Principal Statistical Programmer

ICON conducts clinical research to help bring medicines and treatments to patients. This role leads statistical programming for clinical trials and regulatory submissions, working with clinical teams and mentoring junior programmers.

• Lead development and validation of statistical programs for analysis and reporting
• Collaborate with biostatisticians and clinical teams to define study requirements
• Oversee programming specifications, documentation and regulatory technical reports
• Mentor junior statistical programmers
• Maintain production-quality code and support CDISC compliance checks

Experience

7+ years

Domain

clinical research

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