Experienced Clinical Research Associate (CRA) with over four years of expertise in regulatory and monitoring activities within the pharmaceutical and healthcare research industry. Proficient in ICH-GCP guidelines and UK clinical trial regulations. Adept at coordinating with regulatory authorities, ethics committees, and cross-functional teams. Proven ability to ensure compliance, manage documentation, and support site staff through audits, inspections, and submissions. Currently pursuing an M.A. in Public Health at Nottingham Trent University and seeking a freelance part-time opportunity to leverage my regulatory experience in a dynamic clinical research environment.