Clinical Research Professional with experience on tool Veeva Vault in operations & Information System. 2. Experienced in ensuring the clinical trial documentation in consistent with TMF Master index, study specific expected document list, submission and inspection readiness criteria and comply with SOP and other requirements.Perform Approval and Rejection of Review/Approval workflow via Client’s Document management system according to SOP’s Guidelines. Maintains full understanding of… Show more Clinical Research Professional with experience on tool Veeva Vault in operations & Information System. 2. Experienced in ensuring the clinical trial documentation in consistent with TMF Master index, study specific expected document list, submission and inspection readiness criteria and comply with SOP and other requirements.Perform Approval and Rejection of Review/Approval workflow via Client’s Document management system according to SOP’s Guidelines. Maintains full understanding of documentation properties in order to perform proper execution of controlled documentation activities. Track and follow up on document discrepancies. Communicates document, system, and Hardware issues to support team. Escalate unresolved issues appropriately to TCS team lead and Client support team. Perform quality checks according to Client’s procedures (SOP’s) Communicate/Support/Resolve client issues or queries. Other duties as assigned. Show less