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Weekend Irb Jobs in Tennessee (NOW HIRING)

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Weekend Irb information

What is the difference between Weekend IRB vs IRB Coordinator?

AspectWeekend IRBIRB Coordinator
CertificationsOften requires IRB-related training, but not always formal certificationsTypically requires IRB or research compliance certifications
Work EnvironmentPart-time, flexible hours, often on weekends or eveningsFull-time, office-based, regular weekday schedule
Employer & IndustryResearch institutions, hospitals, universitiesResearch institutions, hospitals, universities

Weekend IRB roles focus on providing oversight during non-standard hours, often with flexible schedules, while IRB Coordinators handle ongoing compliance, documentation, and communication during regular hours. Both roles are essential in research oversight but differ mainly in work hours and specific responsibilities.

What is a weekend IRB?

Weekend IRB jobs refer to positions related to Institutional Review Boards (IRBs) that operate or require work during weekends. IRBs are committees established to review and approve research involving human subjects, ensuring ethical standards are met. Weekend IRB staff may include coordinators, administrators, or reviewers who process submissions, review protocols, and ensure compliance outside of normal weekday hours to accommodate researchers' needs and deadlines.

What are the typical responsibilities of a weekend IRB member?

As a Weekend IRB (Institutional Review Board) member, your primary responsibility is to review research protocols submitted for ethical and regulatory compliance, particularly those requiring urgent or expedited consideration over weekends. This role often involves collaborating remotely with fellow board members, principal investigators, and compliance staff to ensure timely feedback on submissions. Challenges may include balancing multiple protocols with tight deadlines and maintaining clear communication despite limited in-person interaction. Your input directly impacts participant safety and institutional compliance, making attention to detail and ethical judgment essential.

What are the key skills and qualifications needed to thrive as a weekend IRB member?

To thrive as an IRB member, you generally need a background in research ethics, regulatory compliance, and relevant academic or clinical experience, often supported by advanced degrees in health, law, or social sciences. Familiarity with federal regulations (such as 45 CFR 46), online protocol management systems, and human subjects protection certifications (e.g., CITI Program) is typically required. Strong analytical thinking, attention to detail, impartiality, and effective communication skills distinguish outstanding IRB members. These skills ensure that research protocols are ethically reviewed, participant rights are protected, and institutional compliance is maintained.
What are the most commonly searched types of Irb jobs in Tennessee? The most popular types of Irb jobs in Tennessee are:

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

Ballad Health

Kingsport, TN • On-site

Full-time

Re-posted 16 days ago


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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