Biostatistician Coordinator

11 - 15 years

Posted 267 days ago

This job is no longer available.


  • Assist in implementing infrastructure for the discipline of biostatistics and statistical programming for FDA regulated clinical studies in human subjects
  • Assist with oversight of activities and create, maintain, and oversee project schedules and deliverables
  • Maintain quality control and versions for biostatistics and Statistical Analysis System (SAS) programming SOP’s
  • Provide quality control review (validation), formatting, and version control of statistical programming output, biostatistical deliverables and documents
  • Manage documentation and validation activities surrounding statistical programming 
  • Participate in team meetings and prepare agendas and minutes
  • Maintain document control of biostatistics materials in the FDA regulated document management system


  • Knowledge of biostatistics and ability to develop correspondence and various documents in compliance with SOPs, using correct grammar, punctuation, and spelling
  • Education and training on clinical biostatistics and statistical programming, SOPs, templates, and forms

MINIMUM EDUCATION: Minimum of an Associate’s degree with more than 10 years of directly related experience.