select * from applications_reporting where candidate_id = '' 3

Regulatory Ops SME / Regs Publishing Consultant

£DoE + Package | London |  CRO |  Permanent  | Ref:887110

Consultant

image

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 Operations SME / Regulatory Publishing Consultant, Regulatory Consultancy, London, £DoE + Package

 

The Company

A global regulatory consultancy who work with a vast portfolio of clients and support career development. A privately owned company with offices across London and the US.

  • Privately owned company

  • An impressive client base across the globe

  • Offices in London and the US

  • Focused on regulatory strategy, regulatory intelligence and building a solution for clients

 

The Role

The Regulatory Operations SME / Regulatory Publishing Consultant will ensure everything is set up for the end to end process for post clinical product lifecycle management processes.

  • Content creation, publishing, submission, regulatory information management

  • Regulatory strategy

  • Regulatory intelligence

  • Working with external pharmaceutical brands

 

You

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

  • European regulatory affairs experience
  • End to end regulatory operations

  • Publishing and submissions

  • Related processes - MAA, Variations, Annual Reports, PSUR, Renewals

  • Knowledge of external pharmaceutical data standards

 

What should you do next?

This Regulatory Operations SME / Regulatory Publishing 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.



More jobs like thisSee all