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Irb Jobs in Utah (NOW HIRING)

University of Utah

PS Clinical Research Coord

Murray, UT · On-site

$59K - $65K/yr

Coordinates with study sponsor, investigator and IRB to complete study closure activities. 9. Complete time budget assessments and designate study charges vs. standard of care on clinical trials. 10. ...

Imh

Work closely with regulatory teams and the IRB, to incorporate guidelines to ensure research programs are fully compliant. * Ensure research employees are adequately supported through training ...

University of Utah

PS Study Coordinator

Salt Lake City, UT · On-site

$31K - $48K/yr

Reports serious AEs to IRB and sponsor. * Documents all protocol deviations, reconciles test article accountability at study close out and prepares summary report for sponsor. * Completes, audits ...

University of Utah

PS Study Coordinator

Salt Lake City, UT · On-site

$45K - $50K/yr

Reports serious AEs to IRB and sponsor. * Documents all protocol deviations, reconciles test article accountability at study close out and prepares summary report for sponsor. * Completes, audits ...

University of Utah

PS Study Coordinator

Salt Lake City, UT · On-site

$31K - $48K/yr

Reports serious AEs to IRB and sponsor. * Documents all protocol deviations, reconciles test article accountability at study close out and prepares summary report for sponsor. * Completes, audits ...

University of Utah

Study Coordinators

Salt Lake City, UT · On-site

$22K - $57K/mo

Reports serious AEs to IRB and sponsor. 10. Document all protocol deviations, reconcile test article accountability at study close out and prepare summary report for sponsor. 11. Complete, audit ...

Utah State University

Program Coordinator I

Logan, UT · On-site

Knowledge of research and information gathering methods, including strict adherence to IRB protocols and research ethics. * Ability to make independent administrative/procedural decisions and ...

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How much do irb jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for irb in Utah is $34.67, according to ZipRecruiter salary data. Most workers in this role earn between $21.69 and $45.11 per hour, depending on experience, location, and employer.

What does an IRB analyst do?

An IRB analyst reviews research protocols to ensure they comply with ethical standards and regulatory requirements. They evaluate risks, consent processes, and study procedures, often working with institutional review boards to approve or modify research proposals. Strong attention to detail and knowledge of federal regulations are essential for this role.

What are the key skills and qualifications needed to thrive as an IRB administrator, and why are they important?

To thrive as an IRB Administrator, you need expertise in research ethics, regulatory compliance, and human subject protection, usually supported by a relevant bachelor's or master's degree. Familiarity with IRB management software, federal regulations (such as the Common Rule), and certifications like CIP (Certified IRB Professional) are typically required. Strong organizational skills, attention to detail, and effective communication are crucial for coordinating reviews and guiding researchers. These skills ensure ethical research practices, regulatory compliance, and the protection of research participants.

What are the typical responsibilities of an IRB coordinator, and how do they interact with researchers and regulatory bodies?

An IRB (Institutional Review Board) coordinator is responsible for managing the review process of research protocols involving human subjects to ensure compliance with ethical standards and federal regulations. This role involves working closely with researchers to guide them through the submission process, reviewing applications for completeness, and facilitating communication between the IRB committee and research teams. Coordinators also serve as liaisons with regulatory bodies, maintain records, and help organize IRB meetings. Strong organizational, communication, and regulatory knowledge are essential, as coordinators often balance multiple projects and deadlines while ensuring research integrity and participant safety.

How to get an IRB job?

To get an IRB (Institutional Review Board) job, candidates typically need a background in research ethics, healthcare, or related fields, along with relevant experience. Certifications such as the CITI Program Human Subjects Research course can be beneficial, and strong knowledge of regulatory requirements like 45 CFR 46 is often required. Positions may require a bachelor's or higher degree and attention to detail in reviewing research protocols.

What is an IRB?

An Institutional Review Board (IRB) is a committee established to review and approve research involving human subjects. The primary purpose of the IRB is to ensure that the rights, welfare, and privacy of participants are protected throughout the research process. IRBs review research proposals to ensure ethical standards are met and that risks to participants are minimized. They are required for most research conducted at universities, hospitals, and other organizations that receive federal funding.

What is the difference between Irb vs Clinical Research Coordinator?

AspectIrbClinical Research Coordinator
Required CredentialsOften requires IRB training, ethics certificationRequires research experience, sometimes certifications
Work EnvironmentReview boards, research institutionsClinical sites, hospitals, research centers
Employer & Industry UsageUsed in research oversight, ethics reviewUsed in managing clinical trials, patient coordination
Common Search & Comparison IntentUnderstanding roles in research ethicsUnderstanding clinical trial management

IRBs (Institutional Review Boards) focus on ethical review and approval of research protocols, ensuring participant safety. Clinical Research Coordinators manage the day-to-day operations of clinical trials, including patient recruitment and data collection. While both roles are integral to clinical research, IRBs oversee ethical compliance, whereas Coordinators handle trial execution.

What are the most commonly searched types of Irb jobs in Utah? The most popular types of Irb jobs in Utah are:
What are popular job titles related to Irb jobs in Utah? For Irb jobs in Utah, the most frequently searched job titles are:
What job categories do people searching Irb jobs in Utah look for? The top searched job categories for Irb jobs in Utah are:
Irb jobs near you
Infographic showing various Irb job openings in Utah as of August 2026, with employment types broken down into 68% Full Time, 21% Part Time, and 11% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $72,108 per year, or $34.7 per hour.

Clinical Research Regulatory Coordinator

IsoTalent

Ogden, UT • On-site

$20 - $25/hr

Other

Medical, Retirement, PTO

This job post has expired today. Applications are no longer accepted.

Job description

CR Regulatory Coordinator

Location: Ogden, UT - Onsite


Our client, a respected clinical research organization, seeks a CR Regulatory Coordinator to join their regulatory affairs team on-site. Do you love keeping complex projects organized and compliant down to the smallest detail? Does the idea of being the go-to person who keeps clinical studies moving smoothly through IRB approvals excite you? If you answered yes, this could be the perfect CR Regulatory Coordinator role for you. Keep scrolling to see what this company has to offer.


The Perks!

  • Compensation: $20.00 - $25.00/hourly, based on experience
  • + quarterly bonuses based on site performance
  • 401k + 3% employer matching
  • Health insurance, employer pays 20% of the employee’s premium
  • Paid Time Off
  • FSA


A Day in the Life of a CR Regulatory Coordinator:

In this role, you'll be the backbone of regulatory compliance for clinical studies, preparing and submitting documentation to the IRB while making sure every study stays aligned with federal and site-specific requirements. You'll work closely with the Principal Investigator and study team, keeping regulatory binders and electronic systems accurate and audit-ready. Your work directly supports the organization's mission by helping studies launch, run, and close out without compliance hiccups.


Responsibilities include:

  • Preparing, facilitating, submitting, and maintaining IRB applications for study start-up, protocol revisions, amendments, administrative changes, and more
  • Completing, auditing, and maintaining study records and databases to ensure compliance with study protocols, FDA, IRB, and site SOPs
  • Preparing regulatory documents and securing signatures for FDA 1572s, Financial Disclosure Forms, Protocol Signature Pages, IB Acknowledgment of Receipts, Delegation Logs, and training documents
  • Filing correspondence and key documents in electronic regulatory systems and paper-based regulatory binders
  • Communicating with research staff, sponsors, and project teams to ensure accuracy of regulatory documents and submissions
  • Tracking study approvals and expirations to prevent lapses in project approval
  • Submitting study renewal applications and progress reports to the IRB
  • Coordinating with sponsors, investigators, and the IRB across the full study lifecycle, from start-up to closure
  • Guiding investigators and research staff on regulatory process and policy questions
  • Recommending and implementing improvements to regulatory processes
  • Staying current on federal and institutional research guidelines


Requirements and Qualifications:

  • 1+ year of clinical research experience
  • Prior experience supporting a Principal Investigator or study team directly
  • Solid experience preparing or submitting regulatory documents (e.g., IRB submissions, FDA 1572s, financial disclosure forms, delegation logs)
  • Experience using Veeva Site Vault or a similar electronic regulatory system
  • CCRP certification preferred
  • Experience handling safety or protocol deviation reporting to an IRB
  • Strong organizational skills and meticulous attention to detail
  • Comfort working with both electronic regulatory systems and paper-based filing
  • A proactive, team-oriented attitude with genuine enthusiasm for supporting clinical research


About the Hiring Company:

Our client is a clinical research organization dedicated to advancing medical knowledge through well-run, participant-focused clinical trials. They value clinical excellence, integrity, and collaboration among their research staff.


Come Join Our Regulatory Affairs Team!

Start by filling out this 3-minute, mobile-friendly application here. We look forward to hearing from you!

Apply