Study Lead Programmer

ICON plc

Not specified; not specified; competitive within e...
Sas programming experience in clinical trials
R programming experience in clinical trials
Cdisc standards familiarity sdtm and adam
The role involves supporting the development and validation of statistical programs to drive high-quality clinical trial analysis and reporting

Job Summary

  • The role involves supporting the development and validation of statistical programs to drive high-quality clinical trial analysis and reporting.
  • Candidates will work closely with senior statisticians to interpret requirements and contribute to Statistical Analysis Plans while ensuring data integrity.
  • ICON offers a competitive salary, diverse benefits including health insurance and retirement planning, and a culture focused on inclusion and well-being.

Matching Summary

The role involves supporting the development and validation of statistical programs to drive high-quality clinical trial analysis and reporting.

Salary

Not specified; Not specified; Competitive within each country with various annual leave, health insurance, and retirement offerings

Skills & Requirements

Must-have

  • SAS programming experience in clinical trials
  • R programming experience in clinical trials
  • CDISC standards familiarity SDTM and ADaM
  • Bachelor's degree in Statistics or related field

Nice-to-have

  • Strong analytical mindset and attention to detail
  • Collaborative team player with communication skills
  • Proactive attitude toward learning and problem-solving

Key Requirements

  • Bachelor's degree in Statistics, Mathematics, Computer Science, or related field
  • Experience with SAS and R in a clinical trials setting

Work Rights

Not specified

Tailored Resume

Cover Letter