REGULATORY GRL – have EU MAAs OR LEs? Want to move upto a GRL role? West London / M4 Corridor (code 619F)

Reference: MG050619F

Expiry Date: 05-02-2020

Categories Clinical Research, Regulatory Affairs

Salary: On Application

Job Type: Full Time

Location:
London
Greater London
United Kingdom

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Job Description

REGULATORY GRL – have EU MAAs OR LEs? Want to move upto a GRL role? West London / M4 Corridor

Please read the following and if this resonates with you then please apply to me, Matt Greig, or Theo Moore on +44 7918 679 405, or send a full CV to theo@advtalent.com - we support early evening calls if this is easier!

  • You want to work on a Blockbuster to lead it's final 2 clinical indications / label extensions before moving to another NME or new product
  • You like working in paediatrics or geriatric patient segments!
  • Experience in CNS or Neuro, Orphan, Seizure or Stroke useful
  • Director or Associate Director role
  • Comes with a bonus and RSU stock scheme
  • Well-known biopharma easily commuted from West of London, Middlesex, Surrey, Herts, or Bucks borders to Berkshire (you can work from home 2-3 days a week)

My client is seeking an individual who has at the very least, a good understanding of global drug development and registration (through involvement in project teams) and who now feels it is right to step up to a global regulatory leader role!

You will take over a submission preparation team, pre-submission, and take another indication through global filing, in a company where the GRL role sits with commercial, and supports directly the commercial and development leads.

The company has a strong pipeline, is led by experienced and well-known individuals who have a pedigree for development of their people and regulatory teams, that said, you will spend most of your time directly with the commercialization folks, and with your regulatory sub-teams.

The role is for someone who is able to manage the expectations of commercial and development partners while identifying opportunities with the business to bring both new markets and new indications to patients more quickly. After working on this high profile product, you will transition to a new NBE or recently registered product to work on a new set of life-cycle strategies (those with clinical studies dependant).

I would readily want to hear from you if you have relevant filing and approvals experience in Europe with / without international, and think this is the right step for your career.

 

To Apply!

To apply for this role, please contact me, Matt Greig, or Theo Moore on 44 7918 679 405 or +44 20 7801 3380, or send a full CV to theo@advtalent.com - we support early evening calls if this is easier!

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