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Position: Principal Biostatistician
Institution: ICON plc
Location: Canada, United States
Duties: Providing statistical oversight across clinical trials in all phases and in a wide variety of therapeutic areas; Designing, planning and executing Biostatistical components of clinical trials including study design, cross functional risk assessment, writing Statistical Analysis Plans (SAP), inferential analysis programming, study reporting/submission; Functional lead responsibility for the statistics and programming portion of the study including accountability for timelines, budget and resourcing of the study; Mentoring junior Biostatisticians through our structured graduate training programme
Requirements: Master's degree in statistics or biostatistics required; Minimum of 8-10 years of biostatistical experience desired; Exhibits expertise in multiple statistical areas, the drug development process, SAS procedures, and good programming practices; Demonstrates ability to plan, supervise, implement, and monitor the statistical processes for multiple clinical trials; Displays excellent communication skills with demonstrated leadership ability; Role can be remote based anywhere in the US or Canada
   
Text: Principal Biostatistician Providing statistical oversight across clinical trials in all phases and in a wide variety of therapeutic areas; Designing, planning and executing Biostatistical components of clinical trials including study design, cross functional risk assessment, writing Statistical Analysis Plans (SAP), inferential analysis programming, study reporting/submission; Functional lead responsibility for the statistics and programming portion of the study including accountability for timelines, budget and resourcing of the study; Mentoring junior Biostatisticians through our structured graduate training programme Master's degree in statistics or biostatistics required; Minimum of 8-10 years of biostatistical experience desired; Exhibits expertise in multiple statistical areas, the drug development process, SAS procedures, and good programming practices; Demonstrates ability to plan, supervise, implement, and monitor the statistical processes for multiple clinical trials; Displays excellent communication skills with demonstrated leadership ability; Role can be remote based anywhere in the US or Canada
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