Yaile De La Torre is a dedicated Clinical Research Coordinator with experience in the clinical research industry since 2022. She has played a key role in the successful execution of clinical trials across multiple therapeutic areas, ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.

As a Clinical Research Coordinator, Ms. De La Torre is responsible for coordinating participant visits, managing informed consent procedures, maintaining regulatory documentation, supporting study startup activities, scheduling assessments, and ensuring accurate source documentation and data collection. She also assists with participant recruitment, retention efforts, investigational product accountability, sponsor communications, and monitoring visit preparation.

Her experience includes maintaining regulatory binders, tracking protocol deviations, supporting adverse event reporting, coordinating laboratory procedures, and ensuring compliance with sponsor, IRB, and FDA requirements throughout the conduct of clinical trials.

Ms. De La Torre is committed to providing exceptional participant support while contributing to the delivery of high-quality clinical research, regulatory compliance, and data integrity. Her attention to detail, organizational skills, and dedication to patient care make her a valuable member of the MedHealth Research Solutions team.