Sr Principal Analyst, Statistical Programming

Biogen Inc

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, and macro usage
Cdisc adam analysis dataset specifications
Biogen Inc is seeking a Senior Principal Analyst in Statistical Programming to lead and oversee statistical programming activities, ensuring high-quality, submission-ready outputs. The role requires extensive experience in statistical programming, clinical trials, and familiarity with CDISC standards

Job Summary

  • The role leads statistical programming activities for internal teams and external vendors to deliver high-quality, submission-ready outputs.
  • Candidates must possess extensive knowledge of CDISC standards, ICH guidelines, and FDA/EMEA submission requirements.
  • The position offers a competitive compensation package including short-term and long-term incentives along with comprehensive health and wellness benefits.

Matching Summary

Match Score: 85

Biogen Inc is seeking a Senior Principal Analyst in Statistical Programming to lead and oversee statistical programming activities, ensuring high-quality, submission-ready outputs. The role requires extensive experience in statistical programming, clinical trials, and familiarity with CDISC standards.

Salary

Base: $141,000.00-$188,000.00; Bonus/Equity: Short term and long-term incentives including cash bonus and equity; 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, and MACRO usage
  • CDISC ADaM analysis dataset specifications
  • Electronic submission components define.xml and XPTs
  • Clinical trial and drug development process knowledge

Nice-to-have

  • Familiarity with AI and ML concepts
  • Experience with R, Imaging, and Genomics software
  • UNIX environment familiarity
  • Process improvement and tool development skills
  • Strong attention to detail and ethical culture alignment

Key Requirements

  • Bachelor's degree required; Masters or PhD preferred
  • 10+ years relevant industry and clinical trial experience
  • 5+ years clinical database experience
  • Senior Principal Analyst level expertise in statistical programming

Work Rights

Not specified

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