US Liaison, Take the NEXT step to become a GRL – RTP, North Carolina

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

View more

Discipline
Regulatory Affairs, Project Management, Regulatory Project Management
Hours
Full Time
Contract Type
Permanent
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US Liaison, Take the NEXT step to become a GRL – RTP, North Carolina

Are you looking for a role that will utilise your US liaison experience to be promoted GRL?

My client has multiple indications in different stages of development and is recruiting for US leaders/liaisons who want to become GRL’s.

Regulatory Affairs US liaison - great chance to become a Global Regulatory Leader.  Based in RTP North Carolina.

We are now hiring for an experienced US liaison, regulatory strategist and regulatory project manager who wants to take the next step to become a GRL. You will have already established your career level as a Regulatory Liaison or RA Leader, and now want to establish yourself on the global strategy level where you are responsible for the global strategy document, and for co-defining with the partners, the clinical development and regulatory pathway for NMEs in early and/or late phase development. This group is therapeutically aligned and they have a broad range of indications in different stages of development.

This role is focused on developing the value for the molecule, identifying potentials for speedier or parallel development, adaptive or innovative pathways for both the EU and US regions …. and more! 

You will you use your experience and expertise to shape the direction of your indications globally, in matrix teams that also have profit and loss/financial reasonability for their proposed programmes.

Personality wise, you will have a friendly and engaging personality, willing to work with senior leaders from market access, brand marketing, clinical and quality to generate new ideas and shape existing ones. You will be a team player, but know how to influence individuals to steer programmes, in a company which has a strong matrix.

Experience-wise, US exposure is useful, as you can imagine, but the requirement is you have some actual strong late phase development and / or extensive NDA experience and understand how regulatory can lever their know-how to drive drug development and initiate and manage useful health authority interactions.

We have options on grade, so you can be interested in either an Associate Director or Director grade.  My client is based in RTP North Carolina.
 

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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