Lianqi Lindsey Xie
About Lianqi Lindsey Xie
Lianqi Lindsey Xie is a Senior Manager of Statistical Programming at Kite Pharma, with extensive experience in statistical programming and clinical trial data management. She has worked at several prominent organizations, including Gilead Sciences and The Medicines Company, and possesses strong skills in project management, SAS programming, and regulatory compliance.
Work at Kite Pharma
Lianqi Lindsey Xie currently serves as the Sr. Manager of Statistical Programming at Kite Pharma, a position held since 2018. In this role, Xie is responsible for overseeing statistical programming activities, ensuring compliance with regulatory standards, and managing project timelines. The position requires a strong understanding of clinical trial data management and reporting, which aligns with Xie's extensive background in the field.
Previous Experience in Statistical Programming
Prior to joining Kite Pharma, Xie worked at Gilead Sciences in various roles, including Sr. Statistical Programmer and Associate Manager of Statistical Programming from 2013 to 2018. Xie's experience also includes positions at United Biosource Co. as a Senior Clinical Programmer/Analyst I and at The Medicines Company as a Statistical Consultant. This diverse background has equipped Xie with a comprehensive understanding of statistical programming within clinical trials.
Education and Expertise
Xie earned a Master's degree from The University of Georgia, where studies focused on biostatistics and statistical analysis. This educational foundation has been instrumental in developing Xie's expertise in missing data simulation and imputation, SAS programming, and adherence to CDISC data standards such as SDTM and ADaM. Xie's strong educational background supports a robust skill set in statistical analysis and project management.
Background in Clinical Trials
Xie has a solid background in clinical trials, having worked in various capacities across multiple organizations. This includes significant experience in managing project timelines and resources, which is critical for the successful execution of clinical studies. Xie's ability to conduct ad hoc analysis and data mining enhances the capacity to derive insights from complex clinical trial data, contributing to informed decision-making.
Regulatory Knowledge and Global Collaboration
Xie possesses extensive experience in handling NDA filing and regulatory responses, indicating a strong understanding of the pharmaceutical regulatory landscape. Additionally, Xie's work in a global environment demonstrates the ability to collaborate and communicate effectively across diverse teams and functions, which is essential in the pharmaceutical industry.