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Institutional Review Board Coordinator Jobs (NOW HIRING)

Institutional Review Board Coordinator The Institutional Review Board Coordinator supports the administrative review, tracking, documentation, and communication of human research submissions. The ...

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Institutional Review Board Coordinator information

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$42.5K

$73.4K

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How much do institutional review board coordinator jobs pay per year?

As of Sep 6, 2026, the average yearly pay for institutional review board coordinator in the United States is $73,375.00, according to ZipRecruiter salary data. Most workers in this role earn between $55,000.00 and $81,500.00 per year, depending on experience, location, and employer.

What is an Institutional Review Board Coordinator?

Institutional Review Board (IRB) Coordinators are professionals who manage and oversee the ethical review process for research involving human subjects. They ensure that research proposals comply with federal regulations, institutional policies, and ethical standards designed to protect participants. IRB Coordinators facilitate communication between researchers and the IRB, organize meetings, review submissions, and maintain documentation. Their work is crucial for safeguarding the rights and welfare of research participants and supporting compliance in academic and clinical research settings.

What are the key skills and qualifications needed to thrive as an Institutional Review Board Coordinator?

To thrive as an Institutional Review Board (IRB) Coordinator, you need a solid understanding of research ethics, regulatory compliance, and human subjects protection, often backed by a bachelor’s degree in a related field. Familiarity with IRB management software, federal compliance systems (such as IRBNet or iRIS), and certifications like Certified IRB Professional (CIP) are commonly required. Strong organizational skills, attention to detail, and effective communication are vital soft skills for managing submissions and liaising with researchers and board members. These skills ensure ethical research practices, regulatory adherence, and efficient review processes crucial to protecting human subjects and institutional integrity.

What are some common challenges Institutional Review Board Coordinators face when managing protocol submissions?

Institutional Review Board Coordinators often encounter challenges such as ensuring timely review of protocol submissions, maintaining compliance with evolving regulations, and communicating effectively with researchers to clarify application requirements. Balancing the administrative workload, tracking multiple projects simultaneously, and addressing incomplete or inconsistent documentation are frequent aspects of the role. Successful coordinators develop strong organizational skills and foster collaborative relationships with IRB members and research teams to streamline processes and uphold ethical standards.

What is the difference between Institutional Review Board Coordinator vs Research Compliance Specialist?

AspectInstitutional Review Board CoordinatorResearch Compliance Specialist
CredentialsTypically requires a bachelor's degree in health sciences, research, or related field; certifications like CCRC may be preferredRequires similar degrees; certifications such as CCRC or IRB-related training are common
Work EnvironmentWorks within research institutions, hospitals, or universities overseeing IRB processesWorks in research institutions or regulatory agencies ensuring compliance across research activities
Employer & Industry UsageCommonly employed by academic institutions, hospitals, and research organizationsFound in research institutions, biotech companies, and regulatory bodies

The Institutional Review Board Coordinator primarily manages IRB submissions and ensures ethical compliance for research studies. In contrast, the Research Compliance Specialist oversees broader research regulations and compliance issues. Both roles require similar credentials and work in research environments, but their focus areas differ slightly, with the IRB Coordinator concentrating on ethical review processes and the Compliance Specialist on overall regulatory adherence.

How much does an Institutional Review Board Coordinator make?

An Institutional Review Board Coordinator typically earns between $50,000 and $70,000 annually, depending on experience, education, and location. The role often requires knowledge of research ethics, regulatory compliance, and documentation management tools.

How to become an Institutional Review Board Coordinator?

To become an Institutional Review Board (IRB) Coordinator, candidates typically need a bachelor's degree in health sciences, research, or a related field, along with experience in research compliance or ethics. Certification such as the Certified IRB Professional (CIP) can enhance job prospects, and strong organizational and communication skills are essential for managing IRB processes and documentation.

What does an Institutional Review Board Coordinator do?

An Institutional Review Board (IRB) Coordinator manages the administrative aspects of the IRB process, including preparing and maintaining documentation, coordinating meetings, and ensuring compliance with federal regulations for research involving human subjects. They often communicate with researchers, review protocols for ethical considerations, and may assist with training and record-keeping to support the IRB's oversight functions.
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Infographic showing various Institutional Review Board Coordinator job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $73,375 per year, or $35.3 per hour.

Institutional Review Board Coordinator

TriHealth, Inc.

Cincinnati, OH • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 7 days ago


TriHealth rating

7.5

Company rating: 7.5 out of 10

Based on 176 frontline employees who took The Breakroom Quiz

231st of 898 rated healthcare providers


Job description

Advance Research. Protect Patients. Make an Impact.

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, investigators, and regulatory leaders to coordinate IRB reviews, ensure adherence to federal regulations, and help protect the rights and welfare of research participants. If you're detail-oriented, organized, and passionate about advancing healthcare through research, we'd love to hear from you.

Why TriHealth. Support meaningful research that improves patient care Collaborate with physicians, investigators, and healthcare leaders Make a direct impact on research compliance and human subject protections Grow your expertise in regulatory affairs and research administration Location: Good Samaritan Hospital at 375 Dixmyth Avenue, Cincinnati, OH 45220 Work Hours: 80 hours biweekly Day shift No Weekends or Holidays commitment Incentives & Benefits: We offer competitive shift differentials, opportunities for professional growth, and a comprehensive benefits package that may include medical, dental, vision, paid time off, retirement savings plans, and tuition reimbursement. Job Requirements: Bachelor's degree required.

3-4 years of experience in clinical research, IRB administration, research compliance, healthcare administration, or a related field. Strong knowledge of medical terminology. Proficient in Microsoft Office Suite, including Word and Excel.

Strong internet research and document management skills. Typing speed of 55-60 WPM preferred. Excellent organizational, communication, and attention-to-detail skills.

Job Overview: This position is an administrative body established to protect the rights and welfare of human research subjects recruited to participate in research activities conducted under the auspices of the institution with which it is affiliated. Responsible for receiving all IRB applications, assuring they meet relevant requirements, and for directly communicating IRB questions and decisions with principal investigator. Working with IRB chair, the IRB Coordinator will also be responsible for communicating with IRB members, sharing documents and establishing and updating the process for IRB renewal and action and standard operating procedure.

Sets logistics for IRB meetings and is responsible for the creation and filing of meeting minutes, as well as communicating with PI the IRB relevant resolution on behalf of the IRB chair. The IRB coordinator has a significant role in assuring that the TriHealth regulatory documents, resolution and communications are continuously and adequately filed. Works in collaboration with peers and the Chairman of the TriHealth IRB to receive, review for completeness, and distribute all paperwork involved with human research studies and maintain all required records and reports of the IRB for TriHealth, including external studies involving recruitment of TriHealth patients, in order to maximize the success of human subject research at TriHealth, and to meet the Food and Drug Administration and Office for Human Subject Protections regulations governing IRB's.

Job Responsibilities: Responsible for coordinating and reviewing all protocol applications submitted to the TriHealth Human Research Protection Program. Provides guidance to faculty and staff for completing the application forms. Communicates frequently with principal investigators to keep apprised of their research application and contractual submission plans.

Acts- as necessary- as a liaison between principal investigator and the IRB. Provides advice on non-technical proposal content and format and providing preliminary reviews of draft proposals or portions of draft proposals. Reviews proposals for accuracy, consistency, and compliance with TriHealth and IRB policy and procedures.

Oversees the maintenance of accurate records of IRB actions by reviewing and suggesting modifications in IRB agendas and minutes prepared by the IRB Coordinator. Periodically reviews IRB policies and procedures with the IRB Chairman and the Vice President of Academic Affairs to ensure appropriate functioning of the IRB. Ensures that investigators and sponsors are informed of actions and findings by the IRB by reviewing IRB SOPs on a regular basis to ensure accurate information and dissemination of changes to investigators and research staff.

Ensures that submitted research is reviewed efficiently and consistent with federal regulation. Reviews the financial and conflict of interests on behalf of TriHealth. Assigns new protocols to the IRB for review after preliminary review has examined impact on TriHealth.

Educates Investigators, Staff, Residents on the IRB's standard operating procedures, appropriate reporting procedures, IRB documents etc. The IRB Coordinator performs the following additional functions, as needed, in support of Institutional Review Board operations: Leads special projects as assigned by the IRB chair, helps with billing to for IRB services, supports and assists with supervision of the IRB secretary Working Conditions: Climbing - Rarely Hearing: Conversation - Consistently Hearing: Other Sounds - Frequently Kneeling - Occasionally Lifting 50+ Lbs. - Rarely Lifting <50 Lbs.

- Occasionally Pulling - Rarely Pushing - Occasionally Reaching - Rarely Sitting - Consistently Standing - Rarely Stooping - Occasionally Talking - Consistently Use of Hands - Consistently Color Vision - Occasionally Visual Acuity: Far - Frequently Visual Acuity: Near - Consistently Walking - Frequently TriHealth SERVE Standards and ALWAYS Behaviors At TriHealth, we believe there is no responsibility more important than to SERVE our patients, our communities, and our fellow team members. To achieve our vision and mission, ALL TriHealth team members are expected to demonstrate and live the following: Serve: ALWAYS... Welcome everyone by making eye contact, greeting with a smile, and saying "hello" Acknowledge when patients/guests are lost and escort them to their destination or find someone who can assist Refrain from using cell phones for personal reasons in public spaces or patient care areas Excel: ALWAYS..

Recognize and take personal responsibility to address and recover from service breakdowns when a customer's expectations have not been met Offer patients and guests priority when waiting (lines, elevators) Work on improving quality, safety, and service Respect: ALWAYS... Respect cultural and spiritual differences and honor individual preferences. Respect everyone's opinion and contribution, regardless of title/role

Speak positively about my team members and other departments in front of patients and guests. Value: ALWAYS... Value the time of others by striving to be on time, prepared and actively participating

Pick up trash, ensuring the physical environment is clean and safe. Be a good steward of our resources, using supplies and equipment efficiently and effectively, and will look for ways to avoid waste. Engage: ALWAYS..

Acknowledge wins and frequently thank team members and others for contributions. Show courtesy and compassion with customers, team members and the community. Apply Apply (Existing Employee).


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About TriHealth

Sourced by ZipRecruiter

TriHealth provides unique opportunities from across disciplines in many different aspects including patient care, care coordination, education and management. We are unique because we know that team members who focus on our mission and values provide excellent patient care.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Cincinnati, OH, US

Year founded

1995