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Michael Jones graduated from KGI in 2019 with a concentration in Pharmaceutical Discovery & Development through the MBS program. He has participated in a 2-year Regulatory Affairs Rotational program at Gilead Sciences where he explored the Regulatory Documentation and Submission processes, R&D Quality and Compliance, Regulatory Liaison and Regulatory Policy & Intelligence roles. He is currently a Senior Associate in the Disclosure and Transparency team within R&D Quality and Medical Governance. In this role, he is responsible for ensuring any documents submitted to the public through global health authorities protect Gilead’s Intellectual Property and personal patient data. He is also responsible for the management and improvement of Gilead’s public clinical trial website.
Discussion Topic: Regulatory Affairs