Provide statistical consulting to clinical study design; Review study protocols and write statistical sections; Conduct sample size and power calculations; Propose randomization methods and designs; Generate randomization schedules; Assist in regulatory submission strategy planning; Participate in study team operations and timeline discussion; Identify issues, and provide solutions to clinical operation and data management for issues that potentially impact data analyses
Requirements:
Master’s or Doctoral degree in statistics or biostatistics; Master’s degree with 4-8 years or Doctoral degree with 2-6 years of relevant experience in a health sciences research institute or the pharmaceutical/biotech industry
Text:
Senior Statistician Provide statistical consulting to clinical study design; Review study protocols and write statistical sections; Conduct sample size and power calculations; Propose randomization methods and designs; Generate randomization schedules; Assist in regulatory submission strategy planning; Participate in study team operations and timeline discussion; Identify issues, and provide solutions to clinical operation and data management for issues that potentially impact data analyses Master’s or Doctoral degree in statistics or biostatistics; Master’s degree with 4-8 years or Doctoral degree with 2-6 years of relevant experience in a health sciences research institute or the pharmaceutical/biotech industry
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