Non-profit + 1 more
Description
Education:
Masters’ degree (or international equivalent) in statistics, biostatistics, bioinformatics or similar curriculum.
Experience:
Typically requires 5-8 years’ relevant work experience in statistical analysis of research studies
Demonstrated growth in the application of basic skills (e.g. planning and conducting analysis)
Demonstrated skills in multiple statistical areas.
Excellent interpersonal communication skills, verbal and written English.
Experience in statistical aspects of study design.
Typical Physical Demands:
Typical office environment.
Ability to spend long hours looking at computer screen and doing repetitive work on a keyboard.
Ability to sit and stand for extended periods of time. ● Ability to lift/move up to 5 lbs.
Responsibilities
Using specification documents, write statistical analysis programs using SAS or other statistical software to generate or validate analysis data sets and tables, figures, listings (TFL) for statistical reports.
As validator, investigates source of discrepancies in data and/or program code; reviews completed TFL for accuracy, including textual material (titles, headings, footnotes, etc.).
Write and maintain accurate program documentation, and generate TFL shells from existing macro or other sources.
Develop analysis data set and TFL specifications by modifying existing specs from similar studies or developing from data collection forms.
Write analysis programs in SAS or other software.
Design and generate TFL shells and analysis data set specifications, using protocol, statistical analysis plan, or other study materials.
Carry out intermediate level statistical analysis, and assess validity of analysis assumptions.
Help draft statistical sections of study reports.
Review study reports and manuscripts for accuracy of reporting and inference.
Work independently on unblinded interim analyses.
As lead statistician, manage the accurate and timely delivery of statistical services.
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