Collaborate with other statistical colleagues and study personnel to provide input to statistical analysis plans; Assist in and/or be accountable for selecting statistical methods for data analysis, authoring the corresponding sections of the data analysis plan, creating the reporting database, and conducting the actual analysis once a reporting database is created; Collaborate with data sciences in the planning and implementation of data quality assurance plans; Effectively justify methods selected and implement previously outlined analysis plans
Requirements:
M.S., Ph.D., or equivalent experience; Statistics, Biostatistics, Computer Science; 5+ years of relevant experience that includes 3 major pharma; Experience in all major phases of drug development that includes immunology
Text:
Clinical SAS Programmer Collaborate with other statistical colleagues and study personnel to provide input to statistical analysis plans; Assist in and/or be accountable for selecting statistical methods for data analysis, authoring the corresponding sections of the data analysis plan, creating the reporting database, and conducting the actual analysis once a reporting database is created; Collaborate with data sciences in the planning and implementation of data quality assurance plans; Effectively justify methods selected and implement previously outlined analysis plans M.S., Ph.D., or equivalent experience; Statistics, Biostatistics, Computer Science; 5+ years of relevant experience that includes 3 major pharma; Experience in all major phases of drug development that includes immunology
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