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Senior Medial Writer

£negotiable | UK |  Regulatory Affairs, CRO |  Permanent  | Ref:889385

The Role

Senior Medial Writer - Regulatory/Clinical - Global CRO - Homebased - £negotiable 

Senior Medial Writer - Regulatory/Clinical, responsible for researching, creating and editing all documents associated with clinical research.

 

The Company

My client is a CRO covering multiple therapy areas. Based in the South East, this company have an exciting and broad variety of projects to work on.

  • Global, leading CRO
  • Home based position
  • Great career progression

 

The Role

The Senior Medial Writer - Regulatory/Clinical will be responsible for researching, creating and editing all documents associated with clinical research.

  • Writing Clinical Study Reports, Protocols, Informed Consent to Clinical Overviews etc
  • Managing multiple projects
  • Reviewing all documentation to a high standard

 

You

To apply for this role as a Senior Medial Writer - Regulatory/Clinical, our client is hoping for someone with the following skills and experience;

  • 2 years' experience within a CRO Medical writing position
  • Good stakeholder management
  • Can work independently
  • Degree educated in life sciences

 

What should you do next?

This Senior Medial Writer - Regulatory/Clinical 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 clinical research. 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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