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Senior Clinical Research Associate Jobs in Utah (NOW HIRING)

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Contract Senior CRA

Salt Lake City, UT · Remote

As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing ... for a Senior Clinical Research Associate. * In-depth knowledge of clinical trial processes ...

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CRA II and Senior CRA

Salt Lake City, UT · Remote

We are currently seeking a Clinical Research Associate (Level II or Senior) to join our diverse and dynamic team. As a CRA II/Senior CRA at ICON, you will play a pivotal role in designing and ...

University of Utah

Research Associate

Salt Lake City, UT · On-site

$70K - $130K/yr

The Senior Research Associate will lead and contribute to projects (e.g., instrument development, intervention evaluations, professional learning design, and policy-relevant research) that directly ...

University of Utah

Research Associate

Salt Lake City, UT · On-site

$70K - $130K/yr

The Senior Research Associate will lead and contribute to projects (e.g., instrument development, intervention evaluations, professional learning design, and policy-relevant research) that directly ...

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Senior Clinical Research Associate information

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$32.8K

$85.9K

$130.6K

How much do senior clinical research associate jobs pay per year?

As of May 28, 2026, the average yearly pay for senior clinical research associate in Utah is $85,861.00, according to ZipRecruiter salary data. Most workers in this role earn between $56,900.00 and $116,500.00 per year, depending on experience, location, and employer.

What Does a Senior Clinical Research Associate Do?

A senior clinical research associate (CRA) monitors clinical trials and manages team members. Your duties include leading project team meetings, running experiments, making observations, tracking results, and analyzing data. You also ensure experiments meet all clinical practice and safety standards. Qualifications for this career are a bachelor of science in a biomedical field or a bachelor of science in nursing (BSN), along with professional experience in a medical or research setting. You must have strong communication, interpersonal, leadership, and technical writing skills.

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

To thrive as a Senior Clinical Research Associate, you need a solid background in clinical research, regulatory compliance, and often a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and relevant certifications such as ACRP or SOCRA are typically required. Strong organizational skills, attention to detail, and the ability to communicate effectively with diverse stakeholders make someone stand out in this position. These skills and qualities are vital for ensuring studies are conducted ethically, accurately, and in compliance with regulatory standards.

What are some typical challenges faced by Senior Clinical Research Associates when overseeing multiple clinical trials?

Senior Clinical Research Associates (SCRAs) often manage several studies at once, which requires balancing competing deadlines, ensuring protocol compliance, and maintaining strong communication with site staff. A common challenge is ensuring consistent data quality and regulatory adherence across diverse sites, especially when trials are geographically dispersed. Effective time management, attention to detail, and proactive problem-solving are crucial for success in this role. Collaboration with project managers, investigators, and regulatory teams is also essential to ensure trials progress smoothly and meet all regulatory requirements.

What is a Senior Clinical Research Associate?

A Senior Clinical Research Associate (Senior CRA) is an experienced professional responsible for overseeing and monitoring clinical trials to ensure compliance with regulatory requirements, protocols, and good clinical practice. They often serve as a liaison between the sponsor and clinical sites, ensuring data integrity and patient safety. Senior CRAs may also mentor junior staff, manage multiple studies, and resolve complex issues that arise during trials. Their work is critical in bringing new medical treatments and devices to market safely and efficiently.
More about Senior Clinical Research Associate jobs
What are the most commonly searched types of Senior Clinical Research jobs in Utah? The most popular types of Senior Clinical Research jobs in Utah are:
What are popular job titles related to Senior Clinical Research Associate jobs in Utah? For Senior Clinical Research Associate jobs in Utah, the most frequently searched job titles are:
What job categories do people searching Senior Clinical Research Associate jobs in Utah look for? The top searched job categories for Senior Clinical Research Associate jobs in Utah are:
What cities in Utah are hiring for Senior Clinical Research Associate jobs? Cities in Utah with the most Senior Clinical Research Associate job openings:
Senior Clinical Research Associate jobs near you
Infographic showing various Senior Clinical Research Associate job openings in Utah as of May 2026, with employment types broken down into 3% As Needed, 63% Full Time, 32% Part Time, and 2% Contract. Highlights an 93% Physical, 1% Hybrid, and 6% Remote job distribution, with an average salary of $85,861 per year, or $41.3 per hour.
Senior Clinical Research Associate

Senior Clinical Research Associate

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Salt Lake City, UT • Hybrid

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 5 days ago

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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