Dadahayath Shaik

Biography

 I am a Post graduate in Biotechnology with more than 10 years of hardcore experience in the field of clinical research with thorough understanding and knowledge about clinical operations, Site operations, Patient recruitment, pharmacovigilance, Project management, Document Management( e-TMF) , Quality assurance methods, Business analyst,Drug supply chain management( IVRS & IWRS User acceptance testing ( UAT), Scenarios and scripts for UAT) and regulatory process in India, SEA region.  • Attend investigator meetings as required Create training test scenarios/Test scripts for IVRS/IWRS/EDC and approve tests • Conducting pre-UAT meeting with the client, creating data and test scripts on basis of the template for testing purpose. • Involved in Planning, Management and Conduct of UAT activities of Rave (EDC) studies. Also serves as a primary QC personnel for UAT.

Research Interest

  Clinical Trials, GCP, ICH-GCP