Clinical Research Coordinators (Non-R.N.)

University of Utah Health Research; Salt Lake City (UT); On-site; USD 36,000 - 83,000; Full time

Job summary

The University of Utah Health invites applications for Clinical Research Coordinators (Non-R.N.) to join the Pulmonary department on campus. This patient-sensitive role coordinates day-to-day clinical trial activities in line with GCPs and study protocols.

You will recruit and consent participants, maintain source documents, and liaise with investigators, departments, and external partners. A strong attention to detail and ability to manage multiple studies is essential.

Responsibilities

• Coordinate day-to-day clinical trial activities in adherence to Good Clinical Practices (GCPs) and study protocols.
• Recruit, screen, enroll, and obtain consent from study participants.
• Collect and maintain patient and laboratory data across visits.
• Create and maintain documentation to track study metrics and provide updates to management.
• Work with the PI and liaise with other departments, outside organizations, and government agencies.

Job description

Details
Open Date 10/12/2026
Requisition Number PRN46457B
Job Title Clinical Research Coordinators (Non-R.N.)
Working Title Clinical Research Coordinators (Non-R.N.)
Career Progression Track P00
Track Level P3 - Career
FLSA Code Administrative
Patient Sensitive Job Code? Yes
Standard Hours per Week 40
Full Time or Part Time? Full Time
Shift Day

Work Schedule Summary

VP Area U of U Health - Academics
Department 00239 - Pulmonary
Location Campus
City Salt Lake City, UT
Type of Recruitment External Posting
Pay Rate Range $36,196 to $83,036
Close Date 01/12/2027
Priority Review Date (Note - Posting may close at any time)

Job Summary

Clinical Research Coordinators (Non-R.N.)

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.
We protect our patients, coworkers and community by requiring all patient-sensitive employees to be immunized according to CDC standards and hospital policy.
Limited exemptions may be made for documented medical contraindications or religious beliefs that object to vaccinations.
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).
Learn more about the great benefits of working for University of Utah: benefits.utah.edu
The department may choose to hire at any of the below job levels and associated pay rates based on their business need and budget.

Responsibilities

Clinical Research Coordinator (Non-R.N.), III

Coordinate