Assoc. Principal Scientist Stat. Programming - Late-stage, Infectious Disease (hybrid)

Merck & Co., Inc.

Base: $142,400.00 - $224,100.00; bonus/equity: ann...
Hybrid
9 years sas programming experience
Clinical trial environment expertise
Cdisc and adam standards knowledge
This position supports statistical programming activities for multiple large and complex late-stage drug and vaccine clinical development projects within the BARDS department

Job Summary

  • This position supports statistical programming activities for multiple large and complex late-stage drug and vaccine clinical development projects within the BARDS department.
  • The incumbent serves as the statistical programming point of contact through the entire product lifecycle, ensuring high-quality deliverables for worldwide regulatory application submissions.
  • 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 multiple large and complex late-stage drug and vaccine clinical development projects within the BARDS department.

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
  • Clinical trial environment expertise
  • CDISC and ADaM standards knowledge
  • Lead complex statistical programming projects
  • US drug regulatory submission experience

Nice-to-have

  • Mentoring global programming teams
  • Experience with Microsoft Project
  • Process improvement initiatives
  • Cross-cultural collaboration skills
  • Active professional society membership

Key Requirements

  • BA/BS plus 9 years SAS experience OR MS plus 7 years
  • Experience leading large statistical programming projects
  • Expertise in SAS/MACRO, SAS/GRAPH, and data steps
  • Leadership level regulatory submission experience
  • Strong project management and stakeholder engagement skills

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter