Regulatory Affairs CMC Senior Manager, Biologicals - Early Dev. Clinical Lead - Global Role, UK

Advanced Regulatory (UK & Europe)
Berkshire, UK
Closing date
14 Oct 2020

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Regulatory Affairs, CMC, Compliance, Project Management, Regulatory Project Management
Full Time
Contract Type
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Regulatory Affairs CMC Senior Manager, Biologicals - Early Dev. Clinical Lead - Global Role, Berkshire

We have a great new role with a dynamic and expansive Global biotechnology company offering a  great opportunity for a Regulatory Affairs CMC Senior Manager to work in a broad based role across a number of really interesting biological products.

Why is this a good role?

There are many programs in development including mAbs, breakthrough drugs, Cell and Gene therapy products….which makes it an exciting time to join! It’s also a Global role so you will have input on EU and US strategy and also have a great opportunity to progress to Associate Director grade.

About My Client

Few biotechnology companies have seen such a steady rise in terms of their turnover or high value assets as my client, whom have double in size every 4 years in the last 15.  Sales are well over 15Billion a year and steadily increasing year on year and they have over 25 indications currently running in development.

This organization has developed successful therapeutics in all of the modalities, small and large molecules, oligos, viral vectors, they continue to be at the forefront in terms of registrations of the newer sciences, and have a pipeline which is very novel, they are not unwilling to go after some of the most stubborn disease areas.

Your Background & The Role

This is an early stage development role, so some experience of working on early stage products is needed, but candidates with P3 experience will also be considered.  A flexible approach is needed and there is also the chance that you could also lead or support a MAA/BLA in the future as my client likes to help its RA CMC team members to expand and develop their knowledge and expertise.

Soft skills needed include good coordination, good communication skills, the ability to make deadlines and to be a team player. Experience of negotiating and answers questions form HA’s is needed and any Scientific Advice meeting experience would be welcome.

Package & Benefits

You will be offered a strong basic salary with a high level bonus, car allowance and lucrative share package, to make this arguably the strongest package available at Snr manager grade in the UK.

To Apply!

To apply, please send a full CV to, or alternatively contact Theo Moore or Oli Dimitrov on +44 (0)207 801 3384 or +44 (0)207 801 3388. 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 Regulatory Affairs team know their 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 (0)207 801 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
  • +44 (0)20 7801 3380
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