South Carolina Regulatory Coordinator

Serving as the Regulatory Coordinator for the Clinical Trial Research Program in Pulmonary, Critical Care, Gastroenterology, Endocrinology, Nephrology, and Hepatology, the full-time position will manage study-specific regulatory processes, ensure compliance with regulations and SOPs, and coordinate with Clinical Research Coordinators and the Program Manager, all while working remotely. Key responsibilities Coordinate study start-up activities, including document submission and regulatory compliance Maintain regulatory documentation and oversee electronic regulatory binders for multi-site projects Create and manage eSource documentation databases throughout the study lifecycle Required qualifications Bachelor's degree One year of relevant program experience Familiarity with regulatory processes and documentation for clinical trials Experience with electronic data management systems Knowledge of IRB and safety reporting requirements