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Mid-level, metro location and moderately strong CRO brand increase applicant density.
Clinical trial statistical programming skills are specialized and less transferable across industries.
Explicit 5+ years, mandatory SAS/R clinical programming experience and ICH/GCP regulatory requirements make filtering strict.
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Develop, validate, and maintain complex statistical programs (SAS, R, etc.) for clinical trial data manipulation, analysis, and reporting.
Collaborate with biostatisticians and cross-functional teams to implement statistical analyses according to study requirements and regulatory standards.
Mentor junior programmers and contribute to training on programming techniques and best practices.
Bachelor's degree in statistics, mathematics, computer science, or related field required; advanced degree is a plus.
5+ years of experience as a statistical programmer in clinical research with strong knowledge of statistical methodologies and programming.
Proficiency in SAS and R programming languages; exposure to Python and R Shiny.
Employment contingent on legal right to work in the country of the role.
Experienced in clinical research environments with familiarity of ICH/GCP guidelines and regulatory compliance.
Operates effectively both independently and in cross-functional teams with strong communication skills to explain statistical concepts to non-technical stakeholders.
Demonstrates leadership through mentoring and training junior programmers.