Senior Medical Writer

An excellent opportunity has arisen for a Senior Medical Writer to join an exciting and growing pharmaceutical company based in central London.

Within this role you will be responsible for authoring clinical regulatory documents such as CSRs, IBs and INDs.

Within this role you can either be office based, or fully home based!

Responsibilities:
- Typical projects will involve analysis and reporting of clinical data and information, working on a range of regulatory documents including protocols and amendments, CSRs, IBs, INDs, clinical summaries and overviews, briefing documents, response to authorities, and PIPs.


- As well as authoring more complex document types, we provide opportunities to review and perform quality checks on documents prepared by junior writers, so you will have the chance to pass on your expert skills and knowledge to coach, mentor and train team members.

Skills & Experience:
- Candidates should have a strong academic background in a life science discipline
- Experience in regulatory writing either as a part of pharmaceutical or CRO company, strong written and oral communication skills, commitment to highest quality outputs, high attention to detail, a professional service mentality, and an ability to build rapport and strong relationships with both internal and external colleagues.

For further details, please contact Tim Barratt on +44(0)1727 817 626 or email a copy of your CV to tbarratt@keypeople.co.uk


  • Start: a.s.a.p
  • Rate: £3500 - £55000.00 per annum + excellent bonuses
  • Location: London, England
  • Type: Permanent
  • Industry: Pharmaceutical
  • Recruiter: Key People
  • Tel: +44 (0)1727 817 626
  • Fax: 01727 844 838
  • Email: to view click here
  • Posted: 2019-02-21 16:41:13 -

  • View all Jobs from Key People


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