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