-Responsible for the management of designated clinical trials, entering the data into the Electronic Data Capture Database from Electronic Medical Records.-Ensure the conduct of the trial is in compliance with the currently approved protocol/amendment.-To significantly improve quality assurance and consistency in Electronic Data capturing and data.-To Resolve the Queries raised about entered data in Electronic Data Capture Database by on-site team.

-ClinSoft Clinical Data Management System Practice-eTMF Practice-Practice on ICH GCP, Indian GCP, FDA and ICMR guidelines-CTRI registration-Reading Clinical research protocol and making documents such as:Informed Consent FormCase Report FormAccountability logInventory logSafety ReportingDrug compliance Essential DocumentsInformed Consent ProcessPatient's Visits Source DocumentEssential Documents and TMF Preparation

Working under molecular Biology department, performing Molecular test RT-PCR and Genome sequencing of the Covid, Tuberculosis etc.

Worked in Microbiology and Molecular biology department. Done Microbiology Tests such as Anti-biotic susceptibility and Molecular biology RT PCR tests of Covid, TB, HLA B27, Dengue, H1N1,etc.Maintained Test and patients related documents for ICMR audits and followed GLP

Worked as Molecular technician performing RT PCR test of Covid.