Assoc Prin. Scientist Statistical Programming, Late-stage (hybrid)

med-in.at

Rahway, New Jersey, USA
Base: $142,400.00 - $224,100.00; bonus/equity: ann...
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Sas programming in clinical trials
Statistical analysis and reporting
Clinical data management concepts
** This job posting is for an Associate Principal Scientist in Statistical Programming at Med-in.at, located in Rahway, New Jersey, offering a hybrid work model. The position focuses on statistical programming for late-stage drug and vaccine clinical development, requiring significant SAS programming experience and project management skills. **

Job Summary

  • This position supports statistical programming activities for multiple late-stage drug/vaccine clinical development projects.
  • The incumbent is responsible for the design and maintenance of statistical datasets that support multiple stakeholder groups.
  • The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.

Matching Summary

Match Score: 75

** This job posting is for an Associate Principal Scientist in Statistical Programming at Med-in.at, located in Rahway, New Jersey, offering a hybrid work model. The position focuses on statistical programming for late-stage drug and vaccine clinical development, requiring significant SAS programming experience and project management skills. **

Salary

Base: $142,400.00 - $224,100.00; Bonus/Equity: Annual bonus and long-term incentive, if applicable; Benefits: Medical, dental, vision healthcare and other insurance benefits, retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days.

Skills & Requirements

Must-have

  • SAS programming in clinical trials
  • Statistical analysis and reporting
  • Clinical data management concepts
  • CDISC and ADaM standards
  • Global programming team coordination

Nice-to-have

  • Cross-cultural collaboration
  • Process improvement initiatives
  • Mentoring colleagues
  • Experience with R or Python

Key Requirements

  • BA/BS + 9 years SAS programming
  • MS + 7 years SAS programming
  • Significant expertise in SAS and clinical trial programming
  • US and/or worldwide regulatory application submission experience
  • Experience leading large/complex statistical programming projects

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter