<ul><li>Prepare and review protocols for clinical studies.</li><li>Ensure compliance to protocol, SOPs and Regulatory requirements.</li><li>IEC coordination and communication.</li><li>Handle safety related issues and ensure appropriate communication and to manage and monitor adverse events.</li><li>Prepare and review reports for clinical studies.</li><li>Help maintain and update all the systems and SOPs in the department.</li><li>Training &amp; others.</li></ul>

Principle Investigator / Co-investigator