Regulatory Compliance Officer

Job Summary

Ensuring compliance with research protocols, the full-time Regulatory Compliance Officer will manage the regulatory aspects of clinical trials remotely, including protocol reviews, submission of documents, and communication with research sponsors.

Key responsibilities

• Collaborates with investigators to confirm regulatory safeguards in study development
• Conducts detailed 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 field
• At least 1 year of experience in a research or administrative capacity related to research projects
• Knowledge of research regulations, guidelines, and compliance issues
• Experience in developing informed consent documents and preparing regulatory submissions
• Familiarity with IRB processes and federal or industry sponsor requirements