Details
Open Date
10/24/2025
Requisition Number
PRN43410B
Job Title
Research Coordinators (Non-R.N.)
Working Title
Research Coordinator VII (Non-R.N.)
Career Progression Track
P00
Track Level
P7 - Senior Principal
FLSA Code
Administrative
Patient Sensitive Job Code?
No
Standard Hours per Week
20
Full Time or Part Time?
Part Time
Shift
Day
Work Schedule Summary
This position is part time.
VP Area
U of U Health - Academics
Department
00870 - Ophthalmology-Research
Location
Campus
City
Salt Lake City, UT
Type of Recruitment
External Posting
Pay Rate Range
$95,000 - $115,000
Close Date
01/24/2026
Priority Review Date (Note - Posting may close at any time)
Job Summary
Coordinate day-to-day research activities in adherence to Responsible Conduct for Research ( RCR ), study protocols, and applicable regulations. Implement processes and organize efforts within study team to achieve objectives, coordinate activities, and support research study initiation and close out. Conduct pre-study site visits, monitoring or other site visits at locations or sites participating in the study. Create and maintain tools and documentation to track study procedures, protocols and metrics, providing updates to management. Maintain source documents and report adverse events. Recruit, screen, enroll, and obtain consent from study participants. Collect and maintain study participant data and other forms of study data. Work directly with study participants and serve as project liaison to other departments, outside organizations, and government agencies. Works under the direction of the Primary Investigator (PI) or Project Director (PD). Requires highly specialized skill set. Influences best practices within discipline. Conducts the most complex and vital work, unsupervised and with complete latitude for independent judgment.
Learn more about the great benefits of working for University of Utah: benefits.utah.edu
Responsibilities
Coordinate day-to-day research activities in adherence to Responsible Conduct for Research ( RCR ), study protocols, and applicable regulations. Implement processes and organize efforts within study team to achieve objectives, coordinate activities, and support research study initiation and close out. Conduct pre-study site visits, monitoring or other site visits at locations or sites participating in the study. Create and maintain tools and documentation to track study procedures, protocols and metrics, providing updates to management. Maintain source documents and report adverse events. Conduct pre-study, site qualification, study initiation, monitoring visits, and close-out activities. Recruit, screen, enroll, and obtain consent from study participants. Collect and maintain study participant data and other forms of study data. Work directly with study participants and serve as project liaison to other departments, outside organizations, and government agencies. Works under the direction of the Primary Investigator (PI) or Project Director (PD). Requires highly specialized skill set. Influences best practices within discipline. Conducts the most complex and vital work, unsupervised and with complete latitude for independent judgment.
Minimum Qualifications
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