IRB Coordinator: Ethical Research and Compliance Lead

TriHealth

Cincinnati, Northern (OH, KY)

Hybrid

USD 55,000 - 90,000

Full time

3 days ago
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Benefits offered by this job

Medical, dental, vision benefits
Paid time off
Tuition reimbursement
Retirement savings plan

Job summary

TriHealth seeks an Institutional Review Board (IRB) Coordinator to support ethical, compliant human research. You will coordinate IRB reviews, liaise with physicians, investigators, and regulatory leaders, and ensure adherence to federal regulations to protect participants.

This administrative role partners with the IRB chair, manages meeting logistics, prepares minutes, and maintains regulatory documents to support TriHealth research activities.

Qualifications

  • Bachelor's degree required.
  • 3-4 years of experience in clinical research, IRB administration, or related field.
  • Proficient in Microsoft Office Suite and strong document management skills.

Responsibilities

  • Coordinate and review all protocol applications submitted to the TriHealth IRB and provide guidance to investigators.
  • Communicate with principal investigators to stay informed of submission plans and serve as liaison between PI and the IRB.
  • Review proposals for accuracy, compliance with TriHealth and IRB policies, and maintain records of IRB actions.
  • Manage IRB meeting logistics and file meeting minutes; update SOPs as needed.
  • Educate Investigators on IRB procedures and support special projects as assigned.

Skills

Medical terminology
Strong communication
Attention to detail
Typing speed 55-60 WPM
Project coordination

Education

Bachelor's degree

Tools

Microsoft Office Suite

Job description

TriHealth seeks an Institutional Review Board (IRB) Coordinator to support ethical, compliant human research. You will coordinate IRB reviews, liaise with physicians, investigators, and regulatory leaders, and ensure adherence to federal regulations to protect participants.

This administrative role partners with the IRB chair, manages meeting logistics, prepares minutes, and maintains regulatory documents to support TriHealth research activities.

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