Hamlyn Williams are working on an exciting role with a client who require an a senior medical writer for a 6 month contract with a view to extend. This role can be offered as a fully remote post. This is a for a Rare Disease focused company.

Duties/responsibilities:

• 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 s.banks@hamlynwilliams.com or for more information please call +1(347) 242 5722.