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UCLA Health is seeking an Assistant Clinical Research Coordinator (ACRC) to support the operational management of clinical studies from design through closeout. The role coordinates study activities, prioritizes tasks, and ensures adherence to study protocols, institutional policies, CFR, and ICH GCP.
You will collaborate with the PI, ancillary departments, sponsors, and research staff to support compliant conduct, financial management, and adequate personnel resources to accommodate varying
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.
*Note: Skills may be subject to test.
Salary Range: $30.74 - 49.46 Hourly