Dedicated Clinical Research Associate with two years of hands-on experience in monitoring clinical trials and ensuring adherence to regulatory standards and study protocols. Proficient in conducting site evaluations, implementing risk-based monitoring, overseeing patient safety procedures, and managing adverse events. Demonstrated ability to conduct monitoring visits, verify data accuracy, and maintain comprehensive documentation. Skilled in collaborating with investigative sites, sponsors, and regulatory authorities to troubleshoot issues and ensure compliance. Strong understanding of GCP guidelines, EDC and IWRS systems. Committed to delivering high-quality research outcomes while upholding ethical standards and patient welfare.