PS Study Coordinator III

University of Utah; Salt Lake City (UT); On-site; USD 42,000 - 60,000; Full time

Job summary

The University of Utah is seeking a PS Study Coordinator III to support the Emergency Medicine Contracts department in coordinating research studies on campus. The role involves coordinating technical and administrative aspects, assisting PIs and sponsors, and ensuring protocol implementation aligns with study milestones.

A bachelor’s degree (or equivalent) and several years of related experience are required.

Qualifications

• Equivalency allowed: 1 year of higher education equals 1 year related work experience.
• Study Coordinator III requires a bachelor’s (or equivalency) + 6 years of related work experience, or a master’s (or equivalency) + 4 years.

Responsibilities

• Coordinate technical and administrative details of research studies to support protocol implementation.
• Assist with data management, budget negotiations, and regulatory documentation.
• Ensure accuracy and compliance for successful study outcomes.

Job description

PS Study Coordinator III

This position is patient-sensitive and must fulfill all associatedvaccination requirements, or be approved for an exemption, prior tothe first day of work. We protect our patients, coworkers andcommunity by requiring all patient-sensitive employees to beimmunized according to CDC standards and hospital policy. Limitedexemptions may be made for documented medical contraindications orreligious beliefs that object to vaccinations.

Coordinate technical and administrative aspects of researchstudies, supporting research goals and protocol implementation.Assists with documentation, logistics, budget negotiations, anddata management. Ensures accuracy and compliance for successfulstudy outcomes.

Learn more about the great benefits of working forUniversity of Utah: benefits.utah.edu

Responsibilities

Coordinate technical and administrative details of researchstudies, supporting Principal Investigators in implementingprotocols and procedures. Assess protocol clarity and criteria, andaddress concerns with the PI and sponsor. Participate in meetingsto advise on assignments and timelines. Obtain necessarydocumentation and maintain accurate records. Coordinate facilityand equipment availability as required. Report adverse events anddocument deviations as necessary. Assist with data management,including completing, auditing, and correcting records. Supportbudget negotiations and maintain documentation per regulatoryguidelines. Manage documents and ensure proper specimen handling.Perform additional research support tasks as needed.

Minimum Qualifications

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

Study Coordinator, III: Requires a bachelor's (orequivalency) + 6 years or a master's (or equivalency) + 4 years ofdirectly related work experience.

Requisition Number

PRN46047B

Full Time or Part Time?

Full Time

Work Schedule Summary

Monday – Friday 9:00 AM – 5:00AM

Department

01777 - EMERGENCY MEDICINE CONTRACTS

Location

Campus

Pay Rate Range

$42,000- $60,000

Close Date

09/04/2026