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Regulatory Affairs Senior Associate - Oncology

£Negotiable DoE | Buckinghamshire |  Regulatory Affairs, Pharmaceutical Company/Sponsor side |  Permanent  | Ref:887874

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. 

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The Role

Regulatory Affairs Senior Associate - Oncology, Global Pharma, Bucks, £Negotiable DoE

 

The Company

A fantastic company with a great reputation working across established and novel pharmaceutical brands. They offer unique development opportunities and support people to further their career in the UK or globally.

  • Innovative, ideas-based company
  • Strong heritage in science
  • Culture of caring both internally and for patients
  • Agile and dynamic despite being a large corporation

 

The Role

As the Regulatory Affairs Senior Associate - Oncology, you will be responsible for; This role supports the regulatory managers in hands on development of technical files and dossiers for both CTA's and MAA's in the oncology therapy area.

  • Develop and maintain technical files and dossiers in preparation for submission
  • Manage MAA and CTA's across Europe, Middle East & Africa
  • Liaise with Regulatory agencies and local operating companies
  • Development, post approval and life cycle management across EMEA.

 

You

As the Regulatory Affairs Senior Associate - Oncology, you will have the following experience:

  • Good experience in regulatory affairs at an EMEA level
  • Experienced in submissions MAA and CTA's
  • Plus, you need to be dynamic, proactive and flexible with strong communication skills.
  • You will have a solid background within Oncology

 

What should you do next?

This Regulatory Affairs Senior Associate - Oncology 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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