Regulatory Compliance Officer

Job Summary

Ensuring compliance with research protocols, the full-time Regulatory Compliance Officer will facilitate study development, conduct detailed protocol reviews, and manage submissions to regulatory agencies in a remote setting.

Key responsibilities

• Collaborates with investigators to confirm 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 stakeholders

Required qualifications

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