<ul><li>To conduct the volunteer screening process for study.</li><li>To participate and supervise the volunteer enrolment process.</li><li>To ensure timeliness and compliance of the study execution with respect to the protocol specifications at all stages of the study.</li><li>To act as a study coordinator in bio studies.</li><li>To assist in protocol, investigator brochure, ICF and CRF preparation.</li><li>To assist during conduct of bio study (drug dispensing supervision and dosing supervision).</li><li>To maintain the study documents.</li><li>To compile the data for Ethics Committee presentation.</li><li>To assist in preparation of clinical study report.</li></ul>

Project Coordinator