Sr. Analyst, Statistical Programming

Biogen

Cambridge, MA, US
Base: $100,000.00-$130,000.00; bonus/equity: short...
Hybrid
5+ years sas base programming experience
5+ years clinical trial experience
Cdisc adam specification authoring
The role involves leading a study team of statistical programmers to deliver high-quality, submission-ready outputs in partnership with Biostatistics

Job Summary

  • The role involves leading a study team of statistical programmers to deliver high-quality, submission-ready outputs in partnership with Biostatistics.
  • Candidates will be responsible for implementing data strategies and ensuring compliance with ICH, FDA, and EMEA guidelines throughout the drug development process.
  • Biogen offers a comprehensive benefits package including up to $10,000 in tuition reimbursement, paid parental leave, and equity incentive opportunities.

Matching Summary

The role involves leading a study team of statistical programmers to deliver high-quality, submission-ready outputs in partnership with Biostatistics.

Salary

Base: $100,000.00-$130,000.00; Bonus/Equity: Short-term and long-term incentives including cash bonus and equity; Benefits: Medical, Dental, Vision, Life, 401(k) match, Tuition reimbursement

Skills & Requirements

Must-have

  • 5+ years SAS Base programming experience
  • 5+ years clinical trial experience
  • CDISC ADaM specification authoring
  • Electronic submission component preparation
  • Vendor management and oversight

Nice-to-have

  • Familiarity with UNIX environment
  • Knowledge of R software packages
  • Experience with imaging and genomics tools
  • Strong attention to detail
  • Ability to manage competing priorities

Key Requirements

  • Bachelor's degree required
  • 5+ years relevant industry experience
  • 3+ years clinical database experience
  • Knowledge of drug submission requirements

Work Rights

Not specified

Tailored Resume

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