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Regulatory Writer

£ompetitive package inc. bonus | North West, Cheshire |  CRO |  Permanent  | Ref:884040



Debbie Anderson

Which team do you work in?
I lead the development of our Clinical, Regulatory, PV, Quality and Manufacturing teams

Which area do you specialise in?

I focus on roles in Clinical Research and Pharmacovigilance. 

How do you keep up-to-date with the issues in your sector?

I participate in, and follow, industry news and conferences, such as DIA, and get involved in LinkedIn groups around my sectors. I learn mostly from day to day conversations with people working in these sectors.

What's your favourite film and why?

Ferris Bueller's Day Off. Shows my age but it's LOL before LOL was even invented! 

If you could invent one thing what would it be?

The ability to add extra hours into a day when you want to. And also the option to buy extra patience with small children!

What makes you #DistinctlyDifferent?

I've started trying acroyoga and adult gymnastics.….injuries are sure to follow! In business, I always want to make sure we are striving for improvement and doing things differently to other companies in ways that benefit our clients and candidates. Carrot is different by name and by nature!


The Role

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 an additional 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 Regulatory Writer, reporting into the Head of Regulatory Writing, you will be responsible for:

  • Authoring regulatory submission documents across various therapy areas e.g. Phase I & II Clinical Study Reports, Protocols, IB Updates.

  • Liaising with pharmaceutical clients and working to time & quality

  • Developing an understanding of timelines and interdependence of documents

  • Occasional ad hoc travel across Europe



The successful candidate will:

  • Regulatory writing experience (ideally but relevant transferable skills will be considered)

  • Have experience of liaising with clients (beneficial but not essential)


What should you do next?

This 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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