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