<ul><li>Protocol, Informed Consent Form (ICF), Case Report Form (CRF) preparation</li><li>Coordinate with the Principal Investigator for submitting the study related documents (clinical updates) to Independent Ethics Committee</li><li>Coordinate with the investigator for planning of study schedule, Ensure the completion of study related documents</li><li>Report Preparation</li><li>Feasibility Assessment</li></ul>

Clinical Investigator