Statistician

MAIN RESPONSIBILITIES * Provide statistical support to phase I-IV clinical studies, including study design, study endpoint, statistical methodology, statistical analysis plan (SAP), mock table templates, and clinical study report * Provide programming specifications and work with SAS programmers on definitions for derived variables and data definition tables, review the efficacy and safety tables, figures and listings generated by programmer and perform independent analyses to validate key results * Provide statistical input to clinical team and perform statistical analyses for publications and to answer clinical questions * Provide statistical support to regulatory filings include summary of clinical efficacy and safety * Communicate effectively with all functional disciplines, in particular data management, medical science, clinical project management, medical marketing, regulatory affairs and marketing with a solutions-oriented approach CANDIDATE'S PROFILE * At least 4 years of pharmaceutical experience with a PhD or equivalent degree or a MS degree with more than 8 years of experience * Solid knowledge on statistical methodologies including hypothesis testing, generalized linear model, mixed effect model, longitudinal data analysis, survival analysis, and missing imputation * Working knowledge of Base SAS, SAS/STAT, SAS Macro language, and SAS/GRAPH to perform statistical analyses. Knowledge of other statistical software packages such as S-Plus or SPSS is a plus * Good oral and written communication skills * Prior experience on early phase of clinical development and knowledge of Cardiac therapeutic area is a plus * Ability to work in a fast-paced, highly entrepreneurial work environment. * Experience in oncology or inflamation are a plus

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

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