Clinical Research Associate Jobs in Utah
Clinical Research Associate jobs in Utah concentrate in clinical trials management, pharmaceutical research, and medical device studies, with hiring demand driven by the state's growing life sciences corridor. Salt Lake City, Provo, and Ogden are the primary hiring markets, where employers such as University of Utah Health, Recursion Pharmaceuticals, and IHC Health Services maintain ongoing clinical research operations. Monitoring, regulatory documentation, and oncology trials are among the most in-demand specialties for this role across Utah. Scan the live roles below and apply to whichever ones fit.
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Job Description Summary: The Clinical Research Coordinator (CRC) works under the direction of company administration and the principle investigator to perform assigned and delegated duties associated with the execution of clinical research trial protocols. The Clinical Research Coordinator will have, or will develop, skills in phlebotomy, electrocardiograms, collection of medical/surgical histories, basic laboratory tests, performance of subject trial visits, completion of case report forms (CRFs), and resolution of data queries. The Clinical Research Coordinator will participate in the completion of regulatory documents. The Clinical Research Coordinator shall have the highest moral and ethical standards and will be expected to conduct themselves in a responsible, professional, moral, and ethical manner at all times. The Clinical Research Coordinator shall have excellent interpersonal communication skills and have a strong commitment to the success of the research team.
Clinical Research Coordinator Responsibilities:
- Assist in the coordination and execution of clinical drug trials under the guidance and direction of the site administrator, principal investigator, and sub-investigators.
- Read, comprehend, and execute clinical trial protocols.
- Perform laboratory tests as required by trial protocol.
- Monitor clinical and laboratory data for accuracy and compliance with trial protocols.
- Complete all documentation required by trial protocol for submission to the trial sponsor.
- Comply with all international, federal, state, local, and company guidance, laws, regulations, policies, and procedures as applicable to clinical research trials and Advanced Research Institute.
- Interact with patients by explaining trial protocols, consenting subjects, monitoring their compliance with protocols, collecting data, and collection laboratory samples.
- Protect every subject's safety to the best of your ability.
- Maintain every patient's rights to privacy.
- Maintain flexibility by performing all other assigned duties.
Training: On the job training. Formal continuing education opportunities provided.
Experience Requirements: Experience is highly preferred but not necessarily required.
Education Requirements: High school diploma required.
Keywords: MA, CNA, Phlebotomist, Research Assistant, Medical Scribe
Job Type: Full-time
Pay: $20.00 - $28.00 per hour
Benefits:
- 401(k) matching
- Dental insurance
- Health insurance
- Paid time off
Experience:
- Clinical research: 1 year (Preferred)
Ability to Commute:
- Sandy, UT 84092 (Required)
Work Location: In person
Job Description Summary: The Clinical Research Coordinator (CRC) works under the direction of company administration and the principle investigator to perform assigned and delegated duties associated with the execution of clinical research trial protocols. The Clinical Research Coordinator will have, or will develop, skills in phlebotomy, electrocardiograms, collection of medical/surgical histories, basic laboratory tests, performance of subject trial visits, completion of case report forms (CRFs), and resolution of data queries. The Clinical Research Coordinator will participate in the completion of regulatory documents. The Clinical Research Coordinator shall have the highest moral and ethical standards and will be expected to conduct themselves in a responsible, professional, moral, and ethical manner at all times. The Clinical Research Coordinator shall have excellent interpersonal communication skills and have a strong commitment to the success of the research team.
Clinical Research Coordinator Responsibilities:
- Assist in the coordination and execution of clinical drug trials under the guidance and direction of the site administrator, principal investigator, and sub-investigators.
- Read, comprehend, and execute clinical trial protocols.
- Perform laboratory tests as required by trial protocol.
- Monitor clinical and laboratory data for accuracy and compliance with trial protocols.
- Complete all documentation required by trial protocol for submission to the trial sponsor.
- Comply with all international, federal, state, local, and company guidance, laws, regulations, policies, and procedures as applicable to clinical research trials and Advanced Research Institute.
- Interact with patients by explaining trial protocols, consenting subjects, monitoring their compliance with protocols, collecting data, and collection laboratory samples.
- Protect every subject's safety to the best of your ability.
- Maintain every patient's rights to privacy.
- Maintain flexibility by performing all other assigned duties.
Training: On the job training. Formal continuing education opportunities provided.
Experience Requirements: Experience is highly preferred but not necessarily required.
Education Requirements: High school diploma required.
Keywords: MA, CNA, Phlebotomist, Research Assistant, Medical Scribe
Job Type: Full-time
Pay: $20.00 - $28.00 per hour
Benefits:
- 401(k) matching
- Dental insurance
- Health insurance
- Paid time off
Experience:
- Clinical research: 1 year (Preferred)
Ability to Commute:
- Sandy, UT 84092 (Required)
Work Location: In person
See All 22 Clinical Research Associate Jobs in Utah
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Find JobsClinical Research Associate Jobs by City in Utah
Where Utah roles are concentrated, by current openings.
Clinical Research Associate 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 associate jobs across Utah.
- Bachelor's degree in life sciences, nursing, pharmacy, or a related clinical field
- Relevant certification such as ACRP's CCRC or CCRP credential preferred by most Utah employers
- Minimum one to two years of clinical trial monitoring or site coordination experience
- Thorough knowledge of ICH-GCP guidelines and FDA regulatory requirements
- Proficiency with electronic data capture systems such as Medidata Rave or Oracle Clinical
- Strong written communication skills for protocol deviation reporting and regulatory submissions
Clinical Research Associate Jobs in Utah: Frequently Asked Questions
How do you become a clinical research associate in Utah?
Start with a bachelor's degree in a life sciences field such as biology, nursing, or pharmacy, which is the baseline expectation for most Utah employers. Utah does not require a state-issued license specific to clinical research associates, so national credentials from the Association of Clinical Research Professionals, such as the CCRC or CCRP, carry the most weight in local hiring. Entry-level candidates often begin in clinical research coordinator roles at hospitals or contract research organizations before moving into monitoring positions.
Which companies hire clinical research associates in Utah?
Employers hiring clinical research associates in Utah right now include University of Utah, Advanced Research Institute, and Care Access, based on current listings on Migrate Mate as of November 2026. Utah's expanding life sciences industry means both contract research organizations and academic medical centers are active year-round sources of openings for this role.
Which Utah cities have the most clinical research associate jobs?
Salt Lake City, Ogden, and Sandy lead for clinical research associate openings in Utah. Salt Lake City anchors the market because of the University of Utah Health system and a dense cluster of pharmaceutical and biotech companies along the Wasatch Front, while Provo and Ogden benefit from nearby research institutions and medical device manufacturers that run ongoing clinical programs.
Are there remote clinical research associate jobs in Utah?
Yes, and more than many clinical roles, because a meaningful portion of the work involves remote data review, sponsor communication, and regulatory documentation rather than on-site patient contact. About 11% of clinical research associate openings tied to Utah are remote or hybrid as of November 2026, reflecting how sponsors and contract research organizations increasingly allow off-site monitoring for routine visits. On-site presence is still required for initiation and close-out visits at Utah trial sites.
How can I get hired as a clinical research associate in Utah with little or no experience?
The most realistic entry path is starting as a clinical research coordinator at a Utah hospital or academic medical center, where you gain direct protocol and regulatory experience. University of Utah Health and Intermountain Health both run research programs that regularly bring on coordinators without prior monitoring experience. Earning your CCRC credential through the Association of Clinical Research Professionals and completing GCP training gives you a concrete edge when applying to coordinator roles that lead directly into associate-level monitoring positions.
Where can I find and apply to clinical research associate jobs in Utah?
You can find and apply to clinical research associate jobs in Utah on Migrate Mate, which lists current Utah openings. Search the available roles, find the ones that match your experience and location, and apply directly to the positions that fit.
See All 22 Clinical Research Associate Jobs in Utah
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