Performs data analysis using primarily the SAS programming language for the summary and interpretation of clinical trial data.
? Creates CDISC SDTM and ADaM files, SAS export files and Define.xml use for Electronic Submission from the data received in non-standard form from various sources.
? Performs Data analysis, statistical analysis, generate safety and efficacy tables, listings and graphs using Base SAS, SAS Macros, SAS/STAT, SAS/Graph, SAS/SQL and SAS/ODS.
? Reviews Data Management Plan, Data validation plan and edit check specifications