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Regulatory Writing Manager

£Competitive salary and benefits | Oxfordshire |  Regulatory Affairs, Pharmaceutical Company/Sponsor side |  Permanent  | Ref:887390

Consultant

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Hayley Shayestehroo

Which team do you work in?

I work in the Regulatory Affairs team.

Which area do you specialise in?

I specialise in recruiting all levels of Regulatory Affairs professionals within pharma, healthcare and medical devices. 

How do you keep up-to-date with the issues in your sector?

Speaking to candidates is the best way to keep updated with changes in the market. I also like to read relevant industry press and relevant articles on LinkedIn. 

What's your favourite film and why?

Mrs Doubtfire - it's an all time classic and I pretty much know it word for word. I love a good thriller too, anything with a good twist at the end. Law Abiding Citizen with Gerard Butler is one of my faves. 

If you could invent one thing what would it be?

Pizza that makes you slim! 

What makes you #DistinctlyDifferent?

I love watching pretty much any sport. I play netball twice a week and come from a footballing family, so have been taught how to do kick ups (my record is 21 without hitting the floor!) Work wise, I like to think I get to know candidates on a deeper level and really understand their drivers and motivations for moving to another company. 

More

The Role

Regulatory Writing Manager £Negotiable, Oxfordshire

 

The Company

This is an exciting time to join an expanding, highly successful global pharma based at their Oxfordshire site.

  • Excellent career progression opportunities
  • Specialised global pharma company
  • Great benefits with bonus, pension, healthcare,

 

The Role

The Regulatory Writing Manager 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

 

You

  • Proven track record in regulatory writing
  • Experience working on summary level documents (investigative brochures / regulatory submissions)
  • Proven ability to manage multiple projects at once
  • Life sciences degree (or equivalent)
  • Experience in Oncology or Neuroscience in desirable (other therapy areas will be considered)

 

What should you do next?

This Regulatory Writing Manager 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.



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