Senior Clinical Research Coordinator

Job Summary

Senior Clinical Research Coordinator

Coordinate day‑to‑day operations of clinical trials following GCP, study protocols, and regulations. Organize processes and study team activities to meet research objectives. Manage study visits, research procedures, and follow‑up. Develop and maintain tracking tools and documentation; report study metrics to management. Support all stages of study visits: pre‑study, qualification, initiation, monitoring, and close‑out. Maintain source documentation and report adverse events. Recruit, screen, consent, and enroll participants. Collect and maintain patient and lab data. Act as liaison among participants, families, departments, external organizations, and government agencies. Work under direction of the Principal Investigator.

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.), IV
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). Recognized as subject matter expert and advanced individual contributor professional. Requires specialized skill set. Conducts highly complex work, unsupervised and with extensive latitude for independent judgment.

Requires a bachelor's (or equivalency) + 8 years or a master's (or equivalency) + 6 years of directly related work experience.This is an Advanced-Level position in the General Professional track.Job Code: PZ6514Grade: P16

Minimum Qualifications

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).

Department may hire employee at one of the following job levels:

Clinical Research Coordinator (Non-R.N.), IV: Requires a bachelor's (or equivalency) + 8 years or a

Preferences

Bachelor's degree + 8 years of directly related experience OR Master's degree + 6 years of directly related experience. Education can substitute for experience on a 1:1 basis.

Special Instructions

Requisition Number: PRN44360B
Full Time or Part Time? Full Time
Work Schedule Summary: M-F
Department: 00269 - Orthopedic Surgery Operations
Location: Campus
Pay Rate Range: $60K-$80K
Close Date: 3/31/2026
Open Until Filled: