Clinical Research Jobs in Utah
Clinical Research jobs in Utah are in strong demand, with the state's life sciences corridor anchoring a concentrated hiring market for coordinators, associates, and study managers at every experience level. Salt Lake City, Provo, and Ogden lead in openings, where organizations like Intermountain Health, the University of Utah Health, and Recursion Pharmaceuticals maintain active clinical operations across oncology, cardiovascular, and rare disease trials. Regulatory affairs and data management are among the most sought-after specialties as Utah's biotech sector continues expanding. 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 Jobs in Utah
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Find Clinical Research JobsClinical Research Jobs by City in Utah
Where Utah roles are concentrated, by current openings.
Clinical Research Job Market in Utah
A snapshot from current Utah openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Education
What Utah Employers Look For
The qualifications that appear most often in clinical research jobs across Utah.
- Bachelor's degree in life sciences, nursing, or a closely related field required
- ACRP or SOCRA certification preferred or required by most Utah research sites
- Experience with FDA regulations, GCP guidelines, and IRB submission processes
- Proficiency in clinical trial management systems such as Medidata or Veeva Vault
- Strong attention to detail for data collection, protocol adherence, and source document verification
- Ability to coordinate with multi-site teams and communicate clearly with investigators and sponsors
Clinical Research Jobs in Utah: Frequently Asked Questions
How do you become a clinical research in Utah?
Most Utah clinical research positions require a bachelor's degree in a life science, health, or related field, followed by industry-recognized certification. The Association of Clinical Research Professionals and the Society of Clinical Research Associates both offer credentials widely recognized by Utah employers. Many coordinators start by gaining experience through hospital-based research departments or academic medical centers like the University of Utah before pursuing the CCRC or CCRP exam.
Which companies hire clinical researchs in Utah?
Employers hiring clinical researchs in Utah right now include University of Utah, ICON, and Advanced Research Institute, based on current listings on Migrate Mate as of October 2026. Utah's integrated health systems and growing biotech companies tend to hire year-round, particularly for oncology and rare disease studies.
Which Utah cities have the most clinical research jobs?
Salt Lake City, Ogden, and Draper have the most clinical research openings in Utah. Salt Lake City anchors the market through Intermountain Health and the University of Utah Health's research programs, while Provo's concentration of biotech and pharmaceutical companies and Ogden's regional hospital systems drive demand in those areas.
Are there remote clinical research jobs in Utah?
Yes, but they're limited. Most clinical research roles involve on-site patient interaction, trial monitoring, and document handling that require physical presence. About 0% of clinical research openings tied to Utah are remote or hybrid as of October 2026, with the remote opportunities concentrated in data management, regulatory affairs, and remote site monitoring positions.
How can I get hired as a clinical research in Utah with little or no experience?
The most realistic entry path is applying for a clinical research coordinator I or research assistant role at a hospital-based research department. Intermountain Health and University of Utah Health both run structured research programs that hire candidates with a relevant degree and no prior trial experience. A completed GCP training certificate and any volunteer or internship exposure to IRB processes gives candidates a meaningful edge in Utah's competitive entry-level market.
Where can I find and apply to clinical research jobs in Utah?
You can find and apply to clinical research jobs in Utah on Migrate Mate, which lists current Utah openings across the state. Search the available roles, find the positions that match your experience and preferred location, and apply directly to the ones that fit.
See All 17 Clinical Research Jobs in Utah
Find roles in Utah that match your experience and apply in just a few clicks.
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