Ref #: 23888

Employment type: Permanent - Full-Time

Location: Mexico - Home/Office Based in Mexico City; Av. Barranca del Muerto region

Posted: 09-Sep-2020

Description

• Ensure consistent receipt, analysis, classification, registration and filing/retrieval of electronic clinical trial essential and non-essential documents and other clinical trial related documents to allow for
their consistent tracking, inspection and security
• Indexing of documents in eTMF Veeva Vault with the required metadata
• Perform peer review and ensure that the document is in final state
• Send rejection information using Microsoft form and notify sender via email
• Run Inactivation/reclassification reports and complete tasks as needed
• Coordinate communications regarding progress and completion of study documentation, package creation and data entry activities to the various functional areas as appropriate
• Run and analyze reports
• Maintain weekly document processing metrics/errors/returns/delays for department - excel spreadsheet

This position will be temporarily home based due to COVID and then it will be a mix of home/office based.