IRB Regulatory Coordinator, Remote, Baptist Jacksonville
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AI Summary
Coordinates day-to-day IRB operations to ensure compliance with federal regulations and ethical standards for human subject research. Facilitates regulatory review processes and supports committee operations while maintaining electronic IRB systems.
About Baptist Health
Recognized as a top place to work in health care, Baptist Health cares for more patients in Northeast Florida than any other provider, ranking as “most preferred” for more than 30 years. We’re Jacksonville's only locally governed, faith-based, not-for-profit health system and provide a full spectrum of preventive and specialty care through 200+ locations and six hospitals. Our centers of excellence include Baptist MD Anderson Cancer Center, Baptist Heart Hospital, Baptist Neurological Institute and Wolfson Children's Hospital.
IRB Regulatory Coordinator, Remote, Baptist Jacksonville
The IRB Regulatory Coordinator supports the day-to-day operations of the Institutional Review Board (IRB) by coordinating regulatory, administrative, and operational activities that ensure compliance with federal regulations, institutional policies, and ethical standards governing human subject research. This position serves as a key resource for investigators, research staff, and IRB members by facilitating regulatory review processes, supporting committee operations, maintaining electronic IRB systems, and promoting continuous quality improvement across the research enterprise.
The IRB Regulatory Coordinator partners with Research Administration, Compliance, investigators, and hospital leadership to support efficient IRB operations while safeguarding the rights and welfare of research participants.
Approved Remote States:
Alabama
Florida
Georgia
Idaho
Indiana
Kentucky
Louisiana
Mississippi
North Carolina
Oklahoma
South Carolina
South Dakota
Tennessee
Texas
West Virginia
Wyoming
Education Required:
Associate of Arts or Associate of Science degree.
Bachelor's degree in Business Administration, Health Administration, or a related field preferred.
Experience Required:
Minimum one (1) year of experience with federal regulations governing human subjects research and their application in an IRB environment.
Minimum one (1) year of experience supporting or coordinating IRB or research compliance processes.
Minimum one (1) year of experience utilizing electronic IRB systems and regulatory documentation practices.
Primary Location:
Remote - FloridaAutomatically Apply to the Best Remote Jobs
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