Senior Medical Writer - Regulatory

South East England Permanent £55,000 - £65,000
  • A fantastic opportunity to join a high performing, market leading business
  • The chance to work remotely and to be involved in high profile projects

About Our Client

A progressive, respected and innovative specialist consultancy who work primarily in advanced therapy medicinal products (ATMPs) for a range of Pharma, Biotech and Life Sciences clients

Job Description

  • Preparation of clinical documents including clinical study protocols and reports.
  • Preparation of Investigator brochures
  • Preparation of EU and US regulatory documents (e.g. Common Technical Document clinical summaries and overviews, scientific advice briefing documents, paediatric investigation/study plans, and orphan drug designation applications)
  • Project management of client assignments
  • Scheduling meetings with clients

The Successful Applicant

The successful candidate will have experience of medical writing, ideally within the pharmaceutical industry.

They will have a minimum of a B.Sc. in a life sciences subject.

They will have experience of preparing key regulatory and clinical documents, and will, ideally, have experience of writing PIPs, Orphan designation, and will have written investigation brochures

What's on Offer

A fantastic opportunity to join a progressive business working with an enviable client base.

The opportunity to work remotely (with the occasional meeting in the UK based office).

Oliver Ross
Quote job ref
Phone number
+44 20 7269 6230

Job summary

Contract type
Consultant name
Oliver Ross
Consultant phone
+44 20 7269 6230
Job reference