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Position: Senior Biostatistician
Institution: ClinChoice
Location: Toronto, Ontario, Canada
Duties: Responsible for protocol development including study design, sample size estimation, randomization, and statistical analysis plan for assigned studies; Provide statistical oversight to studies and assure adequate quality and consistency with project requirements; Responsible for accuracy and completeness of database quality checks; Responsible for assuring that data for statistical analyses are complete, accurate and consistent; Responsible for statistical analysis plans and the accuracy and timeliness of statistical input into reports or decisions; Responsible for validity of analysis and alternative analysis strategies when unforeseen circumstances arise
Requirements: MS or PhD in Statistics, Biostatistics or related field. Ph.D. with 2+ years of experience or MS with 4+ years of experience; High degree of technical competence and communication skill, both oral and written; Competent in experimental design, descriptive and inferential statistics; Pharmaceutical, CRO, or related industry experience with clinical trials
   
Text: Senior Biostatistician Responsible for protocol development including study design, sample size estimation, randomization, and statistical analysis plan for assigned studies; Provide statistical oversight to studies and assure adequate quality and consistency with project requirements; Responsible for accuracy and completeness of database quality checks; Responsible for assuring that data for statistical analyses are complete, accurate and consistent; Responsible for statistical analysis plans and the accuracy and timeliness of statistical input into reports or decisions; Responsible for validity of analysis and alternative analysis strategies when unforeseen circumstances arise MS or PhD in Statistics, Biostatistics or related field. Ph.D. with 2+ years of experience or MS with 4+ years of experience; High degree of technical competence and communication skill, both oral and written; Competent in experimental design, descriptive and inferential statistics; Pharmaceutical, CRO, or related industry experience with clinical trials
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