Rosalind McCully is an experienced regulatory affairs professional with extensive expertise in chemistry, manufacturing, and compliance (CMC) regulatory leadership. Currently serving as Associate Director and CMC Global Regulatory Lead at Biogen since March 2022, Rosalind manages major marketing authorization applications and lifecycle management changes for new active substances. Prior to this role, Rosalind held various positions at IQVIA, PAREXEL Consulting, and AstraZeneca, focusing on strategic partnerships, project management, and regulatory submissions. With a Ph.D. in Pharmacy/Medicine from Cardiff University and a foundation in pharmacology from University of Strathclyde, Rosalind's career also includes experience as a pharmaceutical assessor in Malaysia and a pre-registration pharmacist in a leading public hospital.
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