University of Utah Health Research · 10 hours ago
Trauma Study Coordinator
Salt Lake City, UT
Full-time
Onsite
Entry, Mid, Senior Level
$45K/yr - $58K/yr
2+ years expUniversity of Utah Health Research is seeking a Trauma Study Coordinator to assist with the logistical and administrative aspects of clinical trials and studies. The role involves facilitating participant recruitment, managing documentation, and ensuring adherence to protocols and regulatory requirements for successful study outcomes.
Higher Education
Responsibilities
Helps with the logistical and administrative aspects of clinical trials and studies, ensuring adherence to protocols and regulatory requirements
Help facilitate participant recruitment, consent processes, and documentation management
Coordinate study visits, monitor adverse events, and maintain accurate records for successful study outcomes
Coordinate fundamental technical and administrative details in clinical trials or research studies with some supervision
Assist Principal Investigators in achieving study objectives by implementing and completing study protocols and procedures
Review protocols for clarity and subject safety, addressing concerns with the PI and sponsor
Participate in recruitment and consent processes
Maintain detailed and accurate study documentation
Coordinate study visits and ensure the availability of necessary resources
Report and track adverse events with guidance
Complete and audit CRFs for accuracy
Assist in preparing and submitting IRB documents
Ensure proper collection, processing, and shipment of specimens
Coordinate technical and administrative details of clinical trials or research studies, assisting Principal Investigators in implementing and completing study protocols and procedures
Assess protocol clarity and subject safety, review inclusion/exclusion criteria, and address concerns with the PI and sponsor
Participate in meetings, advising on assignments and timelines
Obtain informed consent, medical history, and demographics, and maintain accurate documentation
Coordinate facility and equipment availability for study visits
Report adverse events, including serious AEs, to the IRB and sponsor
Document protocol deviations, reconcile test article accountability, and prepare summary reports
Complete, audit, correct, and relay CRFs to the sponsor
Assist with negotiating contract budgets and terms, maintain documents per FDA guidelines, manage IRB documents, and ensure proper specimen collection, processing, and shipment
Perform Clinical Research Assistant functions as needed
Qualification
Required
Requires a bachelor's (or equivalency) + 2 years of directly related work experience or a master's (or equivalency) degree
Requires a bachelor's (or equivalency) + 4 years or a master's (or equivalency) + 2 years of directly related work experience
Requires a bachelor's (or equivalency) + 6 years or a master's (or equivalency) + 4 years of directly related work experience
Preferred
A bachelor's (or equivalency) with up to 2 years of directly related work experience or a master's (or equivalency) degree
Company
University of Utah Health Research
At University of Utah Health, our world-class researchers work together to tackle some of the toughest problems in health and medicine.
5001-10000 employees
Funding
Current Stage
Late StageCompany data provided by crunchbase