Study Coordinator – Neurology

Veterans in Healthcare; Los Angeles (CA); Sur place; USD 53 000 - 85 000; Plein temps

Résumé du poste

UCLA Health is seeking a Clinical Research Coordinator to manage study activities from design through closeout at the Los Angeles location. You will oversee trial operations, ensure protocol compliance, and coordinate with principal investigators and sponsors to advance multiple studies.

The role emphasizes experienced leadership in research execution, regulatory adherence, and collaboration across departments to optimize study performance and outcomes.

Qualifications

• Experience in clinical research project management or coordination.

Responsabilités

• Oversee operational management of clinical research activities from design to closeout.
• Ensure protocol compliance and timely execution of study procedures.
• Collaborate with PIs, sponsors, and departments to support administration of studies.

Description du poste

Work Location Los Angeles,CA Job #32377 Work Hours Monday-Friday 8am-5pm Employment Type 2 – Staff- Career Duration Indefinite Salary Range $38.19-61.45 Hourly Posted Date August 11, 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.

• JOB DUTIES
• JOB QUALIFICATIONS

Description The Clinical Research Coordinator plays a critical role in the overall operational management of clinical research/trial/study activities from design, set up, conduct, through closeout. The incumbent is an experienced professional or leader who has direct responsibility for the implementation of research activities for one or more studies which may include multicenter clinical trials (both NIH and industry-sponsored), local investigator-initiated clinical trials, and/or programmatic clinical research activities. The incumbent recognizes and performs necessary project management tasks and prioritizes work to reach scheduled goals. The incumbent is a technical leader responsible for ensuring the study protocol and procedures have been completed accurately, safely, and in a timely manner. This position may supervise and train others on projects as necessary. The incumbent works with PIs, departments, sponsors, institutions, and other entities as needed to support and provide guidance on the administration of the compliance, financial, personnel and other related aspects of studies. Hourly salary range: 38.19 – 61.45.