Manager, Biostats

Bristol Myers Squibb

Warsaw, Poland
Base: zł209,290 - zł253,607; bonus/equity: + incen...
Hybrid (50% onsite)
Clinical trial design
Statistical analysis plan
Sas, r or python programming
Bristol Myers Squibb is seeking a Manager of Biostatistics in Warsaw, Poland, to contribute to clinical trial design, analysis, and regulatory submissions. The role requires a fresh MS in statistics or biostatistics, proficiency in programming languages, and strong communication skills while promoting a culture of inclusiveness and collaboration

Job Summary

  • This role contributes to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions.
  • You will develop collaborative relationships and work effectively with the Biostatistics Lead and other cross-functional team members.
  • Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment and offers a wide variety of competitive benefits.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking a Manager of Biostatistics in Warsaw, Poland, to contribute to clinical trial design, analysis, and regulatory submissions. The role requires a fresh MS in statistics or biostatistics, proficiency in programming languages, and strong communication skills while promoting a culture of inclusiveness and collaboration.

Salary

Base: zł209,290 - zł253,607; Bonus/Equity: Additional incentive cash and stock opportunities may be available; Benefits: Competitive benefits, services and programs

Skills & Requirements

Must-have

  • clinical trial design
  • statistical analysis plan
  • SAS, R or Python programming
  • data manipulation and graphing
  • regulatory submissions

Nice-to-have

  • inclusive culture
  • respect for diversity
  • constructive challenging
  • scientific computing proficiency

Key Requirements

  • MS in statistics, biostatistics or related scientific field
  • Proficiency in scientific computing/programming
  • Good interpersonal, communication, writing and organizational skills
  • Ability to learn regulatory requirements & clinical trial design
  • Ability to work successfully within cross-functional teams

Work Rights

Not specified

Tailored Resume

Cover Letter