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Regulatory Affairs Associate Director

£Competitive salary plus car allowance, bonus and benefits package | South East, Buckinghamshire |  Pharmaceutical Company/Sponsor side |  Permanent  | Ref:886930

Consultant

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Debbie Anderson

Which team do you work in?
I lead the development of our Clinical, Regulatory, PV, Quality and Manufacturing teams

Which area do you specialise in?


I focus on roles in Clinical Research and Pharmacovigilance. 

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


I participate in, and follow, industry news and conferences, such as DIA, and get involved in LinkedIn groups around my sectors. I learn mostly from day to day conversations with people working in these sectors.

What's your favourite film and why?

Ferris Bueller's Day Off. Shows my age but it's LOL before LOL was even invented! 

If you could invent one thing what would it be?

The ability to add extra hours into a day when you want to. And also the option to buy extra patience with small children!

What makes you #DistinctlyDifferent?

I've started trying acroyoga and adult gymnastics.….injuries are sure to follow! In business, I always want to make sure we are striving for improvement and doing things differently to other companies in ways that benefit our clients and candidates. Carrot is different by name and by nature!

More

The Role

Regulatory Affairs Associate Director - Leading Pharmaceutical Company - Buckinghamshire - £Competitive salary plus car allowance, bonus and benefits package

 

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

This role leads regulatory strategy in the oncology therapy area for development, post approval and life cycle management across EMEA.

  • Advise Global Regulatory Lead on strategy and approach in EMEA.

  • Lead MAA and CTA's across Europe

  • Liaise with Regulatory agencies and local operating companies

  • Line manage 1-2 managers/contractors

 

You

Will have extensive strategic regulatory affairs experience at a European/regional level, have lead MAA and CTA's independently and been involved or responsible for project strategy. Plus, you need to be dynamic, proactive and flexible with strong communication skills.

 

What should you do next?

This Regulatory Affairs Associate Director 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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