Statistical Programmer Ii

ICON Clinical Research, LP

Multiple Locations
Sas programming
R programming
Clinical data analysis
Develop and validate SAS and R programs supporting the analysis and reporting of clinical and real‑world data for medical device studies

Job Summary

  • Develop and validate SAS and R programs supporting the analysis and reporting of clinical and real‑world data for medical device studies.
  • Conduct rigorous quality control checks to ensure accuracy, traceability, and consistency across all statistical outputs and deliverables.
  • Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Matching Summary

Develop and validate SAS and R programs supporting the analysis and reporting of clinical and real‑world data for medical device studies.

Skills & Requirements

Must-have

  • SAS programming
  • R programming
  • clinical data analysis
  • quality control checks
  • regulatory submissions

Nice-to-have

  • collaboration
  • problem-solving
  • data integrity
  • continuous improvement
  • scientific environment

Key Requirements

  • Bachelor's or Master's degree
  • Demonstrated experience in statistical programming
  • Proficiency in SAS programming
  • Understanding of statistical concepts
  • Clear and confident communication skills

Work Rights

Not specified

Tailored Resume

Cover Letter