I offer advice in the following fields of drug development:
* Choice of design
* Sample size estimation
* Protocol writing
* CRF design
* Statistical analysis plans
* Design of tables, listings and graphs
* Specifications of analysis datasets
* Programming and validation
* Data monitoring
* Preparation of (blind) data review
* Key results memos
* Clinical study reports
* Publications
* Support during drug submission
* Meta-analysis
* Support of IDMCs (independent data monitoring committees)
* Statistical training