Senior IRB Coordinator

Job Summary

Working remotely full-time, the Senior IRB Coordinator will independently manage the review and approval of IRB submissions, oversee board meetings, and provide regulatory support to investigators and study staff.

Key responsibilities

• Coordinates review and approvals of research submissions to ensure compliance with federal, state, and local regulations
• Independently oversees Board meetings, including assigning reviews and providing regulatory guidance
• Acts as a liaison between the IRB and the research community, offering guidance on FDA/OHRP regulations and IRB submission requirements

Required qualifications

• Extensive knowledge of OHRP/FDA human subject research regulations
• Experience in coordinating IRB submissions and overseeing board meetings
• Ability to provide regulatory and ethical guidance to investigators
• Strong background in quality assurance and compliance within research settings
• Experience in developing and presenting educational initiatives for the research community