Responsible for performing analyses on clinical trial data, including listings, tabulations, graphical summaries and formal statistical estimates and tests. Must be able to assess quality of analysis data, perform cross study analyses and use SAS macros to automate all of the above functions. Develop analysis datasets and assist in the preparation of NDAs. A Bachelor's or Masters degree in Statistics or Computer Sciences supported by at least 4 years of industry experience is required. Good oral and written communication abilities and analytical skills are essential. Candidate will be responsible for the testing and validation of data. Candidate will interact with CRO. Technical Skills: A thorough knowledge in SAS/Base, SAS/MACRO, SAS/GRAPH, SAS/STAT and the ability to write maintainable, supportable, and well-documented SAS code is essential. Candidate needs to understand clinical data...a systems programmer will not work. Contract and Perm opportunities. Salaries are competitive with benefits.