<ul><li>Monitor clinical trials to ensure compliance with protocols, GCP, and regulatory guidelines.</li><li>Conduct site visits to assess trial progress, patient recruitment, and data quality.</li><li>Assist in the selection, initiation, and close-out of clinical trial sites.</li><li>Review case report forms (CRFs), source documents, and ensure accurate data entry.</li><li>Liaise with investigators, site staff, and project teams to resolve queries and issues.</li><li>Track study timelines, milestones, and ensure adherence to project schedules.</li><li>Prepare and maintain essential trial documents, reports, and monitoring visit logs.</li><li>Ensure patient safety and ethical conduct throughout the study.</li></ul>

Clinical Research Associate