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Clinical Research Associate Jobs in Utah (NOW HIRING)

Numinus

Clinical Research Coordinator II

Draper, UT · On-site

$22.75 - $30.25/hr

At Cedar Clinical Research...Healing Happens Here! Join our team and play an integral role in helping individuals achieve mental wellness. Numinus/Cedar Clinical Research has an esteemed team of ...

University of Utah

Research Associate

Salt Lake City, UT · On-site

$90K - $120K/yr

Details Open Date 05/18/2026 Requisition Number PRN45009B Job Title Research Associate Working Title Leadership Development and Systems Improvement Specialist Career Progression Track A00 Track Level ...

Imh

$19.50 - $26.48/hr

The purpose of this position is to assist in duties and activities associated with supporting clinical research and research studies at Intermountain Healthcare. A key responsibility of this position ...

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How much do clinical research associate jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for clinical research associate in Utah is $37.44, according to ZipRecruiter salary data. Most workers in this role earn between $26.25 and $47.93 per hour, depending on experience, location, and employer.

Is it hard to get a clinical research associate job?

Securing a clinical research associate (CRA) position can be competitive, often requiring a relevant degree such as a life sciences or healthcare-related field, along with experience in clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and familiarity with clinical trial management systems can improve job prospects, but entry may be challenging for those without relevant qualifications or experience.

What is a clinical research associate?

Clinical Research Associates (CRAs) are professionals responsible for monitoring and overseeing clinical trials to ensure they are conducted in accordance with regulatory guidelines, protocols, and ethical standards. They play a key role in ensuring the safety of trial participants and the integrity of collected data. CRAs often visit clinical trial sites to verify data accuracy, maintain study documentation, and provide training to site staff. Their work ensures that new drugs, treatments, or medical devices are tested rigorously before they reach the market.

What are the key skills and qualifications needed to thrive as a clinical research associate?

To thrive as a Clinical Research Associate, you need a solid background in life sciences, attention to detail, and experience with clinical trial protocols, often supported by a relevant bachelor's degree. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and sometimes certifications like ACRP or SOCRA is typically required. Strong organizational, communication, and problem-solving skills help build effective relationships with research sites and ensure compliance. These skills are vital for maintaining the integrity of clinical trials, ensuring regulatory adherence, and advancing medical research efficiently.

What is the difference between Clinical Research Associate vs Clinical Trial Coordinator?

AspectClinical Research AssociateClinical Trial Coordinator
CredentialsBachelor's degree, often with clinical research certificationsBachelor's degree, often with clinical research or healthcare certifications
Work EnvironmentMonitors clinical sites, reviews data, ensures complianceCoordinates trial activities, manages schedules, and communicates with sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, research institutions, CROs

Both roles are essential in clinical trials, with CRAs focusing on site monitoring and compliance, while Clinical Trial Coordinators handle day-to-day trial management. They often collaborate but have distinct responsibilities within the clinical research process.

Is being a clinical research associate worth it?

A clinical research associate (CRA) monitors clinical trials to ensure compliance with protocols and regulations, often requiring strong organizational and communication skills. The role offers opportunities for career growth, competitive salaries, and the chance to contribute to medical advancements, but it can involve irregular hours and travel. Overall, it can be a rewarding career for those interested in healthcare and research.

What are some common challenges clinical research associates face when monitoring clinical trial sites?

Clinical Research Associates (CRAs) often encounter challenges such as ensuring protocol compliance across multiple sites, managing tight project timelines, and maintaining accurate documentation. Additionally, CRAs must effectively communicate with site staff to resolve issues and ensure data integrity, all while adhering to regulatory guidelines. Balancing frequent travel, adapting to different site environments, and handling unexpected issues such as patient recruitment delays are also typical aspects of the role.
More about Clinical Research Associate jobs
What are the most commonly searched types of Clinical Research jobs in Utah? The most popular types of Clinical Research jobs in Utah are:
What are popular job titles related to Clinical Research Associate jobs in Utah? For Clinical Research Associate jobs in Utah, the most frequently searched job titles are:
What job categories do people searching Clinical Research Associate jobs in Utah look for? The top searched job categories for Clinical Research Associate jobs in Utah are:
What cities in Utah are hiring for Clinical Research Associate jobs? Cities in Utah with the most Clinical Research Associate job openings:
Clinical Research Associate jobs near you
Infographic showing various Clinical Research Associate job openings in Utah as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $77,875 per year, or $37.4 per hour.

Clinical Research Coordinator II

Numinus

Draper, UT • On-site

$22.75 - $30.25/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 24 days ago

Job description

At Cedar Clinical Research...Healing Happens Here! Join our team and play an integral role in helping individuals achieve mental wellness. Numinus/Cedar Clinical Research has an esteemed team of medical professionals dedicated to the clinical research in the use of psychedelic-assisted psychotherapy. This research is changing the future of how we treat mental illnesses. It's pretty exciting here and we'd love for you to join our team!
We value diversity and strive to create an inclusive work environment. We respect and celebrate individuals for their differences and encourage applicants from all backgrounds to apply.
We are looking for someone who is highly motivated, organized, and able to work independently to join our team. This Clinical Research Coordinator II position will be in our Draper Clinic. (in-person not remote)
Responsibilities:
  • Coordinating and performing responsibilities related to research participants including pre-screening, scheduling, overseeing patient visits, and obtaining informed consent
  • Preparing, submitting, and maintaining IRB regulatory documents
  • Ensuring quality data and compliance to the protocol
  • Entering data into EDC systems
  • Conducting ECG's
  • Performing blood draws
  • Packaging and shipping labs
  • Ordering Lab and Study supplies
  • Obtaining medical history/medical records
  • Documenting, reporting, and tracking AE's and SAE's
  • Preparing for site visits or audits from sponsors and/or other agencies in conjunction with Regulatory Specialist

Qualifications:
  • 3 years experience as a Clinical Research Coordinator
  • Must have High School Diploma or GED, Bachelor's Degree preferred
  • Phlebotomist Experience

Benefits:
  • 401(k) matching
  • Medical, Dental, Vision, & Life insurance
  • Flexible spending account
  • Paid time off

Schedule:
  • Day shift (Hours dependent on Randomization Days)
  • Salaried Position (min. 40 hours per week)
  • Monday to Friday

Requirements
Education:
  • High school or equivalent (Required)

Experience:
  • Clinical Research Coordinator: 3 years (Required)

License/Certification:
  • Phlebotomy Certification (Preferred)

Apply