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

Mericalherbs

Base: $142,400.00 - $224,100.00; bonus/equity: ann...
Hybrid
9 years sas programming experience in clinical trials
Expertise in cdisc and adam standards
Experience leading large complex statistical programming projects
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, outcomes research and safety evaluation.
  • The successful candidate will be eligible for annual bonus and long-term incentive, if applicable, along with 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 available; Benefits: Medical, dental, vision, 401(k), paid holidays, vacation

Skills & Requirements

Must-have

  • 9 years SAS programming experience in clinical trials
  • Expertise in CDISC and ADaM standards
  • Experience leading large complex statistical programming projects
  • Development of electronic submission deliverables
  • Knowledge of global and therapeutic area standards

Nice-to-have

  • Strong project management skills using Microsoft Project
  • Ability to work across cultures and geographies
  • Experience mentoring colleagues and outsource staff
  • Active participation in professional societies
  • Process improvement experience

Key Requirements

  • BA/BS plus 9 years SAS experience OR MS plus 7 years SAS experience
  • US and/or worldwide drug or vaccine regulatory application submission experience
  • Eligible for US employment (Visa Sponsorship: Yes)

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter