University of Utah ยท 13 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 is seeking a Trauma Study Coordinator to assist with the logistical and administrative aspects of clinical trials and studies. The role involves participant recruitment, consent processes, documentation management, and ensuring adherence to protocols and regulatory requirements.
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 for Clinical Study Coordinator, I
Requires a bachelor's (or equivalency) + 4 years or a master's (or equivalency) + 2 years of directly related work experience for Clinical Study Coordinator, II
Requires a bachelor's (or equivalency) + 6 years or a master's (or equivalency) + 4 years of directly related work experience for Clinical Study Coordinator, III
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
The University of Utah, located in Salt Lake City in the foothills of the Wasatch Mountains, is the flagship institution of higher learning in Utah.
10001+ employees
H1B Sponsorship
University of Utah has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (216)
2024 (189)
2023 (201)
2022 (175)
2021 (156)
2020 (174)
Funding
Current Stage
Late StageLeadership Team
Allison Nicholson
Special Assistant to CFO
Bruce Hunter
Interim Chief Innovation and Economic Engagement Officer
Recent News
National Institutes of Health (NIH)
2023-06-27
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