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Senior Regulatory Medical Writer

£Negotiable DoE | North West |  Regulatory Affairs, Pharmaceutical Company/Sponsor side, Regulatory Consultancy |  Permanent  | Ref:887884

The Role

Senior Regulatory Medical Writer, Leading Consultancy, North West £Negotiable DoE


The Company

This is an exciting time to join an expanding, highly successful consultancy in the leafy suburbs of Greater Manchester. They offer excellent training and development opportunities as well as great career progression opportunities.

  • Excellent career progression opportunities

  • Great training and development

  • Flexible working possible DoE for part of the week (not all)


The Role

As the Senior Regulatory Medical Writer, you will be responsible for;

  • Writing and editing regulatory and clinical documents, including protocols, CSRs,

  • submission dossiers, PIPs, etc

  • Creation of clinical documents in relation to regulatory projects and clinical studies

  • Managing and co-ordinating various regulatory writing projects



As the Medical Writer (Regulatory), you will have the following experience:

  • Previous regulatory / clinical writing experience (min 5 years ideally)

  • PhD/MD in medicine, life or health sciences, or pharmacy

  • Proven ability to work independently and under pressure, to strict deadlines


What should you do next?

This Senior Regulatory Medical Writer job is a great role and won't be around for long! So don't delay. If you are unsure and need some advice, give me a ring, otherwise just click apply, upload your CV and send, it's really that easy!

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.



Hayley Shayestehroo

Which team and area do you work/specialise in?

I work in the Regulatory Affairs team and recruit for Regulatory Affairs professionals at all levels within Pharma, Medical Devices companies and Regulatory Consultancies

What are some of the typical roles you cover?

I cover Regulatory Affairs positions at all levels within Pharma, Medical Devices and Regulatory Consultancies, these typically include;

Regulatory Affairs Associate jobs, Regulatory Affairs Executive jobs, Regulatory Affairs Senior Associate jobs, Regulatory Affairs Manager jobs, Regulatory Affairs Senior Manager jobs, Regulatory Affairs Director jobs, Regulatory Affairs Consultant jobs, Regulatory Writer jobs and Medical Writer jobs.

What are the hot issues in your sector currently?

Within Medical Devices it is the transition from MDD to MDR in May 2020. A lot of medical device companies are hiring Regulatory professionals to prepare their company for the transition

What’s makes you #DistinctlyDifferent?

I take pride in getting to know my candidates on a personal level as well as professional. Changing jobs is a big decision for most people so I like to ensure I am placing my candidates in a role that not only matches their career aspirations but also suits their personal situation and key motivations.


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