Isabel C. Restrepo, CRC

Clinical Research Coordinator

Isabel C. Restrepo is an experienced Clinical Research Coordinator with a strong background in clinical trial operations and research site management. Since 2019, she has been actively involved in the coordination and execution of clinical studies across multiple therapeutic areas, ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.

Ms. Restrepo has extensive experience managing participant visits, informed consent procedures, regulatory documentation, source documentation, data collection, participant recruitment, retention strategies, and study startup activities. She plays a critical role in maintaining protocol compliance, preparing for monitoring visits, supporting adverse event reporting, and coordinating communication between sponsors, CROs, investigators, and study participants.

In addition to her coordinator responsibilities, Ms. Restrepo has valuable experience in clinical trial budget management, contract review and negotiation support, feasibility assessments, and direct sponsor interactions. Her operational knowledge allows her to effectively support both the financial and clinical aspects of study execution while fostering strong relationships with sponsors and research partners.

Known for her organizational skills, attention to detail, and commitment to quality, Ms. Restrepo contributes significantly to the successful conduct of clinical trials and the delivery of high-quality research outcomes at MedHealth Research Solutions.