Clinical Research Coordinators (Non-R.N.) jobs in United States
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University of Utah ยท 15 hours ago

Clinical Research Coordinators (Non-R.N.)

University of Utah is seeking Clinical Research Coordinators (Non-R.N.) to coordinate day-to-day clinical trial activities. This role involves adhering to Good Clinical Practices, managing study protocols, and working closely with study participants and families while serving as a liaison with various departments and organizations.

Higher Education
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H1B Sponsor Likelynote

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)
Considered highly skilled and proficient in discipline
Conducts complex, important work under minimal supervision and with wide latitude for independent judgment

Qualification

Clinical PracticesClinical trial coordinationPatient recruitmentData collectionDocumentation managementCommunication skillsTeam collaboration

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) + 6 years or a master's (or equivalency) + 4 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

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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.

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 Stage

Leadership Team

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Allison Nicholson
Special Assistant to CFO
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Bruce Hunter
Interim Chief Innovation and Economic Engagement Officer
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