Sr Principal Analyst, Statistical Programming

Biogen

Cambridge, MA, US
Base: $141,000.00-$188,000.00; bonus/equity: short...
Hybrid
10+ years sas base programming experience
7+ years sas stat graph macro usage
Cdisc adam analysis dataset specifications
Biogen is seeking a Senior Principal Analyst in Statistical Programming to lead statistical programming activities both internally and externally, ensuring the delivery of high-quality statistical outputs in compliance with industry standards. The ideal candidate should possess extensive experience in statistical programming, with a strong background in clinical trials and drug development processes

Job Summary

  • This role leads and oversees statistical programming activities for drug programs, ensuring high-quality submission-ready outputs.
  • The position requires extensive knowledge of CDISC standards, ICH guidelines, and FDA/EMEA submission requirements to manage electronic submissions.
  • Biogen offers a competitive benefits package including up to $10,000 tuition reimbursement, equity incentives, and comprehensive health coverage.

Matching Summary

Match Score: 85

Biogen is seeking a Senior Principal Analyst in Statistical Programming to lead statistical programming activities both internally and externally, ensuring the delivery of high-quality statistical outputs in compliance with industry standards. The ideal candidate should possess extensive experience in statistical programming, with a strong background in clinical trials and drug development processes.

Salary

Base: $141,000.00-$188,000.00; Bonus/Equity: Short-term cash bonus and long-term equity incentives available; Benefits: Medical, Dental, Vision, Life, 401(k) match, Tuition reimbursement up to $10,000

Skills & Requirements

Must-have

  • 10+ years SAS Base programming experience
  • 7+ years SAS STAT GRAPH MACRO usage
  • CDISC ADaM analysis dataset specifications
  • Electronic submission components define.xml XPTs
  • Clinical trial data management experience

Nice-to-have

  • Familiarity with AI and ML concepts
  • Experience with R imaging and Genomics software
  • Process improvement and training leadership
  • Strong attention to detail and ethics
  • Collaboration across cross-functional teams

Key Requirements

  • Bachelor's degree required; Masters or PhD preferred
  • 10+ years relevant industry and clinical trial experience
  • 5+ years clinical database experience
  • Extensive knowledge of drug development process
  • Not specified

Work Rights

Not specified

Tailored Resume

Cover Letter