Negotiable depending on experience
about 1 year ago
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 oferring 40 hours per week.
This role is due to start immediately.
- Prepare 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 will be a remote role in however candidates will be expected to be in the office when required (1 day a month) so being based in a commutable distance to Central NJ is important.
This client is actively considering applications ready for interview so please send your CV to firstname.lastname@example.org or for more information please call +1(347) 242 5722.