Experience

Luye Pharma Group

• China
• Pharmaceutical Manufacturing
• 100 - 200 Employee

• Associate Director Biostatistics

  • Feb 2018 - Present



Salubris Pharmaceuticals

• China
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Associate Director of Data Operation

  • Jun 2017 - Jan 2018



Parexel

• United States
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Associate Manager, Statistical Programming

  • Apr 2015 - May 2017

  Responsibilities include providing a broad range of leadership and team building capabilities to manage the performance and development of a statistical programming team in order to achieve departmental goals and objectives, conducting performance appraisals, managing the annual salary planning for a statistical programming team in line with other statistical programming managers and directors, contributing to and implement a strategy for the structure and development of a statistical programming team, resource planning, including monitoring and scheduling the workload of a statistical programming team, managing the recruitment process for new statistical team members, evaluating and resolving complex personnel issues, implementing disciplinary procedures if required, providing support to project leads to help manage changes in scope and contractual issues, proactively participating in and/or lead process/quality improvement initiatives, communicating with other operational groups regarding workflow, process, timelines, and resource planning to ensure transparency between all functions as well as any external support groups, providing technical leadership, and project management for required technical aspects supporting clinical trial activities, Consistency checks, analysis dataset and table, figure and listing programming and any ad-hoc programming required to support a clinical trial process, identifying and adequately resolving operational and technical problems, working closely with the Quality, Process and Training Groups to ensure compliance with WSOPs/Guidelines, leading cross functional meetings and drive initiatives to ensure the delivery of milestones and timelines for clinical trials, providing relevant technical training and/or mentoring for staff to assist them in resolution of problems encountered in the conduct of their daily work, presenting statistical programming at internal and external audits and regulatory inspections.



GCP CMIC ClinPlus Co.,LTD

• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Senior-statistician

  • Aug 2008 - Mar 2015

  SAP, SAR, SIMPLE SIZE CALCULATE, SAS PROGRAM, SDTM, ADAM