Duties & Responsibilities
Management of IRB Protocols:
Performs regulatory review and analysis of research applications submitted to OPRS/IRB for consistency, completeness, and compliance with federal and state regulations and OPRS/IRB policies and procedures.
Solves routine issues within the framework of federal regulations, laws and guidance to human subjects protection and OPRS/IRB policies and procedures.
Determines the appropriate level of review for IRB research submissions and will be designated to conduct exempt and expedited reviews.
Interprets and provides comprehensive guidance to principal investigators, research, and support staff on complex human subjects/research regulations. Ensures the conduct of high-quality human subject research.
Maintains a current understanding of Federal, State, and University laws, regulations and guidelines governing human subject research; attends educational and professional seminars as required to stay current in areas related to human subject research compliance.
Communication and Outreach
Provides guidance and consultation to investigators regarding the interpretation of the Code of Federal Regulations (CFRs), HIPAA and FERPA laws, and NIH and NSF policies, pertaining to human subjects research.
Advises the research community about human subjects protection issues, submission of application materials, review requirements, and institutional policies.
Perform other duties as assigned.