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Mid-level, metro-based clinical SAS/R role at a known CRO; niche skills reduce applicant density.
Strong clinical research and regulatory domain requirements limit cross-industry transferability.
Mandatory 5+ years plus SAS/R and clinical/regulatory experience creates stringent shortlisting filters.
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Develop, validate, and maintain complex statistical programs (SAS, R, and similar) for clinical trial data manipulation, analysis, and reporting.
Collaborate with biostatisticians and cross-functional teams to interpret study requirements and implement statistical analyses accurately.
Prepare and review statistical analysis plans, programming specifications, and derived datasets ensuring compliance with regulatory standards.
Bachelor’s degree in statistics, mathematics, computer science, or related field; advanced degree is a plus.
At least 5 years of experience as a statistical programmer in clinical research industry.
Proficiency in SAS and R programming languages; experience with Python and R Shiny is beneficial.
Employment contingent on legal right to work in the country where the role is based.
Experienced in clinical trial statistical programming with strong knowledge of statistical methodologies and regulatory compliance (ICH/GCP).
Demonstrates capability in mentoring junior programmers and sharing best practices within teams.
Skilled at communicating complex statistical concepts to non-technical stakeholders and collaborating cross-functionally.