8 month contract

The SAS Programmer will
provide statistical programming of derived datasets, analyses, tabulations,
graphics, and listings from clinical trial data. You will also be required to
perform quality control procedures on work performed by others.  You must have experience in the
pharmaceutical/Biotech industry working through Phases I - III clinical trials
providing outputs for Clinical Study Reports and integrated summaries for
submission to regulatory agencies. 
Requirements include strong SAS programming skills with 10+ years
clinical trial statistical programming experience, strong knowledge of SAS
report writing and SAS Macro language, good verbal and written communication
skills, enabling effective participation in cross-functional team environment,
and experience working in a Unix environment.