Statistical Analysis

• Develop randomization schemes
• Develop sample selection for observational studies
• Develop interim and final analysis plans
• Create tables, files, and listings for FDA submissions
• Provide expertise regarding methdological issues in statistics
• Perform analyses for manuscripts and interim reports

We use in-house statisticians and statistical programmers to support statistical design and analysis. We can also draw from a wealth of expertise within UCSF and the CPMC Research Institute, as needed. Our statistical programmers have created a suite of validated SAS programs and macros that can be customized for reports, tables, and listings for regulatory submissions and data safety reporting.

Manuscripts and Presentations

• Assist in creating presentations and developing manuscripts for publication
• Establish publication review systems
• Coordinate study-wide analysis for publications involving multiple investigators

Coordinating Center scientists have published in high-impact journals such as NEJM and JAMA.