REGULATORY GRL - have US NDAs/ s/NDAs? Want to move up to a GRL role? Raleigh, Durham/ RTP/NC

Employer
Advanced S&S (USA)
Location
RTP Area, USA
Salary
On Application
Closing date
15 Oct 2020

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Discipline
Regulatory Affairs, Project Management, Regulatory Project Management
Hours
Full Time
Contract Type
Permanent
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REGULATORY GRL - have US NDAs/ s/NDAs? Want to move up to a GRL role? Raleigh, Durham/ RTP/North Carolina

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 the US  with / without international, and think this is the right step for your career.

You want to work on a Blockbuster to lead its 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 within the Raleigh, NC area, with some home working available (relocation available for the right candidate).

 

To Apply!

To apply for this role, please contact me, Theo Moore or Matt Greig on 855 505 1382, or send a full CV to CV@AdvTalent.com - please feel free to call us during working hours or on Saturday or Sunday AM (Eastern time)!

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 knows 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.

Contact us today to see how we can help you, make that next career move on

+44 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.

Advanced Regulatory is a new recruitment organisation. Our consultants are industry known and highly experienced in Regulatory Affairs recruitment. We have assembled a team with competencies in databased contingency recruitment, Search & Selection as well as Creative & Campaign management. Our specialism is Regulatory Affairs. We know that successful submissions are underpinned not by one but many people, all working in cohesion. Whether you require a new career position or a new recruit at junior, mid or senior level, we would like to assist you. Our remit is to provide Regulatory Affairs professionals at all levels to pharmaceutical, regulatory consulting, biopharmaceutical and clinical research organisations.

Contact Us
  • Suite 8, Penhurst House
  • 352-356 Battersea Park Road
  • SW11 3BY
  • GB
  • +1 855-505-1382
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