A pioneering biotech focused on individualized therapies for rare pediatric neurodegenerative conditions is seeking a Senior Vice President / Vice President of Regulatory Affairs. This executive role will lead global regulatory strategy, with a particular focus on the UK and EU, supporting the development of advanced genetic therapies using ASO technologies.
This company is transforming the treatment landscape for children with devastating, life-limiting neurological diseases—offering an opportunity to directly impact the lives of patients and families with few, if any, existing therapeutic options.
Lead regulatory strategy and submissions across the UK, EU, and potentially the US
Liaise with MHRA, EMA, and other authorities to ensure regulatory alignment
Advise internal stakeholders on regulatory risks and compliance
Represent the company in external regulatory forums and industry groups
Scale regulatory operations during rapid organizational growth
15+ years’ experience in regulatory affairs within pharma/biotech, with significant experience in paediatric and rare disease programmes
~ Proven leadership in EU/UK submissions and regulatory agency engagement
~ Advanced degree (PhD, PharmD, or MSc) in a scientific discipline
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