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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