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Clinical Research Coordinators (Non-R.N.)Coordinate day-to-day clinical trial activities in compliance with Good Clinical Practice (GCP), study protocols, and applicable IRB regulations. Implement and manage processes to support study objectives, including development and maintenance of IRB protocols, coordination of research procedures, study visits, and follow-up care. Create and maintain tracking tools and documentation to monitor study metrics and provide regular updates to management.Conduct pre-study, site qualification, study initiation, monitoring, and close-out activities. Maintain accurate source documentation and report adverse events in accordance with regulatory requirements. Recruit, screen, enroll, and obtain informed consent from study participants. Collect, manage, and maintain patient and laboratory data.Work directly with study participants and their families and serve as a liaison to internal departments, external organizations, and government agencies. Perform all duties under the direction of the Lead Study Coordinator and Primary Investigators (PI).This Role will help support the Craig H Neilsen Rehab Research Group. Grant funding is available to support this position.This is an in-person position with some hybrid options available with prior consultation with supervisor.Learn more about the great benefits of working for University of Utah: benefits.utah.eduThe department may choose to hire at any of the below job levels and associated pay rates based on their business need and budget.