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Uk regulatory affairs lead — maa submissions & strategy

Gatwick
Novo Nordisk
€70,000 a year
Posted: 2 March
Offer description

A global healthcare company is seeking a Regulatory Affairs Lead in Gatwick, UK. This role involves managing and executing regulatory projects, providing strategic support, and collaborating across functions to align regulatory submissions with business needs. Candidates should have at least 8-10 years of experience in a regulatory environment, possess extensive knowledge of UK and EU legislation, and demonstrate strong stakeholder management skills. The position offers the opportunity to make a direct impact on patient health while working in a collaborative team environment.
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