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上海, 臨床及註冊 | 2021-10-04

Senior Statistician

Job Title: Senior Statistician
Location: Shanghai


Primary Function

The Senior statistician is responsible for all statistical aspects of a clinical development project of one compound, from early clinical development, to registration and marketed product support.


  • Serves as statistical representative in the cross-functional teams for the strategic planning, execution for product development and trial design.
  • Involved in research activities for innovative statistical methods and applications in clinical trial development.
  • Prepare statistical related sections in clinical trial protocols, clinical trial reports, submission documents, and publications.
  • Develops statistical analysis plans (SAP) or oversees SAP development.
  • Oversees trial conducts from statistical perspective.
  • Assist with or be responsible for communicating study results via regulatory submissions, manuscripts, or oral presentations.
  • Oversees process and quality of statistical work contracted out to a CRO or research collaborator.
  • Performing statistical programming to validate the results produced by CRO or to meet internal need of data analysis (e.g. for publication, or for optimizing assumptions for study design), when needed.
  • Mentors junior colleagues in techniques, processes.



  • PhD degree in statistics/biostatistics or related discipline with a minimum of 2 years work experience as statistician in pharma/CRO, or a Master’s degree with a minimum of 4 years work experience as statistician in pharma/CRO.
  • Thorough knowledge of statistical methodology, pharmaceutical research and development strategies and execution, GCP and regulatory guidelines.
  • Good project management skills
  • Excellent communication and presentation skills to interact with authorities and external bodies (specialists as well as non-specialists) on statistical-methodological issues
  • Strong time management and prioritization skills
  • Knowledge of statistical tools such as SAS, nQuery, PASS, East
  • Demonstrate strong interest in statistical research activities and in application of novel methods to clinical trial development.

If interested, please forward your resume to