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UCLA Health seeks a Clinical Research Coordinator to support the full lifecycle of clinical studies, from design through closeout.
You will implement research activities for one or more studies and organize tasks to ensure adherence to study protocols and regulatory requirements. The role involves collaboration with the Principal Investigator, ancillary departments, sponsors, and other entities to maintain compliant conduct and proper study administration.
The Clinical Research Coordinator contributes to the overall operational management of clinicalresearch/trial/study activities from design, set up, conduct, through closeout. In this role, you will beresponsible for the implementation of research activities for one or more studies. Perform necessarytasks to manage projects and prioritizes work to meet necessary deadlines. You will be responsible forplanning and organizing necessary tasks to ensure adherence to the study protocol and applicableregulations, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), andICH Good Clinical Practice (GCP). The Clinical Research Coordinator collaborates with the PrincipalInvestigator (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 notlimited to, compliant conduct, financial management, and adequate personnel support.
Hourly salary range: $38.19 - $61.45