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Senior Regulatory Writer

£30k-£40k bonus | North West, Cheshire |  Pharmaceutical Company |  Permanent  | Ref:884041

Consultant

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Katie Goulbourn

Which team do you work in?
I work within the Drug Development team.

Which area do you specialise in?
I specialise in recruiting Junior to Director level Regulatory Affairs & Quality Assurance professionals within Pharma, Healthcare, Medical Devices and Animal Health. 

How do you keep up-to-date with the issues in your sector?
Speaking daily with clients and candidates keeps me on top of the latest industry trends and news, combined with regularly visiting relevant websites and reading articles.

What's your favourite film and why?
I absolutely love a good rom-com, my favourite would have to be The Holiday.

If you could invent one thing what would it be?
Trackable GPS microchips for cats and dogs - how has this not been invented yet!?

More

The Role

Senior Regulatory Writer, £30k-£40k 8%-12% bonus fantastic benefits, Cheshire

A Cheshire based healthcare communications agency, specialising in communication planning and regulatory services are experiencing rapid growth and therefore require an additional Senior Regulatory Writer to join their Regulatory team.

 

The Company

  • Working with a number of high profile pharmaceutical clients providing regulatory submissions and clinical documents.

  • Friendly team environment in open place office including Directors

  • Offering a varied workload across numerous therapy areas

  • Free onsite staff parking and within walking distance of the local train station

  • Extensive list of company benefits including annual profit-related bonus (target of 8%-12%), 5% pension contribution, health insurance, 25 days annual leave bank holidays, life cover and critical illness cover.

  • Offering some flexibility with regards to homeworking

 

The Role

As the Senior Regulatory Writer, reporting into the Head of Regulatory Writing, you will be responsible for:

  • Authoring of regulatory submission documents across various therapy areas

  • Working on behalf of pharmaceutical clients

  • Liaising with clients via phone, webex and face to face meetings across Europe and occasionally the US

  • Preparing clinical study reports

 

You

The successful candidate will have:

  • A minimum of 3 years Regulatory writing experience within a client facing role

  • Experience contributing to strategic Regulatory planning

  • Experience authoring and preparing CTD and clinical study reports

  • The ability to evaluate scientific data and report results accurately

  • Experience supporting more junior members of the team

 

What should you do next?

This Senior 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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