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CG Leong has extensive experience in the field of Quality Assurance in the clinical research industry. They started their career at Johnson & Johnson as a Program Manager from 2009 to 2013. Following that, they joined GlaxoSmithKline as a Regional Manager, overseeing Clinical Development Quality Assurance from 2013 to 2019. CG then worked at Amgen as the JAPAC GCP/GLP Compliance Lead from 2019 to 2021. They subsequently joined argenx as an AP Quality Lead, responsible for inspection readiness, management, and vendor audit qualification within the Asia Pacific region. In addition, CG provided GCP consulting advice, ensuring quality oversight from study design to completion. Currently, CG Leong holds the position of Head of Global Clinical QA at Evive Biotech, where they lead the team in providing independence quality audits, maintaining inspection readiness, and supporting inspections from external and health authorities.

CG Leong attended SMJK Nan Hwa from 1989 to 1994, where they earned their GCE O Level. CG later enrolled at Middlesex University from 1997 to 1998, where they pursued a Bachelor of Science (BSc) degree in Information Technology with a focus on Business Information Systems.