Helene Chau

Helene Chau

Project Coordinator @ Bristol Myers Squibb

About Helene Chau

Helene Chau is a Project Coordinator at Bristol-Myers Squibb with over 15 years of experience in the clinical research and pharmaceutical industry.

Current Role at Bristol-Myers Squibb

Helene Chau currently holds the position of Project Coordinator at Bristol-Myers Squibb. In this role, she is responsible for overseeing project logistics and ensuring the smooth execution of clinical trials. With over six years at the company, she brings a wealth of experience and expertise to the position, contributing to the advancement of clinical research.

Previous Experience at Inventiv Health Clinical

Before her current role, Helene Chau worked at Inventiv Health Clinical, initially as a Business Operations Analyst and Senior Clinical Trial Associate (CTA) for Bristol-Myers Squibb in 2016. She was in this position for eight months. Prior to this, she was a Senior Clinical Trial Associate outsourced to Bristol-Myers Squibb from 2015 to 2016, for a duration of nine months.

Experience at IQVIA

Helene Chau’s tenure at IQVIA lasted from 2011 to 2015. She served as a Senior Clinical Trial Assistant for three years, from 2012 to 2015. Additionally, she worked as a Clinical Trial Assistant and In-house CRA from 2011 to 2012, which gave her foundational experience in clinical trial management.

Early Career at Clearstone Central Laboratories

Helene Chau began her professional journey at Clearstone Central Laboratories, where she held the role of Customer Support Coordinator from 2008 to 2010. This early experience in customer support provided her with the essential skills needed to transition into clinical trial roles in the pharmaceutical industry.

Extensive Experience in Clinical Research and Pharmaceuticals

Helene Chau has amassed over 15 years of experience in the clinical research and pharmaceutical industry. Her extensive background includes significant roles at major companies like Bristol-Myers Squibb and IQVIA. Throughout her career, she has developed a robust skill set in clinical trial management and coordination, making her a valuable asset in her current capacity.

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