IRB Specialist II or IRB Specialist III

IRB Specialist II
The Institutional Review Board Specialist II will process and review research protocols involving human subjects and related actions, and obtain required institutional approvals. This position requires excellent communication skills and appropriate application of research administration principles, practices, and procedures.

**IRB Specialist III
**The Institutional Review Board Specialist III will conduct independent initial, expedited, and continuing reviews of complex research studies – including clinical trials and FDA-regulated research. Provide regulatory guidance (such as DHHS and FDA regulations) to evaluate participant risk and informed consent, counseling principal investigators, study coordinators, and students on submission procedures and compliance requirements. Assist in training new OHSP staff or campus researchers and help update internal office procedures and guidelines.