Xiaolei Zhang
About Xiaolei Zhang
Xiaolei Zhang is a Senior Manager in Statistical Programming at Bristol Myers Squibb with extensive experience in the pharmaceutical industry and expertise in clinical data design and regulatory submissions.
Title
Xiaolei Zhang is a Senior Manager, Statistical Programming at Bristol Myers Squibb. He brings a wealth of experience and expertise to his current role in statistical programming and project management within the pharmaceutical industry.
Professional Experience at Bristol Myers Squibb
As the Senior Manager of Statistical Programming at Bristol Myers Squibb, Xiaolei Zhang leads a team of experts in the development and implementation of sophisticated statistical models and data analysis methodologies. His role involves regulatory submission activities and responding to regulatory queries, ensuring compliance with industry standards.
Previous Roles and Responsibilities
Xiaolei Zhang has accumulated diverse experience in statistical programming and analysis through his previous roles. At Eli Lilly and Company, he served as a Cnslt Statistician for six years, where he focused on clinical data design and statistical analysis. Prior to that, he worked as a Sr Statistical Programmer at inVentiv Health for five years and as an Associate Scientist at Amgen for five months. Early in his career, Zhang held teaching positions at Texas Tech University and worked as a Data Analyst at the University of Washington.
Education and Expertise
Xiaolei Zhang holds a Master of Science in Statistics from Texas Tech University and a Bachelor of Science in Applied Mathematics from Donghua University. He is proficient in advanced statistical programming languages and tools, including SAS, SAS/SQL, SAS Macros, SAS GRAPH, Spotfire, and R. His expertise extends to additional programming and analytical tools such as SPLUS, MATLAB, SPSS, C, C++, Excel, NONMEM, WinNonLin, and Python.
Skills and Technical Proficiency
Xiaolei Zhang has a strong background in statistical modeling and statistical analysis for clinical trials. He is experienced in working with submission standards such as CDISC (SDTM, ADaM), Define.XML, SDRG, and ADRG. His skill set includes project management, clinical data design, and methodologies, demonstrating excellent interpersonal and multi-tasking abilities with a proven capacity to negotiate and collaborate effectively.