● Responsible for initial indexing and review of study documentation for Trial Master File●(TMF) quality for sponsor and/or CRO studies●As in project rooms and ensure they are completed within timeline Keep study specific trackers up-to-date and communicate them to the leads Attend weekly/biweekly meetings with the PMs/clients and discuss project issues andstatus● Coordinate with Clinical Document Leads for project related queries OnCheck documents in… Show more ● Responsible for initial indexing and review of study documentation for Trial Master File●(TMF) quality for sponsor and/or CRO studies●As in project rooms and ensure they are completed within timeline Keep study specific trackers up-to-date and communicate them to the leads Attend weekly/biweekly meetings with the PMs/clients and discuss project issues andstatus● Coordinate with Clinical Document Leads for project related queries OnCheck documents in clarification and rejection status for assigned projects• ●Review reports for clarification and rejection monthly before the reports are sent out to the client.●Keep project mappings up-to-date, coordinate with the study leads for requirement of changes to mappings.●Perform internal reviews of assigned eTMFS for audit readiness.● Review internal audit reports and perform corrective actions as required Assist with User Acceptance Testing during product development and release●Work on cross functional teams including Project Management, Business Development; P Client Services, Development, and IT on the implementation and management of client projects. Show less