Study Lead Programmer

ICON Clinical Research, LP

Multiple Locations
Sas programming
Statistical program development
Data manipulation and analysis
Support the development and validation of statistical programs that drive high-quality clinical trial analysis and reporting

Job Summary

  • Support the development and validation of statistical programs that drive high-quality clinical trial analysis and reporting.
  • Work closely with senior statistical programmers and biostatisticians to interpret project requirements and contribute to Statistical Analysis Plans.
  • ICON offers a range of benefits designed to be competitive and focused on well-being and work-life balance.

Matching Summary

Support the development and validation of statistical programs that drive high-quality clinical trial analysis and reporting.

Skills & Requirements

Must-have

  • SAS programming
  • statistical program development
  • data manipulation and analysis
  • clinical trial reporting
  • CDISC standards
  • ADaM dataset development

Nice-to-have

  • proactive attitude
  • problem-solving skills
  • collaborative team player
  • fast-paced environment
  • clinical trials knowledge

Key Requirements

  • Bachelor's degree in Statistics, Mathematics, Computer Science, or related field
  • Foundational knowledge of SAS in a clinical trials setting
  • Familiarity with SDTM and ADaM datasets

Work Rights

Not specified

Tailored Resume

Cover Letter