<ul><li>Assist in planning, coordinating, and executing clinical research studies.</li><li>Collect, review, and maintain accurate clinical trial data and documentation.</li><li>Ensure compliance with regulatory guidelines, protocols, and ethical standards.</li><li>Coordinate with investigators, sites, and vendors for smooth study conduct.</li><li>Monitor patient recruitment and follow-up to meet study timelines.</li><li>Support preparation and submission of regulatory documents and reports.</li><li>Participate in site visits, audits, and inspections as required.</li><li>Maintain effective communication with clinical teams and stakeholders.</li><li>Assist in data entry, validation, and query resolution in clinical databases.</li></ul>

Clinical Research Executive