Clinical Research Coordinators; Non-R.N

Job Summary

The Clinical Research Coordinator will coordinate the implementation, quality control and completion of research studies while assisting the Principal Investigator in determining and accomplishing study objectives. Oversee research studies in an administrative and operational capacity while maintaining compliance with guidelines set by governing agencies. Assist in coordinating research with national and federal grants. Work with outside vendors to coordinate payment to research participants from all over the world, as well as assist in maintaining the study website.

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.

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.

Requires a bachelor’s (or equivalency) + 6 years or a master’s (or equivalency) + 4 years of directly related work experience. This is a Career‑Level position in the General Professional track. Job Code: PZ6513;
Grade: P15.

EQUIVALENCY STATEMENT: 1 year of higher education can be substituted for 1 year of directly related work experience (Example: bachelor’s degree = 4 years of directly related work experience).

Clinical Research Coordinator (Non‑R.N.), III:
Requires a bachelor’s (or equivalency) + 6 years or a master’s (or equivalency) + 4 years of directly related work experience.

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• Requisition Number: PRN
  44334B
• Employment Type:
  
  Full Time
• Work Schedule:
  
  Monday–Friday
• Department: 00269 – Orthopedic Surgery Operations
• Location:
  
  Campus
• Pay Rate Range: $63,775
• Close Date: 3/24/2026