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Regulatory Affairs Officer (CTA's)

£Negotiable DoE | Oxfordshire |  CRO |  Permanent  | Ref:887921

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

Regulatory Affairs Officer (CTA's) Leading Research Organisation, Oxfordshire, £Negotiable DoE

 

The Company

This is an exciting time to join a highly successful, leading research organisation in the heart of Oxfordshire They offer excellent training and development opportunities as well as great career progression opportunities.

  • Excellent career progression opportunities
  • Idyllic location with plenty of free onsite parking
  • Excellent training and development

 

The Role

As the Regulatory Affairs Officer (CTA's), you will be responsible for;

  • Regulatory and ethics submissions of clinical studies, preparing clinical trial submission dossiers
  • Facilitate the start of research projects of novel medicinal products
  • Communicate with regulatory authorities, ethics committees, project teams and vendors on regulatory-related matters
  • Manage safety reporting to authorities

 

You

As the Regulatory Affairs Officer (CTA's) you will have the following experience:

  • Previous regulatory / CTA experience
  • Preparation of clinical trial submission dossiers
  • Good experience / knowledge of regulatory affairs

 

What should you do next?

This Regulatory Affairs Officer (CTA's) 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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