Positions range from junior to senior levels. Responsible for statistical aspects of pre-clinical through Phase IV clinical trials, including experimental design, protocol development, statistical analyses, writing statistical contributions to clinical reports and collaborating with clinical investigators, physicians and medical writers. Serve as a consulting statistician for various teams, play a key role in preparing research reports and NDA submissions for various drugs. Many therapeutic areas, including CNS, GI, Oncology, Cardio, Respiratory and HIV/AIDS.

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