Regulatory Affairs CMC Snr Manager - Use your EU exp. to gain GRL status

Advanced Regulatory (UK & Europe)
London, M4 Corridor
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 Snr Manager - Use your EU exp. to gain GRL status

EU and then global role covering development projects, P2/3 to MAA

This is a rare opportunity where you can grow and develop to be the lead for both EU and US markets, for small and/or large molecules in a medium sized organization with a structure that likes to give regulatory staff the opportunity to reach their potential.

This role is focused on taking the lead for strategic development activities initially in the EU but with growth opportunities to also work on US projects.

Location: close to Maidenhead, commutable Reading, Slough, Uxbridge, High Wycombe and London.  Great transport links and close to a mainline train station, with company bus service from station to the offices.

This rapidly expanding organization has a reputation for giving opportunities to those who show promise and ambition and it’s a fast paced environment where you stand a greater chance of being noticed for your contribution than in a larger organization where you can easily become pigeon holed.   You can easily interact with upper management and expect to be given the opportunity to be involved in multiple projects, where you will gain more experience.

The regulatory department here is part of the Global RA department, so expect to be involved in key strategic decisions for all major markets. You will be encouraged to become a strong performer, and as a result you will receive faster promotions and regular pay increases.

The culture here is based around creating an environment where people want to work, where people feel empowered to be a success and where people are moving in the direction that they want. The focus here is on better team work and co-operation with a focus on getting work done and less politics.

In the short-term you will be working on clinical development projects in Phases 2 and 3 as the Regulatory CMC lead, guiding these projects through to MAA. In the longer term you will have the opportunity to work in a global role as a GRL or move into early development position and gain experience across the full project lifecycle.

Role / Responsibilities:

Defining strategy, planning and preparation of regional specific CMC submission documentation for assigned geographical regions and contributing to the preparation of global submission documentation to deliver timely approvals to meet business needs.

  • Representing CMC on Global Regulatory Affairs Teams, for assigned projects/products.
  • Leading and/or providing regulatory CMC input to all Health Authorities (HA) interactions on CMC.
  • Leading or providing input to internal regulatory business initiatives and cross functional work streams as assigned.

The package for this role is extremely generous and includes a top level salary, bonus of up to 15% per annum, with a high level benefits package which includes a-grade health insurance, strong pension, dental, death in service, options to work from home.

To Apply!

To apply, please send a full CV to, or alternatively contact Theo or Oli 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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