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The Programme




  • Develops individual protocols and data analysis plans and determines appropriate statistical methodology for data analysis
  • Participates in database design meetings to ensure that the data evaluated are in high quality and satisfy analysis requirements
  • Collaborates with the statistical programming staff to ensure that all programs meet analysis requirements, internal standard operating procedures, and external regulatory requirements
  • Analyzes data and interprets results from clinical trials to meet objectives of the study protocol. Applies and implements basic and complex techniques to these analyses under supervision
  • Prepares oral and written reports to effectively communicate results of clinical trials to the project team
  • Provides responses to queries relating to study design, analysis, and interpretation posed by the clinical monitors, regulatory agencies, and/or investigators
  • Participates with management in discussions with corresponding scientific personnel at regulatory agencies and with investigators concerning proposed or ongoing studies
  • Involved in research activities for innovative statistical methods and applications in clinical trial development

Required Skills and Abilities

  • PhD or equivalent degree in statistics/biostatistics or related discipline
  • Knowledge of statistical analysis methodologies and experimental design
  • Working knowledge of statistical and data processing software e.g. SAS and/or R
Closed a year ago
Closed a year ago
  • Job type:Graduate Jobs
  • Disciplines:


  • Citizenships:

  • Locations:

    Beijing (China)

  • Closing Date:21st Mar 2019, 6:00 pm


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