In this position, you will perform assessment, quality control and publishing of scientific documents to ensure content, format and technical quality are consistent and compliant with internal and external guidelines. Further, you will provide first-line user support for electronic Document Management System and support project leads with system maintenance and roll-out activities. Your accountabilities will include: - Perform source data verification (SDV) and technical quality control (QC) of submission documents - Provide advice when required to authors on SDV requirements, technical formatting processes and the use of document management systems - Compile, integrate and publish applicable documents with word processing, electronic publishing and document management systems
Are you looking to work in a global growth company where you can make a real difference? Then you are right with us!
Global Pharma Company.
If you are interested then kindly send your resume to: firstname.lastname@example.org
- Relevant work experience with electronic document management systems (e.g., Documentum, Veeva Vault etc.) and document review - Basic understanding of non-clinical, clinical and regulatory deliverables relevant to submission dossiers - Demonstrated ability to work successfully within a matrix environment and influence cross functional teams - Flexible and detail-oriented approach to documentation management, as appropriate
Undergraduate degree preferably in a scientific discipline or business vocation
English : Very good