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

Merck & Co., Inc.

Base: $117,000.00 - $184,200.00; bonus/equity: ann...
Hybrid
5 years sas programming experience
Clinical trial environment expertise
Cdisc and adam standards knowledge
This position supports statistical programming activities for late-stage drug and vaccine clinical development projects, including regulatory submissions

Job Summary

  • This position supports statistical programming activities for late-stage drug and vaccine clinical development projects, including regulatory submissions.
  • The incumbent serves as the statistical programming point of contact throughout the product lifecycle, ensuring high-quality deliverables for multiple stakeholder groups.
  • Employees are eligible for an annual bonus, long-term incentives, and a comprehensive benefits package including medical, dental, vision, and 401(k) retirement plans.

Matching Summary

This position supports statistical programming activities for late-stage drug and vaccine clinical development projects, including regulatory submissions.

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, vacation

Skills & Requirements

Must-have

  • 5 years SAS programming experience
  • Clinical trial environment expertise
  • CDISC and ADaM standards knowledge
  • Statistical dataset design and maintenance
  • Project leadership in global teams

Nice-to-have

  • Experience with Microsoft Project
  • Active in professional societies
  • Process improvement background
  • Cross-cultural collaboration ability
  • Mentoring junior programmers

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