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Global Regulatory Operations Senior Associate

£DoE | South East |  Pharmaceutical Company/Sponsor side |  Permanent  | Ref:887340

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

Global Regulatory Operations Senior Associate / Global Pharma, South East, £DoE

 

The Company

A global pharma who work within a specialist therapy area and support career development. They boast offices across the globe and are committed to ensuring patients have access to quality treatments.

  • Global specialist pharma company

  • Offices worldwide

  • Specialist therapy area

  • Proven success with their core products

 

The Role

The Global Regulatory Operations Senior Associate will ultimately be responsible for providing support to publishing and submissions for all related projects.

  • Provide regulatory submission guidance and support to relevant project teams

  • Prepare and file relevant product registrations

  • Provide support for electronic submission documents (eCTD and NeeS)

  • Work to strict timescales / deadlines

 

You

You will have regulatory operations experience as well as good knowledge and experience of the following;

  • Regulatory operations / regulatory publishing

  • Document management and electronic submissions

  • Experience with Acrobat based PDF QC Tools (i.e. D2, Documentum, ISIToolbox)

  • eCTD Publishing tools

 

What should you do next?

This Global Regulatory Operations Senior Associate 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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