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Senior Statistical Programmer II

ICON · Bangalore, India

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BiometricsFull-timeCompany career page

The apply link worked recently (not employer-confirmed).

What they're looking for

  • 10+ years clinical programming experience with progressive trial responsibilities
  • Expert SAS programming skills and CDISC SDTM standards knowledge
  • Proven trial leadership experience managing programming teams and study deliverables
  • Demonstrated expertise in macros, edit checks, visualizations, and submission packages
  • Strong cross-functional collaboration and mentoring capabilities
  • Legal right to work in country where role is based

What you'll be doing

  • Design, develop, and validate SAS programs for statistical analysis and clinical trial reporting
  • Collaborate with biostatisticians to create analysis plans and implement statistical methods
  • Perform quality control checks and review outputs for regulatory compliance
  • Support preparation of statistical reports, presentations, and regulatory submissions
  • Mentor junior programmers and share technical best practices with team members

Privacy & handoff

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RoleLantern checkedNeeds clarity
Date posted8 days ago
Last source checkToday
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