OPTION BELGIQUE ** Global Regulatory Lead ** EU MAAs OR Line Extensions? Next step GRL role? Relocation offered (code 619E1)

Reference: MG050619E1

Expiry Date: 05-09-2021

Categories Biotech, Clinical Research, Regulatory Affairs

Salary: On Application

Job Type: Full Time


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Job Description

OPTION BELGIQUE ** Global Regulatory Lead ** EU MAAs OR Line Extensions? Next step GRL role? Relocation offered

Please read the following and if this resonates with you then please call me, Matt Greig, or Theo Moore on +44 7918 679 405 - we support early evening calls if this is easier!

This role is based in Belgium, and full support is provided for relocation from any EU Member State:-

  • 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 car, petrol card, bonus and RSU stock scheme
  • support for relocation! Tax reduction package offered for incoming applicants.

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 press the red ''Apply'' button or contact me, Matt Greig, or Theo Moore on 44 7918 679 405 or +44 20 7801 3380 - we support early evening calls if this is easier!

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