REGULATORY ** Use your US RA experiences to develop towards being a GRL? **

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

View more

Discipline
Regulatory Affairs, Project Management, Regulatory Project Management
Hours
Full Time
Contract Type
Permanent
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R E G U L A T O R Y ** Use your US RA experiences to develop towards being a GRL? ** New position working in early stage development, incl. mAbs

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 and because 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 Senior Manager or 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, more for the more senior grading, and be willing to either work remotely with travel often to HQ, or be willing to relocate or live near RTP / Raleigh Durham, NC.

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

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.

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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