Statistician

JOB RESPONSIBILITIES: * Support/participate in the development of clinical program * Review protocols and CRFs for soundness of trial design * Programming for developing statistical analysis outputs and validate TFLs * Perform inferential analyses; inputs to the statistical section of the clinical study report and review the publication manuscript and slides for all therapeutic area * Support/participate in project related activities including oversee CR0 deliverables for studies contracted out * Act as liaison to study team, ensuring that the clinical study is conducted in a manner that supports planned statistical analysis. With some supervision and guidance from senior departmental staff, design clinical study and help produce protocol or amendments. Perform relevant sample size calculations * Provide statistical insight into interpretation and discussion of study results * Produce / coordinate production of statistical summaries, analyses, annual reports, and related materials for submission to regulatory authorities or independent monitoring committees JOB REQUIREMENTS: Education * Ph.D. or MS degree in statistics or biostatistics field Experience * At least 5 years of biopharmaceutical experience are required

To find out more about Real please visit www.realstaffing.com [1]

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[1] http://www.realstaffing.com