Senior Programmer -  Starszy Programista

Bristol Myers Squibb

Warsaw, Poland
Base: zł209,290 - zł253,607; bonus/equity: + incen...
50% onsite
Sas programming proficiency for clinical trials
Experience with cdisc standards sdtm and adam
4+ years industry programming experience
This role provides comprehensive programming expertise to support the development and regulatory approval of Bristol Myers Squibb products

Job Summary

  • This role provides comprehensive programming expertise to support the development and regulatory approval of Bristol Myers Squibb products.
  • The position involves creating SAS programs to generate derived analysis datasets and ensuring quality through rigorous validation processes.
  • Employees benefit from a culture that values balance, flexibility, and opportunities to work on life-changing scientific breakthroughs.

Matching Summary

This role provides comprehensive programming expertise to support the development and regulatory approval of Bristol Myers Squibb products.

Salary

Base: zł209,290 - zł253,607; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Wide variety of competitive benefits and services provided

Skills & Requirements

Must-have

  • SAS programming proficiency for clinical trials
  • Experience with CDISC standards SDTM and ADaM
  • 4+ years industry programming experience
  • Knowledge of electronic submission preparation
  • Understanding of clinical data structures

Nice-to-have

  • R programming language experience
  • Linux operating system familiarity
  • Supporting regulatory filings like NDA or BLA
  • Collaborative cross-functional team skills

Key Requirements

  • Bachelor's degree in statistics, biostatistics, mathematics, computer science, or life sciences
  • Minimum 4 years of programming experience in the pharmaceutical industry
  • Proficiency in handling upstream data workflows including eDC and multiple data forms

Work Rights

Not specified

Tailored Resume

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