Statistical Programmer (all Levels)

ICON Clinical Research, LP

Taipei, Taiwan
Fully remote
Sas programming
Statistical analysis
Clinical trial data
As a Statistical Programmer at ICON, you will play a crucial role in analyzing clinical trial data and supporting the statistical analysis process to ensure high-quality results

Job Summary

  • As a Statistical Programmer at ICON, you will play a crucial role in analyzing clinical trial data and supporting the statistical analysis process to ensure high-quality results.
  • You will contribute to the success of our clinical studies by developing and validating statistical programs, collaborating with biostatisticians, and ensuring compliance with regulatory standards.
  • ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work-life balance opportunities for you and your family.

Matching Summary

As a Statistical Programmer at ICON, you will play a crucial role in analyzing clinical trial data and supporting the statistical analysis process to ensure high-quality results.

Skills & Requirements

Must-have

  • SAS programming
  • Statistical analysis
  • Clinical trial data
  • Regulatory standards compliance
  • Quality control checks

Nice-to-have

  • Process improvement identification
  • Team collaboration
  • Innovation and excellence
  • Work-life balance focus

Key Requirements

  • Bachelor’s or Master’s degree
  • Experience in statistical programming
  • Proficiency in SAS programming
  • Understanding of statistical concepts
  • Analytical and problem-solving skills

Work Rights

Not specified

Tailored Resume

Cover Letter