University of Utah · 5 hours ago
Clinical Research Coordinators (Non-R.N.)
Salt Lake City, UT
Full-time
Onsite
Mid Level
$30K/yr - $69K/yr
4+ years expUniversity of Utah is seeking Clinical Research Coordinators (Non-R.N.) to coordinate day-to-day clinical trial activities while adhering to Good Clinical Practices and study protocols. The role involves recruiting participants, maintaining documentation, and working under the direction of the Primary Investigator.
Higher Education
Responsibilities
Coordinate day-to-day clinical trial activities in adherence to Good Clinical Practices (GCPs), study protocols, and applicable regulations
Implement processes and organize efforts within study team to achieve objectives, coordinating research procedures, study visits, and follow-up care
Create and maintain tools and documentation to track study metrics, providing updates to management
Conduct pre-study, site qualification, study initiation, monitoring visits, and close-out activities
Maintain source documents and report adverse events
Recruit, screen, enroll, and obtain consent from study participants
Collect and maintain patient and laboratory data
Work directly with study participants and families and serve as project liaison to other departments, outside organizations, and government agencies
Works under the direction of the Primary Investigator (PI)
Requires moderate skill set and proficiency in discipline
Conducts work assignments of increasing complexity, under moderate supervision with some latitude for independent judgment
Qualification
Required
This position is patient-sensitive and must fulfill all associated vaccination requirements, or be approved for an exemption, prior to the first day of work
Coordinate day-to-day clinical trial activities in adherence to Good Clinical Practices (GCPs), study protocols, and applicable regulations
Implement processes and organize efforts within study team to achieve objectives, coordinating research procedures, study visits, and follow-up care
Create and maintain tools and documentation to track study metrics, providing updates to management
Conduct pre-study, site qualification, study initiation, monitoring visits, and close-out activities
Maintain source documents and report adverse events
Recruit, screen, enroll, and obtain consent from study participants
Collect and maintain patient and laboratory data
Work directly with study participants and families and serve as project liaison to other departments, outside organizations, and government agencies
Work under the direction of the Primary Investigator (PI)
Requires a bachelor's (or equivalency) + 4 years or a master's (or equivalency) + 2 years of directly related work experience
1 year of higher education can be substituted for 1 year of directly related work experience
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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