Location: San Francisco, CA



  • Provides statistical input into Phase I – IV clinical trial development
  • Designs and analyzes clinical trials
  • Maintains the statistical and analytical integrity of clinical trials analyzed
  • Participates in writing statistical sections of protocols, preparing statistical analysis plans, preparing data deliverables for clinical study reports and interpreting statistical results for clinical study reports
  • Participate in the development of protocol, study design, SAP, ISS/ISE and analysis dataset specifications
  • Working with programmers to perform statistical based on timelines defined by the company


  • BA degree in Computer Science, Mathematics, Statistics and related areas is required
  • Masters or PhD is preferred
  • Equivalent experience may be accepted
  • Minimum of 12 years relevant career experience in the pharmaceutical or biotechnology industry