<ul><li>Conduct site selection, initiation, monitoring, and close-out visits at clinical trial sites.</li><li>Ensure clinical trials are conducted according to the approved protocol, Good Clinical Practice (GCP), and applicable regulations.</li><li>Monitor patient safety and adherence to ethical guidelines during trials.</li><li>Verify accuracy, completeness, and consistency of data collected in case report forms (CRFs).</li><li>Review and resolve discrepancies in trial data.</li><li>Maintain essential trial documents in compliance with regulatory standards.</li><li>Train site staff on trial protocols, procedures, and regulatory requirements.</li><li>Act as the main point of contact for site personnel, addressing any queries or issues.</li><li>Ensure sites maintain proper trial-related documentation and comply with trial timelines.</li></ul>

Clinical Research Associate