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Stanford University is seeking an Assistant Clinical Research Coordinator to provide administrative support for the collection of clinical data and coordination of clinical studies. You will work under supervision of the principal investigator and study coordinator.
The role involves scheduling, screening, consent processes, data entry, and regulatory documentation to ensure study quality and compliance. Candidates should have a two-year degree and relevant experience, with progress toward
Stanford University is seeking an Assistant Clinical Research Coordinator to perform administrative support duties related to the collection of clinical data and/or the coordination of clinical studies. Work under supervision of the principal investigator and/or study coordinator/supervisor.
Clinical Research Coordinators (CRCs) support, conduct, coordinate or manage the clinical research studies or trials on human subjects. Principal and co-investigators provide the overall direction in a clinical study, but CRCs can have significant roles in clinical study activities.
Two-year college degree and one year of relevant experience or an equivalent combination of experience, education, and training.
Working toward certification(s) to perform basic patient measurements and tests, such as phlebotomy and EKG.
Must possess and maintain a valid California non-commercial Class C Driver's License, if applicable.