Regulatory Associate

Job Summary

A company is looking for a Regulatory Associate in the Department of Surgery.

Key Responsibilities

• Prepare, submit, and maintain essential regulatory documents for clinical trials
• Provide guidance and training to research teams on regulatory compliance and best practices
• Participate in study initiation meetings and serve as a liaison between investigators and regulatory bodies

Required Qualifications

• Bachelor's Degree or equivalent
• 2 years of related experience; education may be considered in lieu of experience
• Thorough understanding of human subjects' research regulations
• Experience in reviewing study protocols and informed consent documents
• Ability to provide technical assistance regarding IRB/IACUC submissions