Lesley-Anne Chapman

Lesley-Anne Chapman currently serves as the Manager of Regulatory Submissions Planning at PTC Therapeutics, Inc., a position held since February 2023. Prior experience includes managerial roles in regulatory publishing and operations at Voisin Consulting Life Sciences from September 2021 to February 2023 and as a Principal Submission Consultant at DLRC Regulatory Consultancy from June 2020 to September 2021. Lesley-Anne held the position of Global Regulatory Operations Manager at Celgene and served as Global Submission Manager at PRA Health Sciences before taking a career break to care for a family member from July 2017 to June 2018. Previous significant roles include Associate Director of Submission Sciences and Senior Manager at Biogen, as well as a Senior Consultant at Liquent Ltd. Lesley-Anne's career began at Pfizer, where responsibilities included the role of Senior Associate. Expertise encompasses leading project teams, ensuring the quality and timeliness of regulatory submissions in compliance with agency guidelines.