Aaron Corona

Aaron Corona has extensive work experience in the pharmaceutical industry. Aaron started their career at Xenogen Corporation in 2003 as a Research Scientist. In 2006, they joined Merck, where they held multiple roles, including Scientist, Biologist, Global Project Manager, and Regulatory Submissions Project Manager. Their responsibilities at Merck included managing global regulatory submissions, developing regulatory strategies, and coordinating cross-functional program activities. In 2017, they joined Amicus Therapeutics as a Project Manager in Regulatory Affairs and later progressed to the role of Director of Project and Submissions Management in Global Regulatory Affairs. Currently, they serve as the Senior Director of Regulatory Operations at Amicus Therapeutics.

Aaron Corona attended Rutgers University from 1999 to 2003, where they obtained a Bachelor of Science degree in Animal Science. In addition, they obtained certifications in Vault RIM - Business Administrator from Veeva Systems in 2021 and Project Management Professional (PMP) from the Project Management Institute in 2011.