A company is looking for a Regulatory Coordinator for Thoracic Oncology.
Key Responsibilities
Manage compliance and documentation for clinical trials, including IRB submissions and regulatory filings
Coordinate study start-up activities and maintain communication with key stakeholders
Prepare and maintain regulatory files and tracking databases to ensure audit readiness
Required Qualifications
Bachelor's Degree or 1 year of relevant experience as an Associate Regulatory Coordinator
0-1 years of experience in a medical or scientific research setting preferred
Fundamental knowledge of clinical trial conduct preferred
Understanding of regulatory guidelines and the IRB submission process
Proficiency in Microsoft applications and databases
Regulatory Coordinator • Lawrenceville, Georgia, United States