Allucent is seeking a Director of Regulatory Affairs to guide clients through drug, biologic and medical device development. You will lead regulatory teams, shape strategies, and ensure high-quality submissions while Interacting with Health Authorities globally.
The role includes SME duties, technical leadership, and cross-functional collaboration across project teams to deliver impactful regulatory outcomes.
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Director, Regulatory Affairs — Global Submissions Leader in London employer: Allucent
Allucent is an exceptional employer that prioritises employee well-being and professional growth, offering a flexible remote or hybrid working environment tailored to the needs of our team. With a strong commitment to compliance and data quality in clinical programming, we provide comprehensive benefits and opportunities for career advancement, making it a rewarding place for those passionate about drug development.
