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

Merck & Co., Inc.

Unknown, Unknown, United States
Base: $117,000.00 - $184,200.00; bonus/equity: ann...
Hybrid
5+ years sas programming in clinical trials
Cdisc and adam standards expertise
Development of safety and efficacy datasets
This role supports statistical programming activities for late-stage drug and vaccine clinical development projects within the BARDS department

Job Summary

  • This role 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, maintaining statistical datasets, and serving as the key point of contact through the product lifecycle.
  • Candidates will benefit from a comprehensive package including medical, dental, vision, 401(k) retirement benefits, and eligibility for annual bonuses and long-term incentives.

Matching Summary

This role 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 in clinical trials
  • CDISC and ADaM standards expertise
  • Development of safety and efficacy datasets
  • Project leadership and resource forecasting
  • Experience with global outsource team coordination

Nice-to-have

  • R programming for statistical modeling
  • Experience with US regulatory submissions
  • Mentoring junior programmers
  • Process improvement initiatives
  • Cross-cultural collaboration skills

Key Requirements

  • BA/BS plus 5 years SAS experience OR MS plus 3 years
  • US or Puerto Rico residency required
  • VISA sponsorship available

Work Rights

US and Puerto Rico Residents Only

Sponsorship: available

Tailored Resume

Cover Letter