Provide statistical input for protocol development, study design, and CRF development by actively contributing to study design considerations in internal and client meetings, and providing and discussing sample size scenarios.Perform sample size calculations and write statistical methodology sections for inclusion in study protocols.Oversee production and quality control of randomization schedules, statistical analysis plans, statistical reports, statistical sections of integrated clinical reports and other process supporting documents.Design statistical analysis plans and table shells in accordance with study protocols or for integrated efficacy and safety summaries for New Drug Application (NDA) submissions.
https://www.indeed.com/viewjob?t=biostatistician&jk=7c8a9cb29b28bbe6&_ga=2.24362617.251166156.1544469794-2077807285.1533320279
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