Expiry Date: 18-10-2021
Categories Biotech, Pharmacy, Regulatory Affairs
Salary: On Application
Job Type: Full Time
Global Regulatory Strategy Lead – Early Dev – Bucks / Beds / Herts
My colleagues and I are recruiting for a Global Regulatory Affairs Director or upper level Associate Director to lead projects in development for an international bio-pharmaceutical company based in the UK.
Our client is a European-led, global bio-/pharmaceutical company with a history dating back well over 70 years in CNS & Neurology. The function is led by a very well-known Head, and the team is global, including US and EU, managed by an equally capable Senior Director, with a track record in gaining approvals, this role reports in to this person.
This is a permanent role for an experienced Regulatory Affairs Strategist for development projects in Neurology, leading submissions for novel compounds (NCEs / NBEs) – often with adaptive pathways and multiple indications including rare diseases.
The culture is science based, this role will matrix report into a Dev Lead (PL), naturally, this means the team is R&D focused, with an eye to assisting the commercialization team with novel or RWE or PRO end-points, to gain the right data for both the regulatory approval and market access. Also the company respect work life balance, and are known for working smart. It’s a smaller company so getting stuff done is somewhat easier, and stakeholders are driven on data, not personality.
In return, it is essential to have at least 7-12 years of Regulatory Affairs regional or global strategy experience, a strategic mind-set and the ability to create and innovative regulatory strategy.
You will have a proven track record of leading major Health Authority interactions and submissions, in either early development or late phase to filing.
English is the business language in the company.
To apply for this role, please press the red “Apply for position” button, or contact Oli Dimitrov on +44 (0)207 801 3388 or Matt Greig on +447918679405 in full confidence to receive more details on this role or to hear about other available opportunities in Regulatory Affairs.
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