Leader in bringing innovative statistical thinking and methods to help drive applications of suit-for-purpose statistical methods that enhance the probability of successes for clinical development programs; Collaborate with internal and external stakeholders to ensure effective quantitative approaches are applied to the collection and analysis of a wide variety of data types; Develop statistical sections of clinical development plans, protocols, statistical analysis plans, and key specifications for statistical programming implementation of analyses
Requirements:
PhD in statistics (or equivalent degree) with 6+ years or master with 9+ years of relevant working experience in Biotech, Pharma, Regulatory agencies, or Clinical Research Organizations; Excellent statistical knowledge with the ability of applying the knowledge to solve scientific and clinical problems; Working knowledge of relevant ICH guidelines, US, EU and other regions’ regulations; Experience working on oncology, vaccine/infectious disease and rare disease clinical studies and regulatory interactions are preferred
Text:
Associate Director, Biostatistics Leader in bringing innovative statistical thinking and methods to help drive applications of suit-for-purpose statistical methods that enhance the probability of successes for clinical development programs; Collaborate with internal and external stakeholders to ensure effective quantitative approaches are applied to the collection and analysis of a wide variety of data types; Develop statistical sections of clinical development plans, protocols, statistical analysis plans, and key specifications for statistical programming implementation of analyses PhD in statistics (or equivalent degree) with 6+ years or master with 9+ years of relevant working experience in Biotech, Pharma, Regulatory agencies, or Clinical Research Organizations; Excellent statistical knowledge with the ability of applying the knowledge to solve scientific and clinical problems; Working knowledge of relevant ICH guidelines, US, EU and other regions’ regulations; Experience working on oncology, vaccine/infectious disease and rare disease clinical studies and regulatory interactions are preferred
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