Senior Manager, Biostatistics

Bristol Myers Squibb

50% onsite
Phd or master's in statistics
3+ years pharmaceutical experience
Clinical trial design expertise
The role involves contributing to trial design, protocol development, and interpretation of results for regulatory submissions

Job Summary

  • The role involves contributing to trial design, protocol development, and interpretation of results for regulatory submissions.
  • Employees will drive the design of innovative clinical trials that support regulatory approval and market access.
  • Bristol Myers Squibb offers a wide variety of competitive benefits and programs to support work-life balance.

Matching Summary

The role involves contributing to trial design, protocol development, and interpretation of results for regulatory submissions.

Skills & Requirements

Must-have

  • PhD or Master's in Statistics
  • 3+ years pharmaceutical experience
  • Clinical trial design expertise
  • Regulatory submission preparation
  • Cross-functional team collaboration

Nice-to-have

  • State-of-the-art statistical methodology
  • External reputation building skills
  • Cost-disciplined science approach
  • Conference participation experience

Key Requirements

  • PhD in statistics or biostatistics required
  • Master's degree with relevant experience accepted
  • Minimum 3 years in drug development
  • Understanding of biostatistics application to clinical data

Work Rights

Not specified

Tailored Resume

Cover Letter