Research Regulatory Manager

Job Summary

To support clinical research initiatives, the full-time salaried Research Regulatory Manager will develop training for researchers, ensure compliance with regulatory requirements, and oversee the IRB submission process while working remotely.

Key responsibilities

• Develop and present training related to research processes and procedures to stakeholders
• Audit the informed consent process and assist in preparing for study monitoring visits
• Oversee the IRB submission process and supervise Research Regulatory Coordinators

Required qualifications

• Bachelor's degree (required)
• Experience in clinical research and human subjects' protection regulations, including HIPAA authorizations and IRB process (required)
• 5 years of experience in research administration (preferred)
• Professional certification such as CCRP, CHRC, or ACRP-CP (preferred)