Associate Director, Regulatory Affairs
Claire is a CMC regulatory affairs professional with more than 20 years’ experience in the pharmaceutical industry and an extensive background in biological and inhalation product development. She has a successful track record in delivering CMC regulatory strategies and submissions for development and marketed products, and joined Boyds’ Regulatory Affairs team in April 2019.
Claire previously worked at Mundipharma where she was a Regulatory Affairs Senior Manager in CMC and Compliance. She was the lead for a diverse range of development and marketed products including new chemical entities and biologics, and authored and reviewed high-quality CMC documentation (M3 and M2.3) for submission in Europe and Rest of World territories.
Prior to this, Claire was at Pfizer for 13 years, starting as a Biologics Liquid Formulation Scientist before progressing to an Inhalation Formulation Senior Scientist and then a Principal Scientist for the Device Centre of Emphasis.
Claire has a first-class honours degree in BPharm from the University of Nottingham and is a member of the General Pharmaceutical Council, the Royal Pharmaceutical Society and TOPRA.
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