Clinical Research Nurse Jobs in Utah
Clinical Research Nurse jobs in Utah are in steady demand, concentrated in academic medical centers, biotech, and pharmaceutical research organizations, with openings at every experience level from staff to principal investigator support. Salt Lake City, Provo, and Ogden are the primary hiring centers, where anchor institutions such as University of Utah Health, Intermountain Health, and Huntsman Cancer Institute consistently recruit. The most sought-after specialties are oncology trials, cardiovascular studies, and Phase II through IV drug research. Scan the live roles below and apply to whichever ones fit.
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Advanced Research Institute has an immediate opening for a Regulatory Coordinator position. The Regulatory Coordinator develops and coordinates the submission of regulatory documents to ensure compliance with all governing requirements. Supports the Principal Investigator and study team ensuring compliance with the IRB, site SOP’s, state, and federal regulations that govern clinical research. Prepares and maintains all regulatory documents as well as submissions to the Institutional Review Board (IRB) including but not limited to: initial IRB submissions, changes in research or site information, safety and deviation reporting, IRB closures. The Regulatory Coordinator will also maintain and accurately file all study related documents within electronic regulatory system as well as paper binders.
Responsibilities:
- Supports all aspects of regulatory compliance. Prepares, facilitates, submits and maintains the process for accurate and timely submission of IRB applications for study start-up, protocol revisions or amendments, administrative changes, changes in subject population, funding, recruitment procedures, site changes, and changes in informed consent.
- Completes, audits, and maintains study records, materials, and databases to ensure compliance with study protocols, FDA, IRB, and site SOP’s.
- Prepares regulatory documents and obtains signatures for FDA 1572’s, Financial Disclosure Forms, Protocol Signature pages, IB acknowledgment of Receipts, Delegation Logs, Training Documents, and other forms.
- Files all correspondence and other important documents in the electronic regulatory system as well as paper-based regulatory binders.
- Communicates with research staff, project sponsors and project staff to ensure accuracy of regulatory documents and submissions.
- Tracks study approvals and expirations to ensure uninterrupted project approval.
- Submits study renewal applications and study progress reports to the IRB.
- Coordinates with study sponsor, investigator, and IRB to complete all study activities from study start-up to study closure.
- Assists investigators and others involved in clinical research with process and policy issues and provides guidance.
- Recommends and implements regulatory process improvements.
- Maintains current knowledge of federal and institutional guidelines and requirements governing research.
- Demonstrates initiative, enthusiasm, positive attitude, teamwork, and commitment to the research mission of Advanced Research Institute.
Disclaimer
This job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to the job.
Job Type/Work Environment:
Full Time. Office environment.
Minimum Qualifications:
One year of regulatory experience with Industry-Sponsored clinical trials is preferred. Current training, certifications, and/or degrees in the field of human research protections is preferred.
Job Type: Full-time
Pay: $18.00 - $26.00 per hour
Benefits:
- 401(k) matching
- Flexible spending account
- Health insurance
- Paid time off
Work Location: In person
Advanced Research Institute has an immediate opening for a Regulatory Coordinator position. The Regulatory Coordinator develops and coordinates the submission of regulatory documents to ensure compliance with all governing requirements. Supports the Principal Investigator and study team ensuring compliance with the IRB, site SOP’s, state, and federal regulations that govern clinical research. Prepares and maintains all regulatory documents as well as submissions to the Institutional Review Board (IRB) including but not limited to: initial IRB submissions, changes in research or site information, safety and deviation reporting, IRB closures. The Regulatory Coordinator will also maintain and accurately file all study related documents within electronic regulatory system as well as paper binders.
Responsibilities:
- Supports all aspects of regulatory compliance. Prepares, facilitates, submits and maintains the process for accurate and timely submission of IRB applications for study start-up, protocol revisions or amendments, administrative changes, changes in subject population, funding, recruitment procedures, site changes, and changes in informed consent.
- Completes, audits, and maintains study records, materials, and databases to ensure compliance with study protocols, FDA, IRB, and site SOP’s.
- Prepares regulatory documents and obtains signatures for FDA 1572’s, Financial Disclosure Forms, Protocol Signature pages, IB acknowledgment of Receipts, Delegation Logs, Training Documents, and other forms.
- Files all correspondence and other important documents in the electronic regulatory system as well as paper-based regulatory binders.
- Communicates with research staff, project sponsors and project staff to ensure accuracy of regulatory documents and submissions.
- Tracks study approvals and expirations to ensure uninterrupted project approval.
- Submits study renewal applications and study progress reports to the IRB.
- Coordinates with study sponsor, investigator, and IRB to complete all study activities from study start-up to study closure.
- Assists investigators and others involved in clinical research with process and policy issues and provides guidance.
- Recommends and implements regulatory process improvements.
- Maintains current knowledge of federal and institutional guidelines and requirements governing research.
- Demonstrates initiative, enthusiasm, positive attitude, teamwork, and commitment to the research mission of Advanced Research Institute.
Disclaimer
This job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to the job.
Job Type/Work Environment:
Full Time. Office environment.
Minimum Qualifications:
One year of regulatory experience with Industry-Sponsored clinical trials is preferred. Current training, certifications, and/or degrees in the field of human research protections is preferred.
Job Type: Full-time
Pay: $18.00 - $26.00 per hour
Benefits:
- 401(k) matching
- Flexible spending account
- Health insurance
- Paid time off
Work Location: In person
See All 17 Clinical Research Nurse Jobs in Utah
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Find Clinical Research Nurse JobsClinical Research Nurse Jobs by City in Utah
Where Utah roles are concentrated, by current openings.
Clinical Research Nurse Job Market in Utah
A snapshot from current Utah openings, updated as new roles post.
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What Utah Employers Look For
The qualifications that appear most often in clinical research nurse jobs across Utah.
- Active Utah Registered Nurse license issued or recognized by the Utah Division of Occupational and Professional Licensing
- Minimum two years of clinical nursing experience in a hospital or research setting
- Experience coordinating or supporting clinical trials under Good Clinical Practice guidelines
- Certification as a Clinical Research Coordinator or Clinical Research Associate preferred
- Proficiency with electronic data capture systems such as REDCap or Medidata Rave
- Strong attention to protocol compliance, adverse event documentation, and regulatory binder maintenance
Clinical Research Nurse Jobs in Utah: Frequently Asked Questions
How do you become a clinical research nurse in Utah?
You must first hold an active Registered Nurse license issued or recognized by the Utah Division of Occupational and Professional Licensing, which requires passing the NCLEX-RN exam. Most Utah employers expect a Bachelor of Science in Nursing, though associates-prepared nurses with strong trial experience are considered for some roles. From there, pursuing a credential such as the Certified Clinical Research Professional or Certified Clinical Research Coordinator strengthens your application considerably within Utah's research community.
Which companies hire clinical research nurses in Utah?
Companies currently hiring clinical research nurses in Utah include University of Utah, ICON, and Advanced Research Institute, per current listings on Migrate Mate as of October 2026. Utah's concentration of academic medical systems and specialty cancer and cardiovascular research programs means many openings sit within large integrated health networks rather than standalone research firms.
Which Utah cities have the most clinical research nurse jobs?
Salt Lake City, Ogden, and Draper lead Utah for clinical research nurse openings. Salt Lake City drives the majority of listings because of its dense cluster of academic medical centers, including University of Utah Health and Huntsman Cancer Institute, while Provo benefits from nearby pharmaceutical and biotech employers, and Ogden sees openings tied to Intermountain Health's regional campuses.
Are there remote clinical research nurse jobs in Utah?
Yes, but they're rare. Clinical research nursing is fundamentally a hands-on role, requiring direct patient contact, specimen handling, and on-site protocol compliance. About 0% of clinical research nurse openings tied to Utah are remote or hybrid as of October 2026, and those tend to be focused on data review, regulatory documentation, or patient follow-up coordination rather than active trial visits.
How can I get hired as a clinical research nurse in Utah with little or no experience?
The most realistic entry path is applying to new graduate or transition programs at large Utah health systems like University of Utah Health or Intermountain Health, both of which run structured residencies and research onboarding tracks. Lateral moves from roles such as oncology staff nurse, infusion nurse, or clinical trials coordinator assistant are common entry points. Completing a Good Clinical Practice certification and volunteering on an IRB-approved study at a Utah academic center strengthens your candidacy before your first dedicated research role.
Where can I find and apply to clinical research nurse jobs in Utah?
You can find and apply to clinical research nurse jobs in Utah on Migrate Mate, which lists current Utah openings in one place. Search the listings for roles that match your experience and specialty, then apply directly to the ones that fit.
See All 17 Clinical Research Nurse Jobs in Utah
Find roles in Utah that match your experience and apply in just a few clicks.
Find Clinical Research Nurse Jobs