Senior IRB Coordinator

Job Summary

Independently applying knowledge of OHRP/FDA regulations, the full-time Senior IRB Coordinator will coordinate the review and approval of IRB submissions, oversee board meetings, and provide regulatory support to investigators while working remotely.

Key responsibilities

• Coordinate review and approvals of research submissions to ensure compliance with federal, state, and local requirements
• Oversee Board meetings, including assigning reviews, maintaining quorum, and providing regulatory guidance
• Act as a liaison between the IRB and the research community, providing guidance on FDA/OHRP regulations and responding to inquiries

Required qualifications

• Bachelor's degree in a relevant field; advanced degree preferred
• Extensive knowledge of OHRP/FDA regulations related to human subject research
• Experience in coordinating IRB submissions and conducting regulatory reviews
• Proven ability to oversee meetings and manage compliance-related tasks
• Strong presentation skills for educational initiatives and training