Senior Regulatory Documentation Scientist
5 days ago
CK Group are recruiting for a Senior Regulatory Documentation Scientist to join a pharmaceutical company with a site based in Welwyn on a contract basis for 6 to 12 months
**The Role**:
The main purpose of the role will be to
- Manage the preparation of regulatory documents, such as Clinical Dossiers and suite of Safety Documents
- Review documents to ensure compliance with documentation quality standards, regulatory requirements and consistency of messages across all documents for a product and within a clinical dossier
- Prepare specifications for outsourced work, including writing/review of documents, and serve as liaison for projects
**Your Background**:
To succeed in this role, you will come from a Life science background and previous writing experience, specifically authoring and/or editing regulatory documentation
- Project management as well as an ability to independently evaluate and blend data from a broad range of disciplines
**Apply**:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference 54288 in all correspondence.
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