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Senior Regulatory Writer

£45k - £55k | UK |  CRO |  Permanent  | Ref:886802



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. 


The Role

Senior Regulatory Writer, £45k-£55k, Homebased - An opportunity to join a large multinational CRO


The Company

A highly successful, well-established CRO that specialise in providing clinical development services for pharmaceutical and medical device companies.

  • A very well-structured business with realistic potential for progression
  • Support & Sponsor EMWA
  • Close team & supportive management  


The Role

  • Home based or office based working as desired

  • Authoring of regulatory submission documents across a variety of therapy areas

  • Writing multiple clinical study reports and CTD documents or study protocols

  • Client liaison and meetings, including bid defences



  • The successful candidate will ideally have a minimum 3-4 years Regulatory writing experience

  • Educated to degree level in Life Sciences or equivalent

  • Experience of working in a pharmaceutical or CRO background

  • The ability to evaluate scientific data and report results accurately

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