1

Biotechnology Research Associate Jobs in Utah (NOW HIRING)

CRA 1, IQVIA Biotech

Pleasant View, UT · On-site

$71K - $145K/yr

IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring. Must have ... Job Overview The Clinical Research Associate I (CRA I) plays a key role in supporting the ...

IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring. Must have ... Job Overview The Clinical Research Associate I (CRA I) plays a key role in supporting the ...

IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring. Must have ... Job Overview The Clinical Research Associate I (CRA I) plays a key role in supporting the ...

IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring. Must have ... Job Overview The Clinical Research Associate I (CRA I) plays a key role in supporting the ...

Manufacturing Associate

Logan, UT · On-site

$15 - $18.40/hr

The job opportunity is for one of our clients specializing in biotechnology product development ... research, safety, and education. As the global leader in serving the field of science, our client ...

next page

Showing results 1-20

Biotechnology Research Associate information

See Utah salary details

$14

$29

$42

How much do biotechnology research associate jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for biotechnology 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 does a biotechnology research associate do?

A Biotechnology Research Associate supports scientific research projects in the field of biotechnology. Their responsibilities typically include conducting experiments, analyzing data, maintaining laboratory equipment, and preparing reports or presentations about research findings. They often work under the supervision of senior scientists and collaborate with other research staff. This role is essential in both academic and industry settings, as it helps drive innovation in areas such as medicine, agriculture, and environmental science.

What opportunities for professional growth and advancement are available to biotechnology research associates?

Biotechnology Research Associates often have opportunities to advance by taking on more complex research projects, specializing in niche areas such as genomics or cell culture, or pursuing supervisory roles. Many organizations encourage continued education and may support attendance at conferences or workshops to stay current with emerging technologies. Collaborating closely with senior scientists and cross-functional teams also helps expand skill sets and build valuable professional networks, opening pathways to roles such as Research Scientist or Project Manager.

What is the difference between Biotechnology Research Associate vs Laboratory Technician?

AspectBiotechnology Research AssociateLaboratory Technician
Required CredentialsBachelor’s or Master’s in Biology, Biotechnology, or related fieldAssociate degree or certification in laboratory sciences
Work EnvironmentResearch labs, biotech companies, academic institutionsClinical, industrial, or research laboratories
Employer & Industry UsageUsed in biotech research, pharmaceutical development, academiaCommon in clinical labs, manufacturing, quality control

The Biotechnology Research Associate typically holds a higher degree and engages in experimental design and data analysis, whereas Laboratory Technicians focus on routine testing and sample preparation. Both roles are essential in biotech and lab settings, but the Research Associate often takes on more complex research tasks.

What skills and qualifications are needed to be a biotechnology research associate?

To thrive as a Biotechnology Research Associate, you need a solid background in molecular biology, biochemistry, or related fields, usually supported by a bachelor's or master's degree. Familiarity with laboratory equipment, data analysis software, and techniques such as PCR, gel electrophoresis, and cell culture is typically required. Strong attention to detail, critical thinking, and effective teamwork are essential soft skills in this role. These skills and qualities are crucial for producing reliable research results, ensuring safety and compliance, and contributing meaningfully to scientific advancements.
What are popular job titles related to Biotechnology Research Associate jobs in Utah? For Biotechnology Research Associate jobs in Utah, the most frequently searched job titles are:
What job categories do people searching Biotechnology Research Associate jobs in Utah look for? The top searched job categories for Biotechnology Research Associate jobs in Utah are:
What cities in Utah are hiring for Biotechnology Research Associate jobs? Cities in Utah with the most Biotechnology Research Associate job openings:
Infographic showing various Biotechnology Research Associate job openings in Utah as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 27% Part Time, 1% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $61,619 per year, or $29.6 per hour.

CRA 1, IQVIA Biotech

IQVIA

Pleasant View, UT • On-site

$71K - $145K/yr

Full-time

Re-posted 23 days ago


IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

62nd of 223 rated it services


Job description

IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring. Must have experience monitoring in oncology solid tumor.

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.

Job Overview

The Clinical Research Associate I (CRA I) plays a key role in supporting the successful conduct of clinical research studies by performing site monitoring and site management activities. In this position, you will ensure that assigned study sites conduct trials in compliance with the protocol, applicable regulations, Good Clinical Practice (GCP), and ICH guidelines. This role is essential in protecting patient safety, ensuring highquality clinical data, and maintaining study integrity.

Key Responsibilities

As a CRA I, you will conduct various types of monitoring visits-including site selection, initiation, routine monitoring, and closeout visits-to evaluate the quality and integrity of site practices. You will verify that study activities are performed according to regulatory requirements and sponsor expectations, escalating quality concerns as necessary. During these visits, you will review essential documents, assess protocol adherence, oversee data entry and query resolution, and ensure maintenance of both the Trial Master File (TMF) and the Investigator Site File (ISF).

A central part of this role involves building and maintaining strong communication with investigative sites. You will provide protocol training, set expectations, address sitelevel challenges, and support recruitment planning to help sites meet enrollment targets. You will also collaborate closely with internal project teams to ensure cohesive study execution and may contribute to site-level financial processes or startup activities based on study needs.

Accurate and timely documentation is critical. The CRA I prepare detailed monitoring visit reports, followup letters, and all required study documentation to ensure audit readiness and transparent oversight. The ability to manage multiple tasks, prioritize effectively, and work independently while maintaining productive team relationships is essential for success.

Qualifications

  • Bachelor's degree required; a scientific or healthcare discipline is preferred.
  • 6 months -2 years of relevant experience, with equivalent combinations of education, training, or completion of a CRA training program considered.
  • Basic knowledge of clinical research regulations (GCP/ICH).
  • Ability to travel as required by the project.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $71,900.00 - $145,300.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

What IQVIA employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


IQVIA logo

About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US