Permanent fully home-based working considered
The Medical Writer/Senior Medical Writer will be part of a global Medical Writing group and will work closely alongside team of Medical Writers in the UK.
Reporting into the Medical Writing Manager, you will be responsible for.
Creating and editing all clinical research documents including Clinical Study Reports, Safety Narratives and Protocols
Perform literature searches and reviews
Act as a key point of contact for clients for medical writing projects
Project management acting as a key representative on project teams and attending/leading project team meetings as required
The successful candidate will:
Be able to demonstrate 3-5 years of experience editing and writing clinical documents within a CRO or pharma environment
Hold strong IT skills including Microsoft Word, Excel, Powerpoint and SharePoint
Have previously mentored junior Medical Writers
Hold a Bachelors degree (or equivalent qualification) in a relevant Life Sciences/Scientific subject
To apply, please contact Natalie Robson at CPL Life Sciences via email on firstname.lastname@example.org and please attach an updated version of your CV.
We look forward to hearing from you soon
- Agency: Clinical Professionals
- Contact: Natalie Robson
- Reference: JO-2011-457572
- Posted: 12th November 2020
- Expires: 10th December 2020