Associate Director Statistical Programming

Novartis UK

East Hanover, New Jersey, United States
Base: $145,600 - $270,400 py; bonus/equity: perfor...
Fully remote
Sas or r programming expertise
Cdisc standards knowledge
Clinical trial methodology
This role involves leading statistical programming activities for multiple clinical trials within a program or indication area while ensuring timely and quality deliverables

Job Summary

  • This role involves leading statistical programming activities for multiple clinical trials within a program or indication area while ensuring timely and quality deliverables.
  • The position requires acting as a subject matter expert during audits and inspections, representing the company at industry working groups and health authority meetings.
  • Candidates will receive a comprehensive benefits package including health, life, disability benefits, a 401(k) with match, and eligibility for annual equity awards.

Matching Summary

This role involves leading statistical programming activities for multiple clinical trials within a program or indication area while ensuring timely and quality deliverables.

Salary

Base: $145,600 - $270,400 per year; Bonus/Equity: Performance-based cash incentive and annual equity awards eligible; Benefits: Health, life, disability, 401(k) match, vacation, personal days, holidays

Skills & Requirements

Must-have

  • SAS or R programming expertise
  • CDISC standards knowledge
  • Clinical trial methodology
  • Statistical analysis plan development
  • Audit readiness management

Nice-to-have

  • Strategic technical leadership
  • Global collaboration skills
  • Mentoring junior programmers
  • Conference representation
  • Non-clinical initiative leadership

Key Requirements

  • BS/MS degree in life science or related field
  • 6+ years in programming or statistical role
  • 3+ years line management experience
  • 2+ years as Lead/Program Programmer
  • Expert in SAS or R programming

Work Rights

Not specified

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