Regulatory Affairs Senior Manager & Associate Director roles/US Liaisons - North Carolina or Georgia

North Carolina or Georgia
09 Oct 2019
08 Nov 2019
TM/190919 R2
Theo Moore
Full Time
Contract Type
Experience Level

Regulatory Affairs Senior Manager & Associate Director roles/US Liaisons - North Carolina or Georgia

Location: North Carolina or Georgia

Regulatory Affairs Snr Mgr or Associate Director, based in North Carolina or Georgia - Utilise your US RA experience to develop towards being a GRL. 

REGULATORY ** Do you want to use your US RA experience to develop towards being a GRL? ** We have a number of new position working in early and mid-stage development, incl. mAbs. graded at Regulatory Affairs Senior Manager and Regulatory Affairs Associate Director.

Do you see yourself as an aspiring regulatory professional with a keen interest in consolidating what you have learnt, and applying yourself further to develop and stretch your skills? Alternatively, you could be ‘there already’ and want to move because your current organization has plateaued so you know want a fresh challenge, a new project or product!

We have options on grading with 2 levels of grade, so it is very likely we can meet your expectations as we can hire at both Senior Manager and Associate Director levels. Relevant points to consider about this organization are:-

  • GRL Pathway: firstly, our client offers the Global Regulatory Leader career pathway AND a people management pathway in this function, so whether you want to develop more global expertise or alternatively move into a team management role, BOTH of these options are open to you
  • Vision: The line management is strong, thinks long-term, advocates for their staff and for regulatory to collaborate as a strategic partner (having won this idea a long time back), so you will be able to use your 'regulatory voice’ in this role, in defining US RA strategy!
  • Drug Pipeline: mostly m/f/Abs, so novel, innovative, so you will work on NMEs which are large molecule drugs mostly normally with quicker development pathways than traditional NCEs
  • In-house R&D: refreshingly this is not a virtual company, where NMEs are bought, so discovery and research is well-funded and overall added with the clinical development costs, this company is investing a healthy >20% on R&D! As well as a variety of people to learn from, and although the company has a track record of developing regulatory professionals, with many of the GRLs being home-grown, this is also augmented by ex-FDA Regulators and Regulatory Professionals from other major companies including the top 5 organizations and speciality pharmaceutical companies.

To apply for this role, you will have a minimum of 5 years' experience in regulatory affairs, covering US development and NDA activities for small molecules or Biologicals.

A full relocation package is available to you, depending upon your location and situation.


To apply, please send a full CV to, or alternatively, contact Theo Moore on US toll free 855-505-1382. We are assigned these roles by our client and will provide you with support throughout the hiring process.



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.

All applications are kept in confidence and we invite applications from all members of the Academic, Research & Development based bio-/pharmaceutical community.

We provide a high level of service because we believe this matters.

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