GT Medical Technologies, Inc.

• Conduct site monitoring visits, including site feasibility, initiation, routine monitoring, and close-out visits, in accordance with SOP, protocol requirements, GCP and applicable regulatory requirements. • Deliver protocol-specific and study-related training to assigned sites and maintain consistent communication to address study expectations, questions, and emerging issues. • Perform source data review and verification to ensure accuracy and completeness of clinical trial data. • Assess site compliance with the protocol, GCP, and applicable regulations by reviewing study conduct, documentation practices, and data quality; escalate significant findings when necessary. • Monitor overall study progress at assigned sites by reviewing enrollment activity, CRF completion, EDC entry, and query resolution. • Escalate site compliance issues, protocol deviations, and data quality concerns to the CRM/Senior CRM as appropriate. • Verify that essential regulatory documents are collected and filed appropriately in the Trial Master File (TMF) and confirm that the Investigator Site File (ISF) is maintained in accordance with GCP and local regulatory standards. • Document monitoring activities and site interactions through timely visit reports, follow-up correspondence, and action plans to ensure resolution of findings. • Collaborate with cross-functional study team members to support effective study execution and issue resolution. • Contribute to the development and implementation of site-level recruitment plans when applicable. • Conduct site close-out visits and ensure resolution of outstanding data queries, regulatory reconciliation, and completion of required site close-out activities. • Provide support during site start-up activities as needed. • Support regulatory document management activities, including tracking, and filing of required study documentation.