OPTION BELGIQUE ** Global RA Lead ** EU MAAs OR Line Extensions? Next step GRL role? Relo offered
- Experience Level
OPTION BELGIQUE ** Global Regulatory Lead ** EU MAAs OR Line Extensions? Next step GRL role? Relocation offered
Please read the following and it 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 email@example.com - 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, has a good understanding of global drug development and registration (through involvement in project teams) and who now feels it is the right time 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, please contact me, Matt Greig, or Theo Moore on +44 7918 679 405 or +44 20 7801 3380, or send a full CV to firstname.lastname@example.org - we support early evening calls if this is easier!
About Advanced Search & Our Network
Advanced Search, has a network of affiliated companies including ADV Regulatory, and ADV Talent Partners. Together, we are specialists in Regulatory Affairs and Life Sciences recruitment especially around mAbs and biologicals for roles in R&D and Commercialization and have been established and hiring in this area since 2005.
Our team know our subject matter areas and our mission is to help you grow your career each and every step of the way. We have helped many of today's leading companies develop strong regulatory sciences functions and are known for hiring complimentary teams that work well with each other, at owner-contributor, strategy leading and people management levels.
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+44 (0)20 7801 3380
All applications are kept in confidence and we invite applications from all members of the Academic, Research & Development based bio-/pharmaceutical community.
Keywords / Key words: Regulatory Affairs, RA, RA Jobs, Regulatory Affairs Jobs, RA Manager, Regulatory Jobs, Regulatory, RA Director, RA Associate Director, Pharmaceutical, Pharma, Bio-pharmaceutical, Bio-technology, RA GRL Jobs, Snr Regulatory Affairs
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