The Clinical Research Compliance Assistant Specialist will work closely with the Research Compliance team to help manage the SUNY Upstate Medical University Human Subject Protection Program, which is inclusive of the IRB and IBC, in accordance with University policies, regulatory standards, ethical principles, and best practices.
Assists with reviews of submissions to the IRB and IBC, provide guidance and a formal written review to the principal investigator and study team via the IRB submission system. Primary responsibility will be administrative review and oversight of the IRB reliance submissions for an external IRB throughout the study lifecycle. Ensures IRB and IBC requirements, stipulations and changes are completed. Assists in providing education and consultation to Upstate research community related to submission requirements and the conduct of the research. Assists the Research Compliance team in developing and deploying new forms, templates, instructions and educational programs. Supports the efforts within Research Compliance related to the development and deployment of an education training program.