ICON seeks a Statistical Analyst to support clinical trial activities, including study design input, statistical methods documentation, and SAS-based programming. The role involves collaborating across teams to deliver high-quality statistical analyses and study deliverables.
Responsibilities
Support study initiation by providing input on design, protocols, and case report forms
Write statistical methods sections including sample size and power calculations
Develop and assist with statistical analysis plans and table shells
Review database specifications and lead initial raw variable review
Program statistical procedures including repeated measures and survival analyses using SAS/Graph
Requirements
4+ years statistical programming experience in pharmaceutical, biotechnology, or CRO settings
Strong SAS programming expertise with clinical trial and statistical analysis background
Knowledge of R programming with willingness to develop proficiency
Comprehensive understanding of CDISC standards (SDTM and ADaM)
Experience developing, validating, and maintaining production-quality code
Proficiency with Pinnacle 21 for CDISC compliance and data validation
Excellent analytical, problem-solving, and cross-functional collaboration skills
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