Sr. Scientist Stat Programming, Late-stage Development (hybrid)

539

Unknown, Unknown, US
Base: $117,000.00 - $184,200.00; bonus/equity: ann...
Hybrid
5+ years sas programming experience
Clinical trial programming expertise
Cdisc and adam standards knowledge
This position supports statistical programming activities for late-stage drug and vaccine clinical development projects within the BARDS department

Job Summary

  • This position supports statistical programming activities for late-stage drug and vaccine clinical development projects within the BARDS department.
  • The incumbent is responsible for designing complex programming algorithms and ensuring compliance with CDISC and ADaM standards for regulatory submissions.
  • Candidates will lead project plans, coordinate global programming teams, and serve as the key point of contact for statistical programming throughout the product lifecycle.

Matching Summary

This position supports statistical programming activities for late-stage drug and vaccine clinical development projects within the BARDS department.

Salary

Base: $117,000.00 - $184,200.00; Bonus/Equity: Annual bonus and long-term incentive eligible; Benefits: Medical, dental, vision, 401(k), paid holidays

Skills & Requirements

Must-have

  • 5+ years SAS programming experience
  • Clinical trial programming expertise
  • CDISC and ADaM standards knowledge
  • Statistical analysis deliverable development
  • Project management and resource forecasting

Nice-to-have

  • R programming for statistical modeling
  • Experience with global outsource partners
  • Strategic thinking and process improvement
  • Mentoring junior programmers
  • Active in professional societies

Key Requirements

  • BA/BS plus 5 years SAS experience OR MS plus 3 years
  • US work authorization required (VISA sponsorship available)
  • Experience with electronic submission deliverables

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter