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Irb Jobs in Tennessee (NOW HIRING)

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Irb information

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$12

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How much do irb jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for irb in Tennessee is $38.78, according to ZipRecruiter salary data. Most workers in this role earn between $24.26 and $50.47 per hour, depending on experience, location, and employer.

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 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.

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 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.

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 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 most commonly searched types of Irb jobs in Tennessee?

The most popular types of Irb jobs in Tennessee are:

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

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

What cities in Tennessee are hiring for Irb jobs?

Cities in Tennessee with the most Irb job openings:

Infographic showing various Irb job openings in Tennessee as of August 2026, with employment types broken down into 83% Full Time, 16% Part Time, and 1% Contract. Highlights an 84% Physical, 4% Hybrid, and 12% Remote job distribution, with an average salary of $80,669 per year, or $38.8 per hour.

Institutional Review Board Assistant (8a-5p) Research Institute - Kingsport, TN

Ballad Health

Kingsport, TN • On-site

Full-time

Re-posted 26 days ago


Ballad Health rating

6.5

Company rating: 6.5 out of 10

Based on 228 frontline employees who took The Breakroom Quiz

605th of 887 rated healthcare providers


Job description

Job Description:
Summary:
The Institutional Review Board Assistant will be responsible for co-managing the daily administrative activities of the Ballad Health Institutional Review Board (IRB) office. The Assistant shall provide consultation and instruction to individuals within the community. This individual will process all submissions to the IRB. This includes new applications, continuing renewals, amendments, SAEs, and other adverse event reports. The Assistant shall review claims of exemptions and expedited reviews as assigned, as well as to ensure all submissions meet the federal and state guidelines, as well as Ballad Health policies. The Assistant will manage protocol review information. The Assistant will designate the type of IRB board review required for each submission. This individual will assign scientifically appropriate submissions to the appropriate IRB board meeting agendas for review and create and maintain board meeting agendas. The Assistant shall maintain meeting minutes, IRB rosters, hard copies, electronic files, and all other required regulatory documents in compliance with federal regulations, institutional policies, and IRB SOPs. Additionally, the Assistant will initiate trials once the Principal Investigator has all IRB approval letters and stamped documentation through written correspondence to investigators of all IRB actions and decisions. The Assistant will manage and process all applications through IRBNet. This individual will answer questions related to submissions, FDA compliance, and general research education submitted by all investigators and research staff. The Assistant shall ensure research staff training and credentials are complete and accurate with each study submission. The Assistant will act as local administrator for IRBNet: maintain the local system and be a resource for local issues and maintain current IRB study files within a 10-year timeframe.
The Assistant will ensure that all Federal regulations are being followed and maintained. The Assistant will be knowledgeable of Code of Federal Regulations, Good Clinical Practice Guidelines, Common Rule, and basic research method. The Assistant shall be responsible for any additional duties as assigned.
Requirements:
Associates Degree preferred. Applicant must have organizational skills, ability to make deadlines,superior communication skills and be service oriented.
Work Requirements:
Shift: Day
On Call: No
Weekends: No
Travel Required: No Travel
Shift Details: 8a-5p
City/State: Kingsport, TN
Location:

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About Ballad Health

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Become a part of the Ballad Health story. Together, we are transforming our region. We're making communities healthier. We're expanding access to critical services in rural areas.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Johnson City, TN, US