Sr. Biostatistician

1 Apply statistical theory and methods to the design and analysis of clinical trials. 2 Prepare data analysis plans and write reports describing results of statistical analysis. 3 Maintain expertise in state-of-the-art biometric modeling and statistical analysis techniques. 4 Program results in the form of text, tables, tabulations, and graphs. 5 Represent the Biostatistics Group in project team meetings. 6 Consult with research scientists, medical directors, and clinical managers on statistical questions. A degree in biostatistics or statistics, MS or PhD with a strong theoretical background in statistics is required. The MS candidate should have at least 3 years experience in clinical trials, preferably in the pharmaceutical industry. A PhD candidate will be considered with 1year university experience. -Some knowledge in medicine and/or life sciences is essential. -Knowledge of SAS programming for statistical analysis and data manipulation is essential. -Knowledge of other statistical analysis software is desirable. -Likewise, knowledge of good clinical practice would be valuable. Key Words - Biostatistician, SAS, Statistics, Clinical Trials, Pharmaceuitcal industry

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