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Catherine Sherwin has 18 years of experience in clinical pharmacology and toxicology, with a focus on pharmacometrics and clinical trials specializing in pediatric and maternal-fetal pharmacology. She has expertise in population pharmacokinetics and optimal trial design. Her academic career spans 15 years in institutions across the USA, where she has held roles such as Professor of Pediatrics and Pharmacology/Toxicology, and Vice Chair of Research, demonstrating leadership in clinical trial operations for over eight years and directing a Clinical Research Centre for five years. Additionally, she works as an independent consultant in clinical pharmacology and modeling/simulation. Sherwin is a Fellow of the American College of Clinical Pharmacology and a Diplomate of the American Board of Clinical Pharmacology, certified as a Principal Investigator by the Association of Clinical Research Professionals. She earned her PhD in Paediatric Clinical Pharmacology from the University of Otago, Dunedin School of Medicine, New Zealand, and her MPharm in Clinical Toxicology from the University of Florida.
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