or more studies. The role involves coordinating participant visits, data collection, and study documentation within a fast-paced, team-oriented environment.

This limited-duration position (3 months) offers hands-on experience supporting regulatory compliance, study operations, and patient-focused research, with schedules aligned to study timelines and site needs.

Responsibilities

• Support the implementation and coordination of one or more clinical research studies.
• Assist with participant recruitment, study visits, data collection, and study documentation.
• Help organize and prioritize study activities to meet project timelines and research objectives.
• Support regulatory compliance by maintaining study records and adhering to protocol and institutional requirements.
• Collaborate with research teams to ensure accurate, efficient, and compliant study operations.
• Contribute to the successful conduct of clinical research in a fast paced, team oriented environment.

Job description

Work Location Los Angeles,CA Job #34008 Work Hours Monday: 10:00am – 12:00pm and W-F: 9:00am – 3:30pm with 30 minutes meal break Employment Type 4 – Staff- Limited Duration 3 months Salary Range $27.08-43.55 Hourly Posted Date November 6, 2026 Bargaining Unit UPTE – RX

Find the cures you know are out there. At UCLA Health, you make it happen as part of a groundbreaking Research team, working to understand hundreds of medical disorders and improving processes for dozens of procedures across the globe.

Key Responsibilities

• Support the implementation and coordination of one or more clinical research studies.
• Assist with participant recruitment, study visits, data collection, and study documentation.
• Help organize and prioritize study activities to meet project timelines and research objectives.
• Support regulatory compliance by maintaining study records and adhering to protocol and institutional requirements.
• Collaborate with research teams to ensure accurate, efficient, and compliant study operations.
• Contribute to the successful conduct of clinical research in a fast paced, team oriented environment.

This position is an excellent opportunity for individuals interested in building a career in clinical research while gaining hands on experience supporting innovative studies and advancing patient focused research. Note, this is a limited position, which may convert to career. Salary: $27.08 – $43.55 hourly