Senior Statistical Programmer

ICON Clinical Research, LP

Multiple Locations
Sas programming in clinical data
Statistical analysis of clinical data
Quality control of statistical outputs
As a Senior / Principal 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 Senior / Principal 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 Senior / Principal 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 in clinical data
  • Statistical analysis of clinical data
  • Quality control of statistical outputs
  • Regulatory standards compliance

Nice-to-have

  • Collaboration with biostatisticians
  • Process improvement identification
  • Innovation and excellence fostering

Key Requirements

  • Bachelor’s or Master’s degree
  • Proficiency in SAS programming
  • Knowledge of pharmaceutical clinical development
  • Excellent analytical and problem-solving skills

Work Rights

Not specified

Tailored Resume

Cover Letter