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Global Regulatory Affairs Senior Associate

£Competitive salary and benefits | Yorkshire & The Humber |  Pharmaceutical Company/Sponsor side |  Permanent  | Ref:886878

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

The Company

This is an exciting time to join an expanding, highly successful global healthcare company based at their Yorkshire site.

  • Fantastic refurbished offices with many facilities including staff shop, canteen, subsidised coffee shop and dry cleaners.

  • Excellent career progression opportunities

  • City location with plenty of free onsite parking

  • Great benefits with bonus, pension, healthcare, share scheme and discounted products.

 

The Role

  • Lead product integrity review across a wide product portfolio for all global markets.

  • Assess regulatory status of products

  • Identify regulatory requirements, changes, risks and threats

  • Lead small team of regulatory associates

 

You

  • Have a minimum of 2 years' experience working in regulatory lifecycle management.

  • Quality background useful

  • Global or EU experience

  • Proven ability to manage numerous projects to deliver on time

  • Be confident, energetic, with a can do attitude

 

What should you do next?

This Global Regulatory Senior Associate 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.