Ohio Licensed Regulatory Compliance Officer

Job Summary

A company is looking for a Regulatory Compliance Officer for the Clinical Trials Office.

Key Responsibilities

• Collaborates with investigators to ensure regulatory safeguards in study development
• Conducts reviews of protocols and informed consent forms prior to IRB submission
• Acts as the main contact for regulatory agencies and monitors compliance with regulations

Required Qualifications

• Bachelor's Degree in biological sciences, health sciences, social sciences, or a related field
• One year of experience in a research or administrative role related to research projects
• Knowledge of research regulations, guidelines, and compliance issues
• Experience in developing informed consent documents and regulatory submissions is desired
• Familiarity with IRB and federal or industry sponsor processes is preferred