SAS Programmer III

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. Requires time management
skills, and strong SAS programming expertise. Reviews case report form
(CRF) design. Designs and/or reviews database structure. Writes edit
checks from the Data Cleaning Plan (DCP) specifications. Creates
derived-analysis datasets. Executes analyses specified in the
Statistical Analysis Plan (SAP) or Report and Analysis Plans (RAP) under
the guidance of the project statistician. Acts as primary programmer to
produce tables, listings, and figures for the clinical study report
(CSR). Acts as secondary programmer to validate SAS programs that
produce derived-analysis datasets and data analyses. Years of Experience
5-7.

$79/hr

18 months