I offer advice in the following fields of drug development:

Clinical trial design:

  • Choice of design
  • Sample size estimation
  • Protocol writing
  • CRF design

Data analysis:

  • Statistical analysis plans
  • Design of tables, listings and graphs
  • Specifications of analysis datasets
  • Programming and validation
  • Data monitoring
  • Preparation of (blind) data review

Presentation and interpretation of results:

  • Key results memos
  • Clinical study reports
  • Publications

Other statistical consultancy, e.g.:

  • Support during drug submission
  • Meta-analysis
  • Support of IDMCs (independent data monitoring committees)
  • Statistical training