

Detail- oriented clinical research coordinator with experience in subject recruitment, informed consent, protocol compliance, and data documentation, aiming to support successful clinical trials while ensuring regulatory and ethical standards.
Experienced in coordinating clinical trial activities, ensuring compliance with study protocols, ICH-GCP guidelines, and regulatory requirements. Successfully managed subject enrollment and retention through effective scheduling and follow-up procedures, while maintaining essential documentation such as investigator site files and regulatory binders. Collaborated with principal investigators, sub-investigators, and sponsors to facilitate seamless trial execution and timely resolution of data queries. Demonstrated proficiency in adverse event reporting and audit readiness, contributing to high standards of data quality and regulatory compliance.