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

539

Unknown, Unknown, United States
Base: $142,400.00 - $224,100.00; bonus/equity: ann...
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9+ years sas programming experience in clinical trials
Cdisc and adam standards expertise
Leadership of global statistical programming teams
** This job posting seeks an Associate Principal Scientist in Statistical Programming within the Biostatistics and Research Decision Sciences (BARDS) department of a prominent pharmaceutical company. The role involves supporting late-stage drug and vaccine development through statistical programming, requiring extensive SAS experience and project management skills. **

Job Summary

  • This role supports statistical programming activities for multiple late-stage drug and vaccine clinical development projects within the BARDS department.
  • The incumbent serves as the statistical programming point of contact and knowledge holder through the entire product lifecycle, ensuring timely and high-quality deliverables.
  • 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

Match Score: 75

** This job posting seeks an Associate Principal Scientist in Statistical Programming within the Biostatistics and Research Decision Sciences (BARDS) department of a prominent pharmaceutical company. The role involves supporting late-stage drug and vaccine development through statistical programming, requiring extensive SAS experience and project management skills. **

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 in clinical trials
  • CDISC and ADaM standards expertise
  • Leadership of global statistical programming teams
  • Development of regulatory submission deliverables
  • Experience with US or worldwide drug/vaccine submissions

Nice-to-have

  • Proficiency in R or Python programming languages
  • Experience mentoring junior colleagues
  • Active participation in professional societies
  • Process improvement initiatives experience
  • Cross-cultural collaboration skills

Key Requirements

  • BA/BS plus 9+ years SAS experience OR MS plus 7+ years SAS experience
  • US and/or worldwide regulatory application submission experience at leadership level
  • Strong project management and resource forecasting capabilities

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter