
Clinical Research Coordinator
Salt Lake City, UTFull-time$48–89K/yrSeen 2w agoSeen in employer's feed 1w ago
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Job overview
The Clinical Research Coordinator (Non-R.N.) at the University of Utah assists in conducting clinical trials in the ICU, ensuring patient safety, regulatory compliance, and scientific integrity while coordinating with providers, nurses, and study sponsors.
Skills & qualifications
Skills
Qualifications
Benefits
Full job description
Details
Open Date 09/17/2026
Requisition Number PRN46235B
Job Title Clinical Research Coordinators (Non-R.N.)
Working Title Clinical Research Coordinator
Career Progression Track P00
Track Level P5 - Expert, P4 - Advanced, 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 00265 - Cardiothoracic Division
Location Campus
City Salt Lake City, UT
Type of Recruitment External Posting
Pay Rate Range 47,590 - 88,940
Close Date 12/17/2026
Priority Review Date (Note - Posting may close at any time)
Job Summary
Clinical Research Coordinators (Non-R.N.)
Assists in facilitating the conduct of clinical research by performing research and clinical
duties. Provides patient care within the scope of nursing practice and in compliance with
guidelines set by governing agencies. Serve as the clinical champion for a critical care
study, ensuring that the research protocol is seamlessly integrated into daily patient
care while maintaining the highest standards of patient safety, regulatory compliance,
and scientific integrity. Work closely with providers, ICU nurses, advanced practice
providers, research staff, and study sponsors to coordinate complex clinical trial(s)
involving critically ill patients. Actual skills and responsibilities may vary accordingly
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
-
Assesses and ensures subject safety during trial.
-
Proposes and negotiates alternatives for protocol (when allowable). Educates
staff about the scientific aspects of the study, while prioritizing participant
safety and high-quality patient care.
- Perform clinical assessments and monitor participants for adverse events and
protocol compliance. Appliespharmacological knowledge to help PI
determineidiosyncrasies and unexpected results. Evaluates adverse events
(AE), intervenes when necessary and reports details to PI. Conducts
follow-up to determine resolution of AE. Reports serious AEs to IRB and
sponsor.
- Presents related information to the community for recruitment purposes or to
other research professionals in a variety of settings.
-
Mentors and trains new and subordinate employees.
-
Helps determine personnel required to complete the trial and develop the
timeline for trial completion. Reviews study-related data to ensure compliance
with the study protocol.
-
Prepares emergency use report.
-
Manages pharmacokinetic collection and storage.
-
Relates lab results to PI and sponsor.
10.Ensures appropriate maintenance and calibration of equipment.
- May perform bedside care.
Clinical Trial Leadership
-
Primary clinical coordinator assigned to the ICU trial.
-
Anticipate operational challenges and independently develop practical
solutions to maintain study success
- Coordinate participant visits, procedures, laboratory collections, and
follow-up, including screening and recruitment.
- Maintain accurate source documentation and research records in accordance
with GCP , FDA , HIPAA , and IRB requirements.
-
Develops and maintains all study regulatory requirements and logs.
-
Assist with IRB submissions.
-
Ensure compliance with institutional policies, sponsor requirements, and
federal regulations.
Comments
Work Environment and Level of Frequency that may be required:
Nearly Continuously: Daily presence in the ICU and close collaboration with clinical
teams caring for critically ill patients. Office environment.
Often: Infectious disease; oils (including air or skin exposure to oils or other cutting
fluids); hazards (including a variety of physical conditions, such as proximity to moving
mechanical parts, moving vehicles, electrical current, working on scaffolding and high
places, or exposure to chemicals).
Physical Requirements and Level of Frequency that may be required
Nearly continuously: Hearing, listening, talking.
Often: Repetitive hand motion (such as typing), walking, standing, sitting.
Seldom: Bending, reaching overhead.
The staff member must be able to demonstrate the knowledge and skills necessary to
provide age-appropriate care to the patients served on his or her assigned unit. The
individual must demonstrate knowledge of the principles of lifespan growth and
development and the ability to assess patient status data and provide care as described
in the department’s policies and procedures manual
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.), III : Requires a bachelor’s (or equivalency) + 6 years or a master’s (or equivalency) + 4 years of directly related work experience.
Clinical Research Coordinator (Non-R.N.), IV: Requires a bachelor’s (or equivalency) + 8 years or a master’s (or equivalency) + 6 years of directly related work experience.
Clinical Research Coordinator (Non-R.N.), V: Requires a bachelor’s (or equivalency) + 10 years or a master’s (or equivalency) + 8 years of directly related work experience.
Preferences
Type Benefited Staff
Special Instructions Summary
Additional Information
The University is a participating employer with Utah Retirement Systems (“URS”). Eligible new hires with prior URS service, may elect to enroll in URS if they make the election before they become eligible for retirement (usually the first day of work). Contact Human Resources at (801) 581-7447 for information. Individuals who previously retired and are receiving monthly retirement benefits from URS are subject to URS’ post-retirement rules and restrictions. Please contact Utah Retirement Systems at (801) 366-7770 or (800) 695-4877 or University Human Resource Management at (801) 581-7447 if you have questions regarding the post-retirement rules.
This position may require the successful completion of a criminal background check and/or drug screen.
The University of Utah values candidates who have experience working in settings with students and possess a strong commitment to improving access to higher education.
Veterans’ preference is extended to qualified applicants, upon request and consistent with University policy and Utah state law. Upon request, reasonable accommodations in the application process will be provided to individuals with disabilities.
Consistent with state and federal law, the University of Utah does not discriminate based upon race, ethnicity, color, religion, national origin, age, disability, sex, sexual orientation, gender, gender identity, gender expression, pregnancy, pregnancy-related conditions, genetic information, or protected veteran’s status. The University does not discriminate on the basis of sex in the education program or activity that it operates, as required by Title IX and 34 CFR part 106. The requirement not to discriminate in education programs or activities extends to admission and employment. Inquiries about the application of Title IX and its regulations may be referred to the Title IX Coordinator, to the Department of Education, Office for Civil Rights, or both.
To request a reasonable accommodation for a disability or if you or someone you know has experienced discrimination or sexual misconduct including sexual harassment, you may contact the Director/Title IX Coordinator in the Office of Equal Opportunity and Title IX ( OEO ). More information, including the Director/Title IX Coordinator’s office address, electronic mail address, and telephone number can be located at the:University of Utah Non‑Discrimination page.
Online reports may be submitted athttps://oeo.utah.edu
**https://publicsafety.utah.edu/safetyreport/**This report includes statistics about criminal offenses, hate crimes, arrests and referrals for disciplinary action, and Violence Against Women Act offenses. They also provide information about safety and security-related services offered by the University of Utah. A paper copy can be obtained by request at the Department of Public Safety located at 1658 East 500 South.
As perUniversity of Utah policy 5-108: Transfer of Benefits Eligible Staff Members, a new hire to the University of Utah who is still serving a 12 month probationary period will not be hired into another University of Utah job (a transfer) until the successful completion of the probationary period.
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