Assistant Clinical Research Coordinator – Hematology/Oncology

Veterans in Healthcare; Los Angeles (CA); On-site; USD 42,000 - 68,000; Full time

Job summary

UCLA Health in Los Angeles, CA is seeking an Assistant Clinical Research Coordinator to manage and coordinate clinical research activities across one or more studies. You will ensure protocol adherence, regulatory compliance, and collaboration with the PI and multidisciplinary teams.

The role involves supporting study setup, conduct, and closeout, coordinating tasks to meet deadlines, and assisting with financial and personnel aspects of trials.

Qualifications

• The Assistant Clinical Research Coordinator coordinates research activities for one or more studies.
• Ensures adherence to study protocol, regulatory requirements, and ICH-GCP.
• Collaborates with the Principal Investigator, central research teams, sponsors, and other stakeholders.

Responsibilities

• Coordinate design, setup, conduct, and closeout of clinical research activities.
• Manage study tasks, timelines, and resources to meet deadlines.
• Support financial management and personnel needs related to studies.

Job description

Work Location Los Angeles,CA Job #33092 Work Hours Monday – Friday, 8:00am – 5:00pm Employment Type 2 – Staff- Career

Duration indefinite Salary Range $- Posted Date September 16, 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.

Description

The Assistant Clinical Research Coordinator (ACRC) contributes to the overall operational management of clinical research/trial/study activities from design, set up, conduct, through closeout. The position has responsibility for the coordination of research activities for one or more studies. The ACRC recognizes and performs necessary tasks to coordinate projects and prioritizes work to meet necessary deadlines. The ACRC participates in planning and organizing necessary tasks to ensure adherence to the study protocol and applicable regulations, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP). The Study Coordinator collaborates with the Principal Investigator (PI), ancillary departments, central research infrastructure teams, sponsors, institutions, and other entities as needed to support the administration of all aspects of studies, including, but not limited to, compliant conduct, financial management, and adequate personnel support. Performance of duties and tasks will vary based on the department operations, the type of study and scope of service. Salary Range: $30.74 – 49.46 Hourly