University of Utah ยท 3 weeks ago
Clinical Research Coordinators (Non-R.N.)
Salt Lake City, UT
Full-time
Onsite
Mid, Senior Level
$30K/yr - $83K/yr
4+ years expUniversity of Utah is seeking Clinical Research Coordinators (Non-R.N.) to coordinate day-to-day clinical trial activities. The role involves managing processes to support study objectives, maintaining documentation, and conducting various research-related activities under the direction of the Lead Study Coordinator and Primary Investigators.
Higher Education
Responsibilities
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)
Qualification
Required
Requires a bachelor's (or equivalency) + 4 years or a master's (or equivalency) + 2 years of directly related work experience for Clinical Research Coordinator (Non-R.N.), II
Requires a bachelor's (or equivalency) + 6 years or a master's (or equivalency) + 4 years of directly related work experience for Clinical Research Coordinator (Non-R.N.), III
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)
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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