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

Laboratory Animal Management Association

Multiple Locations
Base: $142,400.00 - $224,100.00; bonus/equity: eli...
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Sas programming in clinical trials
Develop analysis and reporting deliverables
Coordinate global programming teams
** The Laboratory Animal Management Association is seeking an Associate Principal Scientist in Statistical Programming, focusing on late-stage drug and vaccine development. The role requires extensive experience in SAS programming within clinical trials and emphasizes collaboration, project management, and the execution of statistical analysis deliverables. **

Job Summary

  • This position supports statistical programming activities for multiple late-stage drug/vaccine clinical development projects, encompassing the development and execution of statistical analysis and reporting deliverables.
  • The incumbent will serve as the statistical programming point of contact and knowledge holder through the entire product lifecycle, collaborating with statistics and other project stakeholders.
  • The role involves effective analysis and report programming development and validation, maintaining project plans, coordinating global programming teams, and contributing to departmental strategic initiatives.

Matching Summary

Match Score: 75

** The Laboratory Animal Management Association is seeking an Associate Principal Scientist in Statistical Programming, focusing on late-stage drug and vaccine development. The role requires extensive experience in SAS programming within clinical trials and emphasizes collaboration, project management, and the execution of statistical analysis deliverables. **

Salary

Base: $142,400.00 - $224,100.00; Bonus/Equity: eligible for annual bonus and long-term incentive; 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
  • Develop analysis and reporting deliverables
  • Coordinate global programming teams
  • Regulatory application submission experience
  • CDISC and ADaM standards expertise

Nice-to-have

  • Experience with R or Python
  • Mentoring colleagues
  • Process improvement experience
  • Work across cultures and geographies

Key Requirements

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

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter