<ul><li>Online monitoring of studies to ensure that studies are conducted in accordance with GCP, SOPs, Protocol &amp; regulatory guidelines.</li><li>Review 100% of clinical raw data for completeness, accuracy, and for compliance with the study protocol, GCP, SOPs and applicable regulatory guidelines.</li><li>Review of tabulat listing appended to report and scan check of individual subject CRF as per clinical raw data, sponsor and regulatory requirements.</li><li>Issuance, reconciliation and accountability of forms.</li><li>Preparation of projects for QA Audit and archiving.</li><li>Review of applicable SOPs.</li></ul>

Officer / Sr. Officer - QA / QC ( Clinic )