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Senior Regulatory Affairs Consultant

£Negotiable DoE | London |  Pharmaceutical Company/Sponsor side |  Contract  | Ref:887812

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

Senior Regulatory Affairs Consultant - Startup Pharma - London - £Negotiable DoE

 

The Company

This is a great time to join an exciting pharma start-up in the heart of central London on an initial 3-month contract basis. This role would suit a Regulatory Consultant who would be happy contracting for around 2-4 days per month initially.

  • Great start-up Pharma client

  • City location close to major transport links

  • Exciting projects to work on / manage

 

The Role

As the Senior Regulatory Affairs Consultant, you will be responsible for;

  • Managing the regulatory lifecycle end to end for a new, exciting product

  • Liaising regularly with the relevant bodies MHRA etc

  • Ensuring products adhere to relevant regulations / legislations

 

You

You will have the following experience:

  • Familiar with UK regulatory bodies i.e. MHRA

  • Experience in licences medicines/ specials ideally

  • Happy in a hands-on role

  • Ideally experienced in cannabinoid based products but this is not a prerequisite

 

What should you do next?

This Senior Regulatory Affairs Consultant 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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