Head of Regulatory CMC Policy (Global Role) ** South-East / M4 Corridor or Central London

Employer
Advanced Regulatory (UK & Europe)
Location
South-East, M4 Corridor
Salary
Competitive
Closing date
14 Oct 2020

View more

Discipline
Regulatory Affairs, CMC, Compliance, Project Management, Regulatory Project Management
Hours
Full Time
Contract Type
Permanent
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Head of Regulatory CMC Policy (Global Role) ** South-East / M4 Corridor or Central London

Few biotechnology companies have seen such a steady rise in terms of their turnover or high value assets as my client, whom have doubled in size every 4 years in the last 15.

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.

This role is a newly created position to build on their existing footprint for CMC sciences, CMC regulatory, both in policy and policy forums.

The role is for an individual who has experience of being part of agency side policy development for CMC or being in a company or association influencing policy from the sponsor side.

Your Background & The Role

The opportunity is to now join my client and bring together their internal experts, map the policy against the topics and lay out a strategic plan to lever their footprint and become a strong player in policy forums and policy initiatives across the pharma and biotech CMC and Regulatory CMC topics.

You will either be:-

  • With an Agency / Regulator in a Pharmaceutical Assessor or a related role, and have taken part in policy drafting or have direct experience in outreach to sponsor side companies and trade associations on new CMC related regulatory guidelines and instruments OR
  • You are currently in a major Trade Association and manage the CMC / RA CMC topics
  • You are working in a similar role with a biotech or pharma and now feel ready to build a new footprint for a company with several successful biotech and small molecule products, each a blockbuster in their own right!

Package & Benefits

Firstly, my client is willing for compelling individuals to buy out stock within reason. Secondly, the role comes with a high-end package including bonus, RSU based stock, and in certain countries a car or car allowance. The company have bandwidth on grading for formidable applicants with a clear track record in shaping CMC and CMC regulatory policy.

Relocation / Location & Covid

This role will be based in central London or from the EU head office in the South-East / M4 corridor within easy reach of London and Heathrow or from Oxford and surround counties such as Surrey, Hampshire, Berkshire, Buckinghamshire.

Covid 19: My client has a digital hiring and on-boarding process and can hire / on-board you from home if Covid continues. Afterwards, office working is normal, but this role will require some travel for both internal stakeholder and external association and policy forum meetings.
 

To Apply!

To apply, please send a full CV to CV@AdvTalent.com, or alternatively contact either myself Theo Moore on +44 (0)207 801 3384, or my colleague Matt Greig - takes calls on Saturday and Sunday AMs (US and European times) on +44 (0)207 801 3386 or mobile+44 7918 679 405.

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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