Principal Global Trial Associate

Bristol Myers Squibb UK

Warsaw, Poland
Base: zł239,890 - zł290,697; bonus/equity: + incen...
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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 clinical trials. The role involves project management, collaboration with cross-functional teams, and oversight of clinical trial processes to ensure compliance and quality. **

Job Summary

  • This role provides operational support for global interventional clinical trials from concept to final clinical study report, ensuring high-quality data generation.
  • The position involves managing project timelines, budgets, and risks while overseeing Contract Research Organizations (CROs) and internal stakeholders.
  • Bristol Myers Squibb offers a flexible work environment with opportunities to grow alongside high-achieving teams and access to competitive benefits.

Matching Summary

Match Score: 75

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

Salary

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

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
  • Cross-functional collaboration skills
  • Adaptability to changing priorities
  • Strategic thinking for study execution
  • Proactive risk identification and mitigation

Key Requirements

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

Work Rights

Not specified

Tailored Resume

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