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Contract Research Associate Jobs in Utah (NOW HIRING)

Certified Group

Micro Lab Tech

Logan, UT

$16.50 - $21.75/hr

Labstat - A global leader in contract research and testing for nicotine, tobacco, cannabis, hemp ... Associate degree in Life Science or two years of laboratory experience, preferred * Broad knowledge ...

Pharmatech, Inc.

Packout Packaging Associate

Lindon, UT

$13.50 - $16.75/hr

Pharmatech Labs, located in Lindon, Utah, is a premier nutritional contract manufacturer ... Concept development, Research and development, Customization and flavor work, In-house laboratory ...

Pharmatech, Inc.

Packout Packaging Associate

Lindon, UT

$13.50 - $16.75/hr

Pharmatech Labs, located in Lindon, Utah, is a premier nutritional contract manufacturer ... Concept development, Research and development, Customization and flavor work, In-house laboratory ...

Pharmatech, Inc.

Packout Packaging Associate

Lindon, UT · On-site

$13.50 - $16.75/hr

Pharmatech Labs, located in Lindon, Utah, is a premier nutritional contract manufacturer ... Concept development, Research and development, Customization and flavor work, In-house laboratory ...

University of Utah

Program Management

Salt Lake City, UT · On-site

$68K - $78K/yr

... Associate Director, Research & Underserved Medicine Programs Career Progression Track M00 Track ... Oversee purchasing, reimbursements, stipends, contracts, and financial documentation. Coordinate ...

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All JobsContract Research Associate JobsContract Research Associate Jobs in Utah

Contract Research Associate information

See Utah salary details

$14

$29

$42

How much do contract research associate jobs pay per hour?

As of Jun 22, 2026, the average hourly pay for contract research associate in Utah is $29.62, according to ZipRecruiter salary data. Most workers in this role earn between $23.85 and $33.70 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Contract Research Associate, and why are they important?

To thrive as a Contract Research Associate, you need a solid background in life sciences or a related field, attention to detail, and experience with clinical research processes. Familiarity with regulatory systems like FDA guidelines, Good Clinical Practice (GCP), data management tools, and electronic data capture (EDC) systems is typically required. Strong organizational skills, effective communication, and the ability to work independently or in teams help set candidates apart. These competencies ensure that clinical trials are conducted accurately, compliantly, and efficiently, supporting successful research outcomes.

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

AspectContract Research AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like CCRP beneficialBachelor's degree in health sciences or related field; certifications like CCRP or CCRC advantageous
Work EnvironmentTypically in pharmaceutical or biotech companies, contract research organizations (CROs)Usually in hospitals, clinics, or research sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, academic medical centers, research institutions
Common Search & ComparisonYesYes

While both roles support clinical trials, a Contract Research Associate primarily works for pharmaceutical or biotech companies managing trial processes remotely or at sites, often on a contractual basis. A Clinical Research Coordinator typically works directly at research sites, coordinating patient visits and data collection. Both roles require similar credentials and certifications, but their work environments and employer types differ.

What are some typical challenges faced by Contract Research Associates when managing multiple studies simultaneously?

Contract Research Associates often juggle several clinical trials at once, which can pose challenges in time management and prioritization. Balancing the requirements of different sponsors, adhering to varying protocols, and ensuring accurate documentation for each study demand strong organizational skills. Additionally, staying up to date with regulatory changes and effective communication with site staff are crucial to avoid delays and ensure compliance. Developing efficient workflows and leveraging project management tools can help address these challenges.

What is a Contract Research Associate?

A Contract Research Associate (CRA) is a professional who is typically hired on a contractual basis to support and manage clinical trials or research projects. Their primary responsibilities include monitoring research sites, ensuring compliance with protocols and regulations, collecting and verifying data, and maintaining proper documentation. CRAs play a critical role in ensuring the integrity and safety of clinical studies, often working for pharmaceutical companies, contract research organizations (CROs), or academic institutions. The contract nature of the role means that assignments are usually project-based and may vary in duration and scope.
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What cities in Utah are hiring for Contract Research Associate jobs? Cities in Utah with the most Contract Research Associate job openings:
Contract Research Associate jobs near you
Infographic showing various Contract Research Associate job openings in Utah as of June 2026, with employment types broken down into 1% As Needed, 49% Full Time, 48% Part Time, 1% Temporary, and 1% Contract. Highlights an 79% Physical, 3% Hybrid, and 18% Remote job distribution, with an average salary of $61,619 per year, or $29.6 per hour.
Senior Clinical Research Associate

Senior Clinical Research Associate

Icon plc

Salt Lake City, UT • Hybrid

Full-time

Medical, Dental, Vision, Life, Retirement

Posted yesterday

Job description

Contract Senior Clinical Research Associate - Home-Based (US)

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


We are currently seeking a Contract Senior Clinical Research Associate to join our diverse and dynamic team. This will be for a 6 month contract. As a Senior Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

What you will be doing

  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
  • Collaborating with investigators and site staff to facilitate smooth study conduct.
  • Performing data review and resolution of queries to maintain high-quality clinical data.
  • Contributing to the preparation and review of study documentation, including protocols and clinical study reports


Your profile

  • Bachelor's degree in a scientific or health-related field or an equivalent combination of education and clinical research experience, particularly in a study coordinator or nursing role
  • Minimum of 3 years independent monitoring
  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
  • Strong organizational and communication skills, with attention to detail.
  • Ability to work independently and collaboratively in a fast-paced environment.
  • Ability to travel at least 80% of the time (international and domestic - fly and drive) and should possess a valid driver's license

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a requesthere.

Are you a current ICON Employee? Please click here to apply

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