<ul><li>Coordinate and manage clinical trials as per study protocols and regulatory guidelines.</li><li>Screen, recruit, and enroll eligible study participants.</li><li>Obtain informed consent from participants and ensure ethical compliance.</li><li>Collect, record, and maintain accurate clinical data and study documentation.</li><li>Assist investigators during study visits, procedures, and assessments.</li><li>Monitor participant progress, report adverse events, and ensure safety.</li><li>Manage study supplies, kits, and ensure protocol adherence at all times.</li></ul>

Clinical Research Coordinator