Clinical Research Coordinator I

Schedule: Monday-Friday; 8:00am-5:00pm Purpose Statement/Position Summary: The Clinical Research Coordinator supports principal investigators and research teams in the conduct of clinical research studies by coordinating and managing study activities throughout the research lifecycle. Responsibilities include reviewing and adhering to clinical research protocols; assisting with participant recruitment, enrollment, scheduling, and follow-up; coordinating specimen collection, processing, shipment, and storage; managing study treatment logistics and follow-up activities as applicable; and collecting, extracting, and reporting study data from electronic medical records and source documents using paper and electronic data capture systems. The role also supports safety reporting, regulatory compliance activities, and Institutional Review Board (IRB) submissions, including new study applications, amendments, continuing reviews, and study closeouts. Additional responsibilities include maintaining regulatory binders and study documentation, supporting study startup activities such as budgets, contracts, medical coverage analyses, ancillary department approvals, and regulatory submissions, as well as processing study invoicing and ensuring adherence to institutional, sponsor, and regulatory requirements. Required Minimum Qualifications/Work Experience: 1+ year experience in clinical trial coordination or computerized databases. Education/Licensure/Certifications Required: High School Diploma Preferred Bachelor's degree or Associate degree in related scientific field. Certified clinical research associate/coordinator preferred. #J-18808-Ljbffr Children's Hospital Los Angeles (CHLA)