Responsibilities: Provide statistical input into the design of protocols including preparation of the biostatistical analysis section. Suggest optimal statistical designs that are acceptable by regulators Prepare statistical analysis plans including table shells. Analyze and report results of clinical trials. Provide tables, listings and graphs for final study reports. Provide ad hoc / data driven analyses. Provide statistical input for the preparation of final study reports and other required documents. Provide statistical support for integrated reports, submissions preparation, and post-submission activities. Contribute to clinical development plan
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