Regulatory Compliance Officer - Ohio

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
• Maintains tracking systems for protocol reviews and communicates updates to relevant parties

Required Qualifications

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