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Regulatory Writer – International Consultancy – Remote (UK based) - £negotiable

This is an exciting time to join an expanding, highly successful Consultancy on a permanent basis based in South Manchester / Cheshire, however the role can also have some remote working. They offer excellent training and development opportunities as well as great career progression and an excellent work/life balance.  This role is based in Cheshire but can also involve remote working (UK only) and can also offer part time options if required (30 hours/4 days).

The Company

An independently owned, international consultancy is now recruiting for a Regulatory Writer to join them on a full or part time basis, based remotely in the UK.

  • Independently owned company
  • Excellent career progression opportunities
  • Great training and development
  • Exciting and innovative projects
  • Grown at a very impressive rate over the last 12 months

The Role

The Regulatory Writer will have the opportunity to work with well known, innovative pharmaceutical companies across a range of therapy areas.

  • Plan and deliver regulatory submissions on behalf of pharmaceutical clients
  • Prepare clinical regulatory documents across multiple therapy areas
  • Evaluate scientific data
  • Work on projects independently as well as group projects


To apply for this role as Regulatory Writer our client is hoping for someone with the following skills and experience

  • Ample regulatory writing experience within a pharmaceutical company, CRO or Consultancy
  • Experience writing clinical regulatory documents to a high standard
  • Strong understanding of clinical development and ICH guidelines
  • Experience authoring regulatory documentation such as CTD modules, response documents and regulatory briefing documents
  • Degree educated in life sciences / pharmaceutical science

What should you do next?

This Regulatory Writer role is one not to be missed; it encompasses the opportunity to work in a fast-paced environment on new and exciting projects. To discuss this role or other live Regulatory Affairs jobs further, please submit your current CV or give me a call today.

Unless otherwise stated, if applying for a job within the European Union, you must ensure that you are already authorised to work there.

Carrot Pharma Recruitment Ltd acts as an Employment Business and an Employment Agency on behalf of our client in recruitment for this role.

Apply Now!

Job Consultant

Hayley Shayestehroo

Regulatory Affairs

Senior Consultant

01625 361072

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