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Irb Jobs in Ohio (NOW HIRING)

Ohio State University

IRB Protocol Analyst

Columbus, OH · On-site +1

$21.35 - $27.88/hr

IRB Protocol Analyst Department:ERIK | Office of Responsible Research Practices Position Overview The IRB Protocol Analyst supports the review and oversight of human subjects research to ensure ...

TriHealth

Institutional Review Board Coordinator

Cincinnati, OH · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Join TriHealth as an Institutional Review Board (IRB) Coordinator and play a key role in supporting ethical, compliant human research. In this collaborative position, you'll partner with physicians ...

Nationwide Children's Hospital

Coordinates submissions of human subjects research project to the Institutional Review Board (IRB) andof Investigational New Drug Applications (IND's) to the U.S. Food and Drug Administration (FDA)

TriHealth, Inc.

Clinical Research Coordinator

Cincinnati, OH · On-site

$23.25 - $31/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Complies with all IRB/FDA requirements in study submission. Assures compliance with IRB/FDA standards and deadlines in notification of subject randomization and enrollment. Assures compliance with ...

TriHealth

Clinical Research Coordinator

Cincinnati, OH · On-site

$23.25 - $31/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Complies with all IRB/FDA requirements in study submission. Assures compliance with IRB/FDA standards and deadlines in notification of subject randomization and enrollment. Assures compliance with ...

TriHealth

Clinical Research Nurse

Cincinnati, OH · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Comply with all IRB/FDA requirements in study submissions. * Assures compliance with IRB/FDA standards and deadlines in notification of subject randomization and enrollment. * Assures compliance with ...

TriHealth

Clinical Research Nurse

Cincinnati, OH · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Comply with all IRB/FDA requirements in study submissions. Assures compliance with IRB/FDA standards and deadlines in notification of subject randomization and enrollment. Assures compliance with IRB ...

TriHealth, Inc.

Clinical Research Nurse

Cincinnati, OH · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Comply with all IRB/FDA requirements in study submissions. * Assures compliance with IRB/FDA standards and deadlines in notification of subject randomization and enrollment. * Assures compliance with ...

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All JobsIrb JobsIrb Jobs in Ohio

Irb information

See Ohio salary details

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How much do irb jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for irb in Ohio is $35.12, according to ZipRecruiter salary data. Most workers in this role earn between $21.97 and $45.71 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 Ohio?

The most popular types of Irb jobs in Ohio are:

What are popular job titles related to Irb jobs in Ohio?

For Irb jobs in Ohio, the most frequently searched job titles are:

What job categories do people searching Irb jobs in Ohio look for?

The top searched job categories for Irb jobs in Ohio are:

What cities in Ohio are hiring for Irb jobs?

Cities in Ohio with the most Irb job openings:

Irb jobs near you
Infographic showing various Irb job openings in Ohio as of August 2026, with employment types broken down into 86% Full Time, 10% Part Time, and 4% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $73,058 per year, or $35.1 per hour.

IRB Protocol Analyst

Ohio State University

Columbus, OH • On-site, Remote

$21.35 - $27.88/hr

Full-time

Posted 18 days ago

Job description

Screen reader users may encounter difficulty with this site. For assistance with applying, please contact hr-accessibleapplication@osu.edu. If you have questions while submitting an application, please review these frequently asked questions.

Current Employees and Students:

If you are currently employed or enrolled as a student at The Ohio State University, please log in to Workday to use the internal application process.

Welcome to The Ohio State University's career site. We invite you to apply to positions of interest. In order to ensure your application is complete, you must complete the following:

  • Ensure you have all necessary documents available when starting the application process. You can review the additional job description section on postings for documents that may be required.

  • Prior to submitting your application, please review and update (if necessary) the information in your candidate profile as it will transfer to your application.

Job Title:IRB Protocol AnalystDepartment:ERIK | Office of Responsible Research Practices

Position Overview

The IRB Protocol Analyst supports the review and oversight of human subjects research to ensure compliance with federal regulations, state laws, institutional policies, and sponsor requirements. This role partners with investigators, research teams, and Institutional Review Board (IRB) members to facilitate efficient protocol review, regulatory compliance, and timely study approvals.

Key Responsibilities

  • Review and analyze human research submissions of limited scope and complexity.
  • Apply federal regulations, state laws, and institutional policies to support compliant research activities.
  • Provide guidance to investigators and research teams throughout the IRB review process.
  • Document regulatory findings, IRB deliberations, and board actions.
  • Coordinate IRB activities and collaborate with ancillary review committees and institutional partners.
  • Assist researchers in obtaining timely IRB approvals and maintaining ongoing compliance.
  • Prepare regulatory documents, inter-institutional agreements, and materials for institutional signature.
  • Track review timelines and approval deadlines to prevent delays and lapses in compliance.
  • Maintain high-quality standards for regulatory review and documentation.
  • Support customer service initiatives and respond to investigator inquiries.
  • Contribute to process improvement projects and educational program development.
  • Assist with training and outreach for research teams and IRB members.
  • Manage communications and documentation within the electronic IRB submission system.

What You'll Bring

  • Strong attention to detail and organizational skills.
  • Ability to interpret and apply regulatory requirements and policies.
  • Effective communication and customer service skills.
  • Commitment to supporting ethical, compliant, and efficient human subjects research.

Required Qualifications

  • Bachelor's degree or an equivalent combination of education and experience.
  • Customer service experience.
  • Problem-solving experience.
  • Ability to work in a regulatory and deadline driven environment.
  • Ability to work almost exclusively on a computer using regulatory application software.
  • Proficient use of Microsoft Office Suite.
  • Strong written and verbal communication skills.

Desired Qualifications

  • Knowledge and/or experience with research methods, IRB operations, regulations and policies governing the protection of human subjects in research.

Application Materials

  • A resume and cover letter are strongly desired.
Additional Information:

Salary

The pay range for this job profile is $21.35 - $27.88 per hour. The offer for this position will fall within this range based on multiple factors including internal equity, unit's available budget, and the candidate's qualifications.

Additional Information

There are 4 positions are available with this search

Ohio State will not sponsor applicants for a work visa for this position.

Work Location

Employees are provided several flexible work schedule and location options aligned with U.S. Eastern Time Zone including an option for remote. All employees are provided university-configured equipment and supportive technology tools. Employees are required to provide reliable internet access and home office furnishings for approved remote work locations.

This position will start as a hybrid role, working at least 3 days per week in office for the first 6 weeks.

ERIK Overview

Join the Enterprise for Research, Innovation and Knowledge (ERIK) at The Ohio State University and become a part of a dynamic, forward-thinking team dedicated to pushing the boundaries of discovery and innovation. ERIK positions Ohio State to expand curiosity-driven research and creative expression, further develop our research community of faculty, staff, and students, and grow the innovation ecosystem to address big challenges and improve communities locally and globally. We are seeking passionate individuals who are committed to making a meaningful impact through collaboration, innovation, and excellence. To learn more about our mission and work, please visit https://erik.osu.edu/.

Position Mapping

  • Function: Research Administration

  • Sub function: Research Protocol

  • Career Band and Level: S1

Location:Mount Hall (0311)Position Type:RegularScheduled Hours:40Shift:First Shift

Final candidates are subject to successful completion of a background check. A drug screen or physical may be required during the post offer process.

Thank you for your interest in positions at The Ohio State University and Wexner Medical Center. Once you have applied, the most updated information on the status of your application can be found by visiting the Candidate Home section of this site. Please view your submitted applications by logging in and reviewing your status. For answers to additional questions please review the frequently asked questions.

The university is an equal opportunity employer, including veterans and disability.

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