Medical Writer
- Permanent
- Clinical Development, Clinical/Medical Writing
This vacancy has now expired. Please see similar roles below...
Hobson Prior are looking for a Medical Writer to join a rapidly growing Regulatory Affairs team at a Contract Research Organisation in London. This is an exciting opportunity to develop and grow your career where you will accomplish tasks and projects to contribute to the company's success.
Job Responsibilities:
- Responsible to write clinical study reports, protocols, clinical development plans, FDA briefing documents, and IND, NDA, and MAA modules;
- Coordinate quality control reviews of documents and maintaining audit trails of changes;
- Deliver input on data analysis planning and interpretation.
Key Skills:
- Strong computer skills, project management skills, and a high attention to detail; and
- Excellent communication skills (both written and oral).
Requirements:
- Degree in a life science or engineering field (PhD preferred).
- Prior experience in the research, pharmaceutical, or medical device industry preferred.
Apply now:
If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.
Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.
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