Sr. Principal Analyst, Statistical Programming

Biogen

Remote, , United States
Base: $134,000.00-$179,000.00; bonus/equity: short...
Fully remote
Statistical programming expertise
Cdisc adam dataset specification
Clinical trial data management
The Senior Principal Analyst, Statistical Programming leads a drug program team to deliver high quality, submission ready statistical outputs and manages vendor relationships

Job Summary

  • The Senior Principal Analyst, Statistical Programming leads a drug program team to deliver high quality, submission ready statistical outputs and manages vendor relationships.
  • Biogen offers a comprehensive benefits package including medical, dental, vision, life insurance, fitness programs, paid time off, parental leave, 401(k) matching, and tuition reimbursement.
  • Biogen is committed to a culture of inclusion and belonging, valuing diverse backgrounds and perspectives to foster innovation and employee empowerment.

Matching Summary

The Senior Principal Analyst, Statistical Programming leads a drug program team to deliver high quality, submission ready statistical outputs and manages vendor relationships.

Salary

Base: $134,000.00-$179,000.00; Bonus/Equity: Short and long-term incentives including cash bonus and equity; Benefits: Medical, dental, vision, life insurance, fitness programs, paid time off, parental leave, 401(k) matching, tuition reimbursement

Skills & Requirements

Must-have

  • Statistical programming expertise
  • CDISC ADaM dataset specification
  • Clinical trial data management
  • SAS Base, STAT, GRAPH, MACRO programming
  • Electronic submission preparation
  • Drug development process knowledge
  • Vendor management and oversight

Nice-to-have

  • Familiarity with AI and ML concepts
  • UNIX and software development packages
  • Process improvement and training
  • Cross-functional collaboration
  • Strong attention to detail
  • Inclusive and ethical culture
  • Leadership and communication skills

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
  • Must be located in the United States

Work Rights

Must be located in the United States

Tailored Resume

Cover Letter