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Senior Regulatory Writer

£45k - £55k | UK |  CRO |  Permanent  | Ref:886802

Consultant

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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!

More

The Role

Senior Regulatory Writer, £45k-£55k, Homebased - An opportunity to join a large multinational CRO

 

The Company

A highly successful, well-established CRO that specialise in providing clinical development services for pharmaceutical and medical device companies.

A very well-structured business with realistic potential for progression

Award winning company

Works across over 30 countries

 

The Role

  • Home based working

  • Authoring of regulatory submission documents across a variety of therapy areas

  • Writing multiple clinical study reports and CTD documents or study protocols

  • Allows you to take ownership of your own work

 

You

  • The successful candidate will have Minimum 4 years Regulatory writing experience

  • Educated to degree level in Life Sciences or equivalent

  • Experience of working in a pharmaceutical or CRO background

  • The ability to evaluate scientific data and report results accurately

 

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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