
Regulatory Compliance Officer
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; collaborates with investigators during study development to facilitate and confirm that appropriate regulatory safeguards have been included; conducts detailed reviews of assigned protocols and informed consent forms prior to IRB review. Develops IRB submission packets for protocols, including writing of abstract, submission of standard forms and drafting of informed consent forms; provides and maintains tracking system to assess progress of a protocol's review. Serves as principal contact from CTO to regulatory agencies including FDA and IRBs.
1 year experience in research or administrative capacity working on research projects
Knowledge of research regulations, guidelines and compliance issues required
Experience developing informed consent documents and preparing regulatory documents desired
Experience and knowledge of IRB and federal or industry sponsor processes and requirements preferred
Time Management
Record Keeping Skills
Compliance reporting skills
Process Improvement
Verbal communication
Detail Oriented
written communication
Adaptability
Multi-tasker
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The Ohio State University is a public research university in Columbus, Ohio. Founded in 1870 as a land-grant university and the ninth university in Ohio with the Morrill Act of 1862, the university was originally known as the Ohio Agricultural and Mechanical College. Ohio State is home to the Wexner Medical Center and world-class graduate and undergraduate programs.

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