Senior Statistical Programmer

ICON

Multiple Locations
Sas programming expertise
Statistical programming in clinical research
Quality control of statistical outputs
At ICON, you’ll play an integral role in transforming clinical trial data into meaningful insights that drive critical decision‑making in global healthcare

Job Summary

  • At ICON, you’ll play an integral role in transforming clinical trial data into meaningful insights that drive critical decision‑making in global healthcare.
  • Your expertise will directly support the success of our clinical studies and the advancement of life‑changing therapies.
  • ICON offers a diverse culture that rewards high performance and nurtures talent, with competitive benefits focused on well-being and work-life balance.

Matching Summary

At ICON, you’ll play an integral role in transforming clinical trial data into meaningful insights that drive critical decision‑making in global healthcare.

Skills & Requirements

Must-have

  • SAS programming expertise
  • statistical programming in clinical research
  • quality control of statistical outputs
  • collaboration with biostatisticians
  • clinical trial data analysis

Nice-to-have

  • continuous improvement and innovation
  • effective communication skills
  • teamwork and collaboration
  • translating complex analyses into insights

Key Requirements

  • Bachelor’s or Master’s degree in Statistics, Mathematics, Computer Science, or related discipline
  • proven experience in statistical programming within clinical research or pharmaceutical industry
  • strong grounding in statistical concepts and clinical data analysis

Work Rights

Not specified

Tailored Resume

Cover Letter