Sophie Mukadam

Sophie Mukadam is an experienced professional in the pharmaceutical industry, currently serving as Associate Director of Program Management at Benitec Biopharma Inc. since May 2019. Prior roles include Senior Program Manager and Regulatory Affairs Associate at Regulatory Professionals, Inc., and a Regulatory Consultant at Henlix, Inc., where expertise in filing INDs for large molecules was developed. Sophie has also contributed to Genentech, Inc. as a Senior Research Associate in Drug Metabolism and Pharmacokinetics, with extensive experience in PBPK modeling and DDI risk assessment. With a foundation in molecular and cell biology from the University of California, Berkeley, and a Certificate in Project Management for Biotechnology from the University of Washington and UCSD, Sophie Mukadam combines strong scientific knowledge with program management skills.