Responsible for primary and validation programming for CDISC - SDTM conversion and responsible for validation of CRTs.

Responsible for providing all required SAS programming functions

Responsible for working with project statistician to design tables, listings, graphs and statistical summaries

Responsible for coordinating all programming activities for assigned projects

Develop macros for statistical analysis

Generate statistical analysis files, tables, listings, and graphs for clinical trial studies

Provide support on interpretation and implementation of Statistical Analysis Plan(s) (SAP)

Review and comment on client SAS Programming Specifications and SAS code

Creation and maintenance of documented SAS coding standards Oversee the archival of final approved versions of SAS programs generated by clients and internal staff

Mentor and train Jr.SAS programmers/ Statisticians/ Biostatisticians Importing and exporting data

Finding the data issues while creating data listings