Julie Eng Lee
About Julie Eng Lee
Julie Eng Lee is a Senior Manager at Bristol Myers Squibb, specializing in Clinical Trial Systems & Quality Auditing, with over a decade of experience in clinical quality assurance and compliance.
Current Position at Bristol Myers Squibb
Julie Eng Lee currently holds the position of Senior Manager, Clinical Trial Systems & Quality Auditing at Bristol Myers Squibb. She has been with the company since November 2019, and is based in Summit, New Jersey, United States. Her role involves overseeing clinical trial systems and ensuring compliance with quality auditing standards.
Previous Roles at Celgene
Julie Eng Lee's professional journey includes extensive experience at Celgene, where she worked from 2009 to 2019. She progressed through several roles: Computer System Validation Auditor (2009-2011), Associate Auditor, Clinical Quality Assurance & Compliance (2011-2014), GCP Auditor (2014-2016), Manager, Clinical Quality Assurance (2016-2017), and Sr. Manager Clinical Quality Assurance (2017-2019). Her work at Celgene consistently involved quality assurance and compliance in clinical settings, contributing to a decade-long tenure at the company.
Experience as a Business Analyst at Eisai US
Before joining Celgene, Julie Eng Lee served as a Business Analyst, eDMS, at Eisai US from 2007 to 2009. Based in Ridgefield Park, New Jersey, she contributed to the electronic document management systems (eDMS) during her two-year tenure, supporting the company's document management and operational processes.
Education at Fairleigh Dickinson University
Julie Eng Lee completed her undergraduate studies at Fairleigh Dickinson University from 2000 to 2004. The specifics of her degree are not provided, but her education laid the foundation for a career in clinical quality assurance and compliance.
Expertise in Clinical Quality Assurance and Compliance
With over a decade of experience in clinical quality assurance and compliance, Julie Eng Lee has established expertise in managing clinical trial systems, quality auditing, and ensuring regulatory compliance. Her professional background includes roles focused on computer system validation auditing and quality process management in pharmaceutical companies. This extensive experience has equipped her with a comprehensive understanding of the clinical quality assurance landscape.