As a Clinical Document Specialist you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
This role focuses on quality control of regulatory submission documents and is dedicated to global pharma company
Works in the global team to provide number and technical quality control (QC) to CSP, CSR and submission documents, and ensures the supporting documents are filed for inspection or audit
Works in the global team to compile CSR appendices, and coordinates the CSR publishing
Uses project management skills to track and to timely complete the assigned tasks
Supports the technical platform of MW, including but not limited to the support of document management system (Veeva), document review/comment system, maintaining the related templates, EndNote libraries and related SharePoint sites
Achieve high quality results with the assigned tasks with little or no supervision
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