Senior Principal Statistical Programmer

Novartis UK

East Hanover, New Jersey, US
$119,700 - $222,300 py; performance-based cash inc...
Fully remote
Sas/r programming expertise
Cdisc data standards
Clinical trial programming
Lead statistical programming activities for clinical trials or programs, including coordination of internal/external programmers and making strategic programming decisions

Job Summary

  • Lead statistical programming activities for clinical trials or programs, including coordination of internal/external programmers and making strategic programming decisions.
  • Ensure timely and quality development and validation of datasets and outputs for clinical study reports, regulatory submissions, and other required analyses.
  • Maintain advanced knowledge of programming software (SAS, R) and industry requirements (CDISC, eCTD, Define.xml) while acting as a programming expert in problem-solving.

Matching Summary

Lead statistical programming activities for clinical trials or programs, including coordination of internal/external programmers and making strategic programming decisions.

Salary

$119,700 - $222,300 per year; Performance-based cash incentive and potential equity awards; Comprehensive benefits package including health, 401(k), and generous time off

Skills & Requirements

Must-have

  • SAS/R programming expertise
  • CDISC data standards
  • Clinical trial programming
  • Statistical analysis plans
  • Regulatory submissions

Nice-to-have

  • Cross-functional team collaboration
  • Process improvement initiatives
  • Knowledge sharing
  • Problem-solving expert

Key Requirements

  • 7+ years programming experience
  • BS degree in relevant field
  • Trial/Lead/Program Programmer experience
  • Advanced SAS/R macro development
  • Experience with programming specifications

Work Rights

Not specified

Tailored Resume

Cover Letter