Medical Writer - Clinical / Regulatory

4706159
  • Job type

    Contract
  • Location

    Milton Keynes
  • Working Pattern

    Full-time
  • Specialism

    Regulatory Affairs
  • Industry

    Scientific and R&D
  • Pay

    £350 - £425 p/d

Contract - Regulatory / Clinical Medical Writer - Medical Device / Pharma Company

Your new company

My client, a leading innovator in the medical device industry, dedicated to improving patient outcomes through cutting-edge technology and rigorous scientific research, is looking for a talented and detail-oriented Regulatory /Clinical Medical Writer to join their team for a 6-month initial contract.


Your new role

As the Regulatory/ Clinical Medical Writer, you will be involved in the development, writing and editing of regulatory and clinical documents such as protocols, Clinical Study reports, regulatory submissions and Investigator brochures. You will conduct literature reviews and summarise findings to support clinical and regulatory documents and participate in project meetings and provide input on document strategy and content.


What you'll need to succeed

In order to apply for the Medical Writer contract, you must possess:
- Bachelor's degree in a scientific discipline; advanced degree is preferred
- MUST HAVE significant experience in writing regulatory and clinical documents such as protocols, CSRs, IB, regulatory submissions, in the medical device or pharmaceutical industry
- Strong understanding of clinical research and regulatory requirements for medical devices
- Excellent writing, editing, and proofreading skills, with keen attention to detail.
- Ability to work independently and manage multiple projects with tight deadlines.
- Proficiency in Microsoft Office Suite and familiarity with document management systems.
- Strong communication and interpersonal skills.
- Experience with regulatory submissions (e.g., FDA, EMA, MHRA).
- Certification from the American Medical Writers Association (AMWA), European Medical Writers Association (EMWA) or similar organisation.


What you need to do now

Please submit your resume, cover letter, and writing samples.
Before you apply for this position, it is vital that you are in possession of a UK passport or relevant visa to work without restrictions in the UK and must be based in the UK.

To apply for this position or if you want to discuss other roles that we are working on, please do not hesitate to contact Roberta Atkins on 0333 010 6292.

Apply for this job

Talk to Roberta Atkins, the specialist consultant managing this position

Located in London-City, 5th Floor, 107 Cheapside, Telephone 03330106292
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