Xiangyang Yue
About Xiangyang Yue
Xiangyang Yue is the Site Monitor Manager at 百时美施贵宝 in Beijing, with over a decade of experience in site monitoring and management.
Current Title and Role
Xiangyang Yue serves as the Site Monitor Manager at 百时美施贵宝 in Beijing. In this role, Xiangyang is responsible for overseeing site monitoring activities, ensuring compliance with regulatory requirements, and managing site staff. With over a decade of experience in the field, Xiangyang brings substantial expertise to the position, fostering efficient site operations within the pharmaceutical industry.
Professional Experience at PAREXEL
Xiangyang Yue began his career in clinical research as a Clinical Research Associate at PAREXEL. He worked there from 2010 to 2012, during which time he developed foundational skills in clinical trial monitoring and site management. His responsibilities included coordination and oversight of clinical trials, ensuring protocol adherence, and liaising with site personnel in Beijing City, China.
Education and Academic Background
Xiangyang Yue holds a Master's degree in Pharmaceutical Analysis from Shandong University, where he studied from 2007 to 2010. Prior to this, he achieved a Bachelor's degree in Pharmacy from Sichuan University, completing his studies from 2003 to 2007. This strong academic background in pharmaceuticals provides a solid foundation for his extensive work in clinical research and site management.
Long-Term Commitment and Stability
Xiangyang Yue has been with 百时美施贵宝 for over 11 years, demonstrating a high level of commitment and stability in his role. His long-term tenure is a testament to his dedication and reliability, contributing to sustained success and consistency in site monitoring and management operations.
Expertise in Site Monitoring and Management
With over a decade of experience in site monitoring and management, Xiangyang Yue possesses extensive knowledge of clinical research processes. His expertise encompasses regulatory compliance, site operations, and coordination of clinical trials, making him a valuable asset in the pharmaceutical industry. Xiangyang’s combined academic knowledge and practical experience enable him to efficiently oversee site activities and ensure successful trial outcomes.