Sr. Analyst, Statistical Programming

Bilbao HR (Biogen?)

Research Triangle Park, NC, United States
Base: $95,000.00-$124,000.00; bonus/equity: short ...
Sas base programming
Sas stat, graph, macro
Cdisc adam specifications
The Senior Analyst, Statistical Programming leads and oversees statistical programming activities both internally and externally through vendors in the application of data standards, production of analysis datasets, analysis dataset specifications, tables, listings, figures, electronic submission components, and ad hoc analyses

Job Summary

  • The Senior Analyst, Statistical Programming leads and oversees statistical programming activities both internally and externally through vendors in the application of data standards, production of analysis datasets, analysis dataset specifications, tables, listings, figures, electronic submission components, and ad hoc analyses.
  • Biogen offers a full and highly competitive range of benefits designed to support our employees’ and their families physical, financial, emotional, and social well-being.
  • We are a global team with a commitment to excellence, and a pioneering spirit, fostering an environment where individual contributions make a significant impact.

Matching Summary

The Senior Analyst, Statistical Programming leads and oversees statistical programming activities both internally and externally through vendors in the application of data standards, production of analysis datasets, analysis dataset specifications, tables, listings, figures, electronic submission components, and ad hoc analyses.

Salary

Base: $95,000.00-$124,000.00; Bonus/Equity: Short term and long-term incentives, cash bonus and equity incentive opportunities; Benefits: Medical, Dental, Vision, Life insurances, Fitness & Wellness programs, Disability insurance, Paid time off, Holidays, 401(k) with match, ESPP, Tuition reimbursement

Skills & Requirements

Must-have

  • SAS Base programming
  • SAS STAT, GRAPH, MACRO
  • CDISC ADaM specifications
  • Clinical trial experience
  • Drug development process knowledge

Nice-to-have

  • Attention to detail
  • Manage competing priorities
  • AI and ML concepts familiarity
  • Tools and process improvement collaboration

Key Requirements

  • Bachelor’s degree required
  • 5+ years relevant work experience
  • 5+ years SAS programming
  • 5+ years clinical trial experience
  • 3+ years clinical database experience
  • CDISC and/or submissions experience
  • ICH and FDA/EMEA/ROW guidelines knowledge

Work Rights

Not specified

Tailored Resume

Cover Letter