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Senior Regulatory Medical Writer

Negotiable | Greater Manchester |  Client Services, CRO |  Permanent  | Ref:885438

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 / Manager, Negotiable Salary + Benefits, Greater Manchester

Looking for something more exciting than your standard Regulatory Writer position? Spent years churning out the same documents daily and now ready to take on additional responsibilities? 

 

The Company

Well-established European medical communications agency are expanding their UK office.

  • Excellent company culture, where performance and initiative are recognised and rewarded

  • List of employee benefits including performance related bonus scheme, 30 days annual leave and flexible working hours to name a few

  • Opportunity to travel across Europe attending client meetings

  • Working with several pharmaceutical and diagnostics clients

  • Highly competitive salary, negotiable for the right candidate

 

The Role

Sitting within the established Regulatory team, this is a highly varied role looking for candidates who will really use their own initiative, make the role their own and potentially move into a managerial position.

  • Writing and editing a range of regulatory and clinical documents including submissions, protocols, CSRs, PIPs etc.

  • Coordinating simultaneous projects

  • Contributing to and executing regulatory strategy

  • Liaising with clients, including negotiating of timescales, budgets and specifications

  • Taking an active role in business development to grow the Regulatory client portfolio

  • You will gain exposure and experience across a wide platform

 

You

To be considered for this vacancy, you will be able to demonstrate:

  • A minimum of five years Regulatory writing experience including submissions and clinical documents

  • A confident, personable approach when dealing with clients

  • Experience working to strict deadlines whilst managing projects

  • Mentoring / training team members

  • Business development experience highly beneficial

 

What should you do next?

This Senior Regulatory Writer / Manager 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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