Coordinate and schedule subject visits within specific window per protocol guidelines. Assist Coordinator in CTMS management. Prepare visit-specific documentation and charts for Clinical Research Coordinator. Assist Coordinator in monitoring subject flow and assist in subject care and management. Administer all mandatory questionnaires to study subjects. Promptly request all necessary medical records for Serious Adverse Event Reporting. Inform subjects and obtain written re-consents in regard to Informed Consent Forms. Assist Coordinator in regulatory management, including training and monitoring visits.