Authoring statistical analysis plan (SAP) and shells for Phase I - IV clinical trials.  
Providing statistical programming service for Phase I - IV for biotech, pharma, or academic clinical studies.
Creating and validating SAS programs and macros for SDTM and ADaM data sets,  tables, listings, and figures.
Authoring SDTM and ADaM specifications.
Providing consultation on CDSIC SDTM and ADaM standards.
Implementing  CDISC SDTM and ADaM standards. 
Reviewing submission packages.
Creating SDTM Define files (xml and pdf).
Creating ADaM Define files (Define.xml and Define.pdf version 1.0 or Define.xml version 2.0).
Providing CDISC SDTM, ADaM, Define-xml training.