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

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Base: $142,400.00 - $224,100.00; bonus/equity: eli...
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9 years sas programming experience in clinical trial environment
Expertise in cdisc and adam standards
Experience leading large complex statistical programming projects
** This job posting seeks an Associate Principal Scientist in Statistical Programming with a focus on late-stage clinical development for infectious diseases. The ideal candidate will have extensive experience in SAS programming within a clinical trial environment, along with strong project management and communication skills. **

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 annual bonus, long-term incentive, and a comprehensive package of benefits including medical, dental, vision, and 401(k).

Matching Summary

Match Score: 75

** This job posting seeks an Associate Principal Scientist in Statistical Programming with a focus on late-stage clinical development for infectious diseases. The ideal candidate will have extensive experience in SAS programming within a clinical trial environment, along with strong project management and communication skills. **

Salary

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

Skills & Requirements

Must-have

  • 9 years SAS programming experience in clinical trial environment
  • Expertise in CDISC and ADaM standards
  • Experience leading large complex statistical programming projects

Nice-to-have

  • Strong project management skills using Microsoft Project
  • Ability to work across cultures and geographies
  • Experience providing technical mentoring to colleagues

Key Requirements

  • BA/BS plus 9 years SAS experience or MS plus 7 years
  • US and/or worldwide drug or vaccine regulatory application submission experience
  • VISA Sponsorship available

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter