Senior Statistical Programmer I

ICON

Tokyo, Japan
Hybrid
Sas programming proficiency
Clinical trial data analysis
Statistical program development
As a Senior Statistical Programmer I 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 Senior Statistical Programmer I 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 Senior Statistical Programmer I 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 proficiency
  • Clinical trial data analysis
  • Statistical program development
  • Quality control of outputs
  • Regulatory standards compliance

Nice-to-have

  • Process improvement identification
  • Collaborative team environment
  • Effective complex information conveyance

Key Requirements

  • Bachelor's or Master's degree
  • Statistical programming experience
  • Strong SAS programming skills
  • Analytical and problem-solving skills

Work Rights

Not specified

Tailored Resume

Cover Letter