Clinical Research Coordinator: Trials & Compliance Pro

Stanford University is seeking a Clinical Research Coordinator Associate to manage multiple protocols at Stanford Hospital and Clinics. You will work with a team of investigators to prepare IRB submissions, aid amendments and renewals, recruit and consent participants, and maintain data files per GCP and HIPAA guidelines. The role involves data collection, blood sample handling, drug accountability, and reporting adverse events to investigators and sponsors. Evening/weekend hours may be required. #J-18808-Ljbffr Stanford University