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Regulatory Affairs Medical Writer (Medical Devices)-

£Competitive | North West, Cheshire |  Regulatory Affairs, CRO |  Permanent  | Ref:889165

The Role

Regulatory Affairs Medical Writer (Medical Devices) - CRO - Cheshire - £Competitive

This is an exciting time to join an expanding, highly successful CRO in their offices in Cheshire. They offer excellent training and development opportunities as well as great career progression opportunities.

  • Excellent career progression opportunities
  • Great training and development
  • Exciting and innovative product / therapy range


The Company

This is an exciting time to join an expanding, highly successful CRO based at their Cheshire site.

  • Privately owned global CRO
  • Extensive and exciting projects covering multiple therapy areas / products
  • Great location with ample parking available


The Role

The Regulatory Affairs Medical Writer (Medical Devices)- will be responsible for creating high quality regulatory documents for pharma and medical devices clients (across multiple therapy areas)

  • Creating regulatory documentation for medical devices or pharma clients
  • Ensuring projects adhere to ICH GCP standards
  • Developing and preparing regulatory documents, trial documentation, patient information leaflets, CSRs and medical information documents



To apply for this role as a Regulatory Affairs Medical Writer (Medical Devices) our client is hoping for someone with the following skills and experience;

  • Prior clinical trials regulatory affairs experience (CRO or Pharma)
  • Medical Devices
  • Medical writing
  • Ideally degree educated in Life Sciences


What should you do next?

This Regulatory Affairs Medical Writer (Medical Devices) role is one not to be missed; it encompasses the opportunity to work in a fast paced environment on new and exciting products. To discuss further, please submit your current CV.

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 is your greatest fear?

I don’t really have one, but if there’s one thing I’m well not keen for it would be snakes or an army of ants…


How would your friends describe you in three words?

Funny, healthy, sporty


You’re stranded on a desert island – what one thing could you not live without?

Bear Grylls! He’d have us rescued in no time!


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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