IRB Program Manager

Job Summary

Overseeing the development and evaluation of clinical research trials, the full-time IRB Program Manager will ensure compliance with IRB policies and federal regulations while providing guidance to investigators and coordinating the review of research proposals in a telecommuting environment.

Key responsibilities

• Coordinates review and approvals of research proposals to ensure compliance with IRB and regulatory requirements
• Interacts with governmental agencies regarding research regulations and participates in audits as necessary
• Plans and implements training programs for IRB members and research staff to ensure understanding of applicable laws and requirements

Required qualifications

• Master's degree in a relevant field or equivalent experience
• Experience in clinical research and knowledge of IRB processes and regulations
• Familiarity with FDA and OHRP regulations regarding human subjects research
• Proven ability to manage multiple projects and meet deadlines
• Previous supervisory or mentorship experience in a research setting