Principal Global Trial Associate

Bristol Myers Squibb

Warsaw, Poland
Base: zł239,890 - zł290,697; bonus/equity: + incen...
Hybrid (50% onsite)
4-6 years clinical research experience
Knowledge of ich/gcp regulatory guidelines
Experience with ctms and etmf systems
Bristol Myers Squibb is seeking a Principal Global Trial Associate in Warsaw, Poland, to provide operational support for interventional clinical trials. The role involves project management, oversight of study deliverables, and collaboration with cross-functional teams to ensure successful trial execution

Job Summary

  • This role provides operational support for global interventional clinical trials from concept to final clinical study report.
  • The position involves managing project timelines, budgets, and risks while overseeing Contract Research Organization teams.
  • Bristol Myers Squibb offers a flexible work environment with opportunities to work remotely up to 50% of the time.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking a Principal Global Trial Associate in Warsaw, Poland, to provide operational support for interventional clinical trials. The role involves project management, oversight of study deliverables, and collaboration with cross-functional teams to ensure successful trial execution.

Salary

Base: zł239,890 - zł290,697; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Wide variety of competitive benefits and programs

Skills & Requirements

Must-have

  • 4-6 years clinical research experience
  • Knowledge of ICH/GCP regulatory guidelines
  • Experience with CTMS and eTMF systems
  • Project management in pharmaceutical industry
  • Vendor and CRO oversight capabilities

Nice-to-have

  • Mentoring junior Global Trial Associates
  • Adaptability to changing business demands
  • Cross-functional collaboration skills
  • Proactive risk identification and mitigation
  • Strategic thinking in study execution

Key Requirements

  • BA/BS degree in relevant discipline
  • Minimum 4-6 years of global study operations experience
  • Moderate familiarity with global regulatory landscape

Work Rights

Not specified

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