Assoc Prin. Scientist Statistical Programming, Late-stage (hybrid)

Nerdgigs

Rahway, New Jersey, USA
$142,400.00 - $224,100.00; bonus + long-term incen...
Hybrid
Sas programming in clinical trials
Statistical analysis and reporting
Cdisc and adam standards
This position supports statistical programming activities for multiple late-stage drug/vaccine clinical development projects, ranging from individual trials to worldwide regulatory submissions

Job Summary

  • This position supports statistical programming activities for multiple late-stage drug/vaccine clinical development projects, ranging from individual trials to worldwide regulatory submissions.
  • The incumbent is responsible for the design and maintenance of statistical datasets supporting various stakeholder groups and serves as the programming point of contact throughout the product lifecycle.
  • The role involves effective analysis and report programming development and validation, maintaining project plans, and coordinating global programming teams, including outsource providers.

Matching Summary

This position supports statistical programming activities for multiple late-stage drug/vaccine clinical development projects, ranging from individual trials to worldwide regulatory submissions.

Salary

$142,400.00 - $224,100.00; Bonus and long-term incentive eligible; Comprehensive benefits package

Skills & Requirements

Must-have

  • SAS programming in clinical trials
  • Statistical analysis and reporting
  • CDISC and ADaM standards
  • Regulatory application submission experience
  • Global programming team coordination

Nice-to-have

  • Experience with R or Python
  • Knowledge of SDLC processes
  • Mentoring and guidance experience
  • Cross-cultural collaboration
  • Project plan management with MS Project

Key Requirements

  • 9+ years SAS programming experience (BA/BS)
  • 7+ years SAS programming experience (MS)
  • Significant expertise in SAS and clinical trial programming
  • Experience leading large statistical programming projects
  • US and/or worldwide drug/vaccine regulatory submission leadership

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter