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工作職責(zé):Role Summary:Design, analyze, and interpret clinical trialsProvide statistical expertise and contributions for projects and protocols in support of clinical development.Provide statistical expertise on regulatory submissions and ensure quality and appropriateness of submission deliverables. Provide statistical expertise in maximizing the value of aggregate clinical data in support of scientific and drug development strategies.Provide study level statistical leadership and communicate resource needs to management and other line functions for the execution of statistical tasks.Responsibility:Through effective partnership with lead project statistician, provide statistical input to study designs, statistical analysis plans, interpretation of statistical results, project development plans, regulatory issues and scientific and commercialization projectsProvide planning, delivery and communication of statistical analyses, data presentations, and scientific reports, including clinical trial results, exploratory and meta-analysis results, support for publication activities, scientific presentations, and support to product defense.Accountable for study level and submission level statistical deliverables on assigned projects.Develop effective collaborations with others within Clinical R