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

Merck & Co., Inc.

Rahway, NJ, USA
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 and/or large/complex late-stage drug/vaccine clinical development projects

Job Summary

  • This position supports statistical programming activities for multiple and/or large/complex late-stage drug/vaccine clinical development projects.
  • The incumbent is responsible for the design and maintenance of statistical databases that support multiple stakeholder groups including clinical development and safety evaluation.
  • The successful candidate will be eligible for an annual bonus, long-term incentive, and a comprehensive package of benefits including medical, dental, vision, and retirement plans.

Matching Summary

This position supports statistical programming activities for multiple and/or large/complex late-stage drug/vaccine clinical development projects.

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
  • Electronic submission deliverable development

Nice-to-have

  • Experience with Microsoft Project
  • Mentoring and team leadership skills
  • Process improvement initiatives
  • Global outsource partner management
  • Active professional society membership

Key Requirements

  • BA/BS plus 9 years SAS experience OR MS plus 7 years
  • US or Puerto Rico residency required
  • VISA sponsorship available

Work Rights

US and Puerto Rico Residents Only

Sponsorship: available

Tailored Resume

Cover Letter