Caitlin Bergeron

Caitlin Bergeron is an experienced regulatory affairs professional currently serving as a Senior Manager of Regulatory Affairs at Neumora since January 2024. Previously, Caitlin held a similar role at EQRx from June 2021 to August 2023 and served as a Regulatory Affairs Manager and Specialist at Akebia Therapeutics from August 2016 to June 2021. Caitlin's regulatory expertise includes preparing and maintaining submission tracking logs, compiling documentation for regulatory submissions, and reviewing documents for compliance and accuracy. Earlier experience as a Regulatory Affairs Specialist was gained at Medivector Inc. and as a Quality Control Technician and Reagent Manufacturing Technician at Siemens Healthcare Diagnostics contributed to a strong foundation in quality assurance and regulatory compliance. Caitlin's educational qualifications include a Master of Science in Regulatory and Clinical Research Management from Regis College and a Bachelor of Science in Biology from Stonehill College.