Our biostatisticians have the expertise to support your needs in clinical study protocol development, statistical planning and data review, statistical analysis, and statistical report preparation. Our statistical programmers are experts at SAS programming, including production report programming and program validation.
Clinical Study Protocol Development
- Development of study design
- Sample size/power determination
- Formulation of statistical analyses
- Write statistical analysis section of protocols
Statistical Planning and Data Review
- Write statistical analysis plan detailing statistical methodologies
- Write detailed descriptions of data consistency checks
- Write detailed descriptions of data listings
- Write detailed descriptions of tables and graphs
- Review data for sample size/statistical problems Statistical Programming (SAS)
- Program data consistency checks
- Program data listings
- Program tables and graphs
- Convert data to SAS format
- Statistical analyses programming
- Program validation
Statistical Analysis
- Perform interim and final statistical analysis of clinical study data
- Perform statistical analysis for integrated study reports
- Consult on statistical problems Statistical Report Preparation
- Prepare statistical report
- Write statistical sections of clinical study reports
- Write statistical sections of integrated study reports