HLX Life Sciences is seeking a Senior Manager, Regulatory Affairs (Europe) to own a small portfolio from strategy and submission through to approval and lifecycle, reporting to the Associate Director, Regulatory Affairs. The role is hybrid in the UK and permanent, full-time.
You will lead centralised MAAs to EMA and MHRA submissions, set regulatory strategy, prepare pediatric investigation plans and guide lifecycle maintenance, with responsibility for mentoring less experienced team members.
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European Regulatory Affairs Lead — MAA, EMA/MHRA employer: Hlx Life Sciences
As a leading CRO, we pride ourselves on fostering a collaborative and dynamic work environment that empowers our Clinical Research Associates to thrive. With a focus on global clinical trials, we offer unique opportunities for professional growth and development, particularly for those fluent in French and English, while supporting a diverse range of therapeutic areas. Our commitment to employee well-being and flexible working arrangements ensures that you can balance your career with personal commitments, making us an excellent employer for those seeking meaningful and rewarding work in the UK.
