Sr. Principal Analyst, Statistical Programming

Biogen

Research Triangle Park, NC, United States
Base: $134,000.00-$179,000.00; bonus/equity: cash ...
Hybrid
Statistical programming leadership
Cdisc adam analysis data sets
Clinical trial data management
The Senior Principal Analyst, Statistical Programming leads statistical programming efforts to deliver high quality, submission ready outputs and manages vendor quality oversight

Job Summary

  • The Senior Principal Analyst, Statistical Programming leads statistical programming efforts to deliver high quality, submission ready outputs and manages vendor quality oversight.
  • Biogen offers a competitive compensation package including base salary, cash bonus, equity incentives, and a comprehensive benefits program supporting employees’ physical, financial, emotional, and social well-being.
  • The company fosters a culture of inclusion, pioneering spirit, and collaboration, providing opportunities for learning, growth, and impactful contributions to life-changing medicines.

Matching Summary

The Senior Principal Analyst, Statistical Programming leads statistical programming efforts to deliver high quality, submission ready outputs and manages vendor quality oversight.

Salary

Base: $134,000.00-$179,000.00; Bonus/Equity: Cash bonus and equity incentive opportunities; Benefits: Medical, dental, vision, life insurance, wellness programs, paid time off, 401(k) with match, tuition reimbursement

Skills & Requirements

Must-have

  • Statistical programming leadership
  • CDISC ADaM analysis data sets
  • Clinical trial data management
  • SAS Base, STAT, GRAPH, MACRO programming
  • Electronic submission preparation
  • Drug development process knowledge

Nice-to-have

  • Familiarity with UNIX and R software
  • AI and ML concepts knowledge
  • Process improvement and training
  • Cross-functional collaboration
  • Strong attention to detail
  • Inclusive and ethical culture fit

Key Requirements

  • Bachelor’s degree required
  • Masters or PhD in Statistics or Mathematics preferred
  • 10+ years relevant work experience
  • 10+ years SAS programming experience
  • 10+ years clinical trial experience
  • 5+ years clinical database experience
  • CDISC and submissions experience
  • Knowledge of ICH and FDA/EMEA/ROW guidelines

Work Rights

Not specified

Tailored Resume

Cover Letter