The Regulatory Compliance Officer assures that research protocols of the OSUCCC Clinical Trials Office (CTO) are in compliance with University, state and federal regulations; ensures timely submission of all appropriate paperwork for review by appropriate agency.ResponsibilitiesCollaborates with investigators during study development to facilitate and confirm that appropriate regulatory safeguards have been includedConducts detailed reviews of assigned protocols and informed consent forms prior to IRB reviewEnsures timely submission of protocol documents for review by appropriate agency communicates with all CTO research projects sponsors (academic, federal, industry) to ensure complianceInterfaces with various