Associate Principal Scientist Statistical Programming - Late-stage (non-oncology) (hybrid)

Merck Sharp & Dohme Corp

United States
Base: $142,400.00 - $224,100.00; bonus/equity: ann...
Hybrid (3 days onsite, 1 day remote)
9 years sas programming experience in clinical trial environment
Experience leading large complex statistical programming projects
Expertise in sas/macro, sas/graph, and cdisc adam standards
Merck Sharp & Dohme Corp is seeking an Associate Principal Scientist in Statistical Programming for late-stage clinical development projects, with a focus on statistical analysis and reporting. The role requires extensive SAS programming experience and offers a hybrid work model with a comprehensive benefits package

Job Summary

  • This position supports statistical programming activities for multiple and/or large/complex late-stage drug/vaccine clinical development projects within the BARDS department.
  • The incumbent serves as the statistical programming point of contact and knowledge holder through the entire product lifecycle, ensuring high-quality deliverables and process compliance.
  • The successful candidate will be eligible for an annual bonus, long-term incentives, and a comprehensive benefits package including medical, dental, vision, and 401(k) retirement plans.

Matching Summary

Match Score: 85

Merck Sharp & Dohme Corp is seeking an Associate Principal Scientist in Statistical Programming for late-stage clinical development projects, with a focus on statistical analysis and reporting. The role requires extensive SAS programming experience and offers a hybrid work model with a comprehensive benefits package.

Salary

Base: $142,400.00 - $224,100.00; Bonus/Equity: Annual bonus and long-term incentive eligible; Benefits: Medical, dental, vision, 401(k), paid holidays, vacation

Skills & Requirements

Must-have

  • 9 years SAS programming experience in clinical trial environment
  • Experience leading large complex statistical programming projects
  • Expertise in SAS/MACRO, SAS/GRAPH, and CDISC ADaM standards
  • US or worldwide drug regulatory application submission experience
  • Ability to coordinate global programming teams including outsource staff

Nice-to-have

  • Strong working knowledge of reporting processes and SDLC
  • Experience with Microsoft Project for project planning
  • Active participation in professional societies
  • Interest in process improvement initiatives
  • Ability to work across cultures and geographies

Key Requirements

  • BA/BS plus 9 years SAS experience OR MS plus 7 years SAS experience
  • VISA Sponsorship available
  • Domestic relocation eligibility required

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter