IRB Program Manager

Job Summary

Overseeing the development and compliance of clinical research trials, the full-time IRB Program Manager will manage IRB procedures, provide regulatory guidance, and ensure adherence to federal and state regulations while working remotely.

Key responsibilities

• Coordinates review and approvals of research proposals to ensure compliance with IRB policies and regulations
• Interacts with governmental agencies and prepares for audits related to research regulations
• Plans and implements training programs for physicians and IRB members on regulatory guidelines and compliance

Required qualifications

• Master's degree in a relevant field or equivalent experience in clinical research administration
• Experience with IRB processes and federal regulations governing human subject research
• Strong understanding of ethical considerations in clinical research
• Proven ability to develop and implement training programs
• Experience in managing audits and interactions with regulatory agencies