Sr Principal Analyst, Statistical Programming

Bilbao HR (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, and macro usage
Cdisc adam analysis dataset specifications
Biogen is seeking a Senior Principal Analyst in Statistical Programming for their Cambridge, MA location, responsible for overseeing statistical programming activities and collaborating with biostatistics teams to ensure high-quality outputs. The ideal candidate will have extensive experience in statistical programming, clinical trials, and CDISC standards, along with strong leadership and communication skills

Job Summary

  • This role leads statistical programming activities for internally and externally managed vendors to ensure high-quality, submission-ready outputs.
  • The position requires extensive expertise in CDISC standards, electronic submission components like define.xml, and managing end-to-end programming deliverables.
  • Biogen offers a competitive benefits package including up to $10,000 in tuition reimbursement, equity incentives, and comprehensive health insurance.

Matching Summary

Match Score: 85

Biogen is seeking a Senior Principal Analyst in Statistical Programming for their Cambridge, MA location, responsible for overseeing statistical programming activities and collaborating with biostatistics teams to ensure high-quality outputs. The ideal candidate will have extensive experience in statistical programming, clinical trials, and CDISC standards, along with strong leadership and communication skills.

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, 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 operating system familiarity
  • Process improvement and tool development skills
  • Strong 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 ICH, FDA, and EMEA guidelines

Work Rights

Not specified

Tailored Resume

Cover Letter