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; Lead regulatory submission strategy planning for statistics function; Identify issues, and provide solutions to clinical operation and data management for issues that potentially impact data analyses; Review and provide comments to statistical analysis plans that are written by the 3rd party
Requirements:
Master’s degree with 6-10 years or Doctoral degree with 4-8 years of relevant experience in a health sciences research institute or the pharmaceutical/biotech industry; Direct participation in design, planning, conduct, analyses, and reporting of clinical trials; Direct participation in regulatory submission activities
Text:
Principal 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; Lead regulatory submission strategy planning for statistics function; Identify issues, and provide solutions to clinical operation and data management for issues that potentially impact data analyses; Review and provide comments to statistical analysis plans that are written by the 3rd party Master’s degree with 6-10 years or Doctoral degree with 4-8 years of relevant experience in a health sciences research institute or the pharmaceutical/biotech industry; Direct participation in design, planning, conduct, analyses, and reporting of clinical trials; Direct participation in regulatory submission activities
Please click here, if the job didn't load correctly.
Please wait. You are being redirected to the job in 3 seconds.
