Description
Performs all SAS programming required for clinical trial analysis and reporting- Ensures that activities and processes performed are conducted according to sponsor requirements
- Works closely with the Biostatistics and Data Management departments on various clinical projects
- Leads programming efforts for large complex studies
- Reviews case report form design
- Designs and/or reviews database structure
- Writes edit checks from the Data Cleaning Plan specifications
- Creates derived-analysis datasets
- Executes analyses specified in the Statistical Analysis Plan or Report and Analysis Plans under the guidance of the project statistician
- Acts as primary programmer to produce tables, listings, and figures for the clinical study report
- Acts as secondary programmer to validate SAS programs that produce derived-analysis datasets and data analyses
Requires time management skills, and strong SAS programming expertise. Intermediate MS Word desired.