Sr. Biostatistician

Description

Apply statistical theory and methods to the design and analysis of clinical trials.

Prepare data analysis plans and write reports describing results of statistical analysis.

Maintain expertise in state-of-the-art biometric modeling and statistical analysis techniques.

Program results in the form of text, tables, tabulations, and graphs.

Represent the Biostatistics Group in project team meetings.

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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