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Senior/Principal Regulatory Writer

£Competitive package inc. bonus | North West, Cheshire |  CRO |  Permanent  | Ref:884041

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/Principal Regulatory Writer, competitive package inc. bonus fantastic benefits, Cheshire.

A Cheshire based healthcare communications agency with a specific focus on regulatory writing services are experiencing rapid growth and therefore require a Senior or Principal Regulatory Writer to join their Regulatory team.

 

The Company

Working with a number of high profile pharmaceutical clients writing documents for regulatory submissions.

  • Friendly and supportive team environment in open place office

  • Offering a varied workload across numerous therapy areas

  • Free onsite staff parking and shuttle bus to local train station

  • Offering some flexibility with regards to homeworking

 

The Role

As the Senior or Principal Regulatory Writer, you will be:

  • Authoring complex regulatory submission documents across various therapy areas e.g. Clinical Summaries (at Principal level; Clinical Overview)

  • Fully client facing with management of project teams (Line management if Principal)

  • Budgetary responsibilities

  • Supporting and developing junior team members with regulatory knowledge

  • Occasional ad hoc travel across Europe

 

You

The successful candidate will:

  • Extensive Regulatory writing experience

  • Client liaison and project management experience

  • For Principal - Mentoring or line management experience

 

What should you do next?

This Senior/Principal Regulatory 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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