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Senior Regulatory Medical Writer

£Negotiable DoE | North West |  Regulatory Affairs, Pharmaceutical Company/Sponsor side, Regulatory Consultancy |  Permanent  | Ref:887884

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. 

More

The Role

Senior Regulatory Medical Writer, Leading Consultancy, North West £Negotiable DoE

 

The Company

This is an exciting time to join an expanding, highly successful consultancy in the leafy suburbs of Greater Manchester. They offer excellent training and development opportunities as well as great career progression opportunities.

  • Excellent career progression opportunities

  • Great training and development

  • Flexible working possible DoE for part of the week (not all)

 

The Role

As the Senior Regulatory Medical Writer, you will be responsible for;

  • Writing and editing regulatory and clinical documents, including protocols, CSRs,

  • submission dossiers, PIPs, etc

  • Creation of clinical documents in relation to regulatory projects and clinical studies

  • Managing and co-ordinating various regulatory writing projects

 

You

As the Medical Writer (Regulatory), you will have the following experience:

  • Previous regulatory / clinical writing experience (min 5 years ideally)

  • PhD/MD in medicine, life or health sciences, or pharmacy

  • Proven ability to work independently and under pressure, to strict deadlines

 

What should you do next?

This Senior Regulatory Medical Writer 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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