Clinical Research Coordinator - Pediatrics

Overview The Clinical Research Coordinator (CRC) contributes to the operational management of clinical research/trial/study activities from design, setup, conduct, through closeout. The CRC is responsible for the implementation of research activities for one or more studies and prioritizes work to meet deadlines. The CRC plans and organizes necessary tasks to ensure adherence to the study protocol and applicable regulations, such as institutional policy and procedures, FDA 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 department operations, the type of study and scope of service. Salary Range: $38.19 – $61.45 Hourly Responsibilities Manage clinical research activities from design and setup through conduct and closeout for one or more studies. Implement research activities in accordance with the study protocol and applicable regulations (institutional policies, FDA CFR, ICH GCP). Plan, organize, and prioritize tasks to meet deadlines and ensure compliant conduct and adequate personnel support. Collaborate with the Principal Investigator (PI), ancillary departments, central research infrastructure teams, sponsors, institutions, and other entities as needed. Support administration of all aspects of studies, including financial management and compliance. #J-18808-Ljbffr UCLA Outpatient Clinics