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Principal Medical Writer

£Competitive salary and excellent benefits package | UK |  Regulatory Affairs, Pharmaceutical Company/Sponsor side |  Permanent  | Ref:887526

The Role

Principal Medical Writer - £Negotiable - Home Based

 

The Company

This is an exciting time to join an expanding, highly successful global pharma in a home based role.

  • Excellent career progression opportunities
  • Highly successful global pharma company
  • Great benefits with bonus, pension, healthcare to name a few

 

The Role

The Principal Medical Writer is responsible for;

  • Lead the medical writing activities for US and European regulatory submissions
  • Ensure documents for assigned clinical trials are prepared, reviewed and approved in a timely manner adhering to medical writing procedures / processes
  • Ensure clinical study reports, investigative brochures and other documentation are fully up to date and appropriate
  • Provides medical writing expertise for multiple projects in a specific therapy area

 

You

  • Proven track record in regulatory writing, regulatory submissions and clinical trials writing
  • Experience in clinical / preclinical data interpretation preferred
  • Oncology experience preferred desirable (other therapy areas will be considered)
  • Bachelor of sciences degree (or equivalent)
  • US & International regulations knowledge preferred

 

What should you do next?

This Principal 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.

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’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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