Global Trial Associate

Bristol Myers Squibb

Warsaw, Poland
Base: zł180,200 - zł218,360 annually; bonus/equity...
50% onsite
End-to-end clinical trial execution
Vendor oversight and invoice management
Study documentation and etmf accuracy
Bristol Myers Squibb is seeking a Global Trial Associate based in Warsaw, Poland, to support the execution of clinical trials, ensuring they are completed on time and within budget. The role involves project management, vendor oversight, and collaboration with cross-functional teams. Candidates should have a background in clinical research and a strong understanding of regulatory guidelines

Job Summary

  • This role plays a key part in driving the end-to-end execution of clinical trials to ensure they are delivered on time, on budget, and to the highest quality standards.
  • The position involves managing critical study documentation, vendor oversight, and CTMS milestones while partnering with the Global Trial Lead and key stakeholders.
  • Bristol Myers Squibb offers a wide variety of competitive benefits and programs designed to support employees in pursuing their goals both at work and in their personal lives.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking a Global Trial Associate based in Warsaw, Poland, to support the execution of clinical trials, ensuring they are completed on time and within budget. The role involves project management, vendor oversight, and collaboration with cross-functional teams. Candidates should have a background in clinical research and a strong understanding of regulatory guidelines.

Salary

Base: zł180,200 - zł218,360 annually; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Wide variety of competitive benefits and programs provided

Skills & Requirements

Must-have

  • End-to-end clinical trial execution
  • Vendor oversight and invoice management
  • Study documentation and eTMF accuracy
  • Cross-functional team collaboration
  • Risk identification and mitigation

Nice-to-have

  • Willingness to challenge the status quo
  • Proactive contribution to business demands
  • Global experience in clinical research
  • Strong oral and written communication skills

Key Requirements

  • BA/BSc or associate degree in relevant discipline
  • 2-4 years of experience with Clinical Trial Management Systems
  • Knowledge of ICH/GCP and regulatory guidelines
  • Experience in Clinical Research or related work

Work Rights

Not specified

Tailored Resume

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