Sr. Principal Analyst, Statistical Programming

Bilbao HR

Research Triangle Park, NC, United States
$134,000.00-$179,000.00 base; bonus/equity: cash b...
Hybrid
Sas base programming
Sas stat, graph and macro
Cdisc and/or submissions experience
The Senior Principal Analyst, Statistical Programming leads and oversees statistical programming activities, ensuring high quality, submission-ready outputs and partnering with Biostatistics

Job Summary

  • The Senior Principal Analyst, Statistical Programming leads and oversees statistical programming activities, ensuring high quality, submission-ready outputs and partnering with Biostatistics.
  • This role involves leading a drug program team of statistical programmers, managing vendor oversight, and representing Statistical Programming on study teams.
  • Biogen offers a competitive compensation package including base salary, short-term and long-term incentives, and a comprehensive benefits package supporting employee well-being.

Matching Summary

The Senior Principal Analyst, Statistical Programming leads and oversees statistical programming activities, ensuring high quality, submission-ready outputs and partnering with Biostatistics.

Salary

$134,000.00-$179,000.00 Base; Bonus/Equity: Cash bonus and equity incentive opportunities; Benefits: Medical, Dental, Vision, Life insurances, Fitness & Wellness programs, Disability insurance, Paid time off, Holidays, 401(k) match, ESPP, Tuition reimbursement

Skills & Requirements

Must-have

  • SAS Base programming
  • SAS STAT, GRAPH and MACRO
  • CDISC and/or submissions experience
  • Clinical trial experience
  • Drug development process knowledge
  • ICH and FDA/EMEA/ROW guidelines

Nice-to-have

  • Pioneering spirit
  • Think broadly
  • Drive results
  • Ethical and inclusive
  • Familiarity with AI and ML concepts

Key Requirements

  • Bachelor's degree required
  • 10 years relevant work experience
  • 10+ years SAS Base programming
  • 7+ years SAS STAT, GRAPH and MACRO
  • 10+ years relevant industry experience
  • 10+ years clinical trial experience
  • 5+ years clinical database experience
  • CDISC and/or submissions experience
  • Extensive knowledge of drug development process
  • Extensive knowledge of drug submission requirements
  • Familiarity with UNIX
  • Familiarity with software development packages (R, Imaging and Genomics)
  • Familiarity AI and ML concepts

Work Rights

Not specified

Tailored Resume

Cover Letter