The Role
The Senior Medical Writer - Regulatory/Clinical will be responsible for researching, creating and editing all documents associated with clinical research.
1. Writing Clinical Study Reports, Protocols, Informed Consent to Clinical Overviews etc
2. Managing multiple projects
3. Reviewing all documentation to a high standard
You
To apply for this role as a Senior Medical Writer - Regulatory/Clinical, our client is hoping for someone with the following skills and experience;
4. 2 years' experience within a CRO Medical writing position
5. Good stakeholder management
6. Can work independently
7. Degree educated in life sciences