about 1 year ago
Hamlyn Williams are working on an exciting role with a client who require a contract medical writer for a 6 month project with a view to extend. This role can be offered as a fully remote post.
This is an excellenty opportunity work for a fast paced biotech who are looking to rapidly grow over the next year and have multiple opportunities across the business.
- Prepares complex clinical documents that present clinical data objectively and in a clear, concise format. This includes, but may not be limited to: protocols and amendments, Clinical Study Reports (CSRs), Investigator Brochures (IBs), briefing books, response to authorities, etc.
- Preparing Regulatory documents for FDA submissions
- Operates within the Global Regulatory department
- Candidates will be expected to work independently.
- Work to best practices.
This client is actively considering applications ready for interview so please send your CV to email@example.com or for more information please call +1(347) 242 5722.