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Principal Medical Writer (Regulatory)

£negotiable | Buckinghamshire |  Regulatory Affairs, Pharmaceutical Company/Sponsor side |  Permanent  | Ref:889487

The Role

Principal Medical Writer (Regulatory) - Global Pharmaceutical Client - High Wycombe (remote working available) - £negotiable

Principal Medical Writer (Regulatory) responsible for preparing and finalising scientific and clinical documents at the highest quality inline with established timelines and processes.

 

The Company

My client is a global pharma company covering multiple therapy areas. Based in High Wycombe, this company operate on a global scale and are at the forefront of what they do.

  • Global, leading pharma company
  • Covering multiple countries across the globe
  • Flexible working
  • Great career progression
  • Diverse range of projects / products to work on

 

The Role

The Principal Medical Writer (Regulatory) will be responsible for;

  • Preparing and finalising scientific and clinical documents at the highest quality inline with established timelines and processes Ensure product compliance to REACH and other relevant legislation
  • Managing writing projects
  • Setting strategies within timeline constraints
  • Mentor a team of contractors

 

You

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

  • At least 5 years' experience in medical writing (regulatory)
  • Experience writing clinical regulatory submission / safety documents, CSR's, Investigative Brochures, CTDs
  • Good project management experience
  • Good knowledge of the end to end drug development process

 

What should you do next?

This Principal Medical Writer (Regulatory), role is one not to be missed; it encompasses the opportunity to work with new and exciting products within a company who are at the forefront of pharma and biocides. 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.

Consultant

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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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