Clinical Trials Project Manager

Veterans in Healthcare; Los Angeles (CA); On-site; USD 43,000 - 91,000; Full time

Job summary

UCLA Health in Los Angeles is seeking a Project Manager for the Division of Clinical Trials Development to support protocol development, study start-up, and regulatory submissions on investigator-initiated trials.

You will collaborate with investigators, study teams, and monitors to ensure accurate documentation and timely trial procedures, adapting to shifting priorities to maintain smooth operations and high-quality patient outcomes.

Qualifications

• Experience in clinical trials development and management.
• Familiarity with regulatory submissions and study start-up processes.

Responsibilities

• Supports clinical research efforts including protocol development, study start-up, and regulatory submissions for investigator-initiated trials.
• Works with study teams and monitors to ensure accurate, complete, and timely documentation of patient care and study procedures.
• Adapts to study priorities to ensure smooth trial operations and high-quality outcomes.

Job description

Work Location Los Angeles,CA Job #28610 Work Hours Monday through Friday; 8:00am to 5:00pm Employment Type 2 – Staff- Career Duration Indefinite Salary Range $33.09-65.77 Hourly Posted Date August 10, 2026 Bargaining Unit RP – RPSP

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.

The Project Manager (PM) for the Division of Clinical Trials Development (CTD) supports clinical research efforts at UCLA and within the TRIO‑US Network. Under the direction of the CTD Manager, investigators, and Senior Management, the PM contributes to protocol development, study start‑up, and regulatory submissions for investigator‑initiated clinical trials. The role works closely with study teams and monitors to ensure accurate, complete, and timely documentation of patient care and study procedures. Responsibilities may shift based on study priorities, requiring adaptability to ensure smooth trial operations and support high‑quality research and patient‑centered outcomes.

Salary: $31.51 – $62.64 hourly