Medical Writer II

Job Reference: #80135 Add to saved jobs

  • Salary £45000
  • Location Europe or South Africa, Home based
  • Permanent
  • Sector Pharmaceuticals

Job Summary

We are a global CRO looking for a Medical Writer II to join our close-knit team and support in a home-based capacity with our pharma clients. A successful candidate will have experience writing clinical documentation, including CSRs, protocols, and PIPs.

Job Overview

Who are we:
We are a leading full service CRO with our experience making us an invaluable partner to a large proportion of the industry, from top 10 pharma to virtual biotechs. One of our core markets is medical writing and as a result we have developed to be known as one of the leading organisations globally offering consultancy services in this area.

Key Responsibilities
Working as a medical writer in Europe your responsibilities will include:
• Critically evaluate, analyse, and interpret the medical literature
• Write and edit clinical development documents
• Complete writing assignments in a timely manner
• Maintain timelines and workflow of writing assignments
• Practice good internal and external customer service

Skills Required

Key Skills:
• Must have at least 18 months of industry regulatory writing and clinical medical writing experience
• The ideal candidate would hold a Bachelors, Masters, or Ph.D. in scientific, medical, clinical discipline
• Experience in regulatory submissions (clinical study reports) presented to regulatory authorities a plus
• Understanding of clinical data

Contact Details

Full job description and company details are available upon application, apply below. This position is being dealt with by Nicholas Rigden at Meet, please call on +44 (0) 2030195990. You can also e-mail us directly at to discuss in confidence.

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