IRB Coordinator II

Responsible for the day to day operations and oversight of the Institutional Review Board. In conjunction with the Chairman, Conduct full IRB reviews (expedited/exempt). Independently manage investigator submissions Assist in SOP development and compliance review Liaison with investigators, sponsors, compliance officers. Support audit readiness, ensures hospital policies and procedures are maintained in compliance with the FDA, code of Federal Regulations, and Good Clinical Practice. Monitors the overall safety of the research patient, including HIPAA. CIP preferred (Certified IRB Professional).

2–4 years IRB or research compliance Education: Bachelor’s required / Master’s preferred-Certifications: Eligibility for CIP preferred (Certified IRB Professional)