Senior Global Trial Associate

Bristol Myers Squibb

Warsaw, Poland
Base: zł223,020 - zł270,251; bonus/equity: + incen...
Hybrid (50% onsite)
Knowledge of ich/gcp regulations
Experience with clinical trial management systems
Study level documentation management
Bristol Myers Squibb is seeking a Senior Global Trial Associate in Warsaw, Poland, to contribute to the operational execution of clinical studies, ensuring compliance with regulations and quality standards. The role involves project management, collaboration with stakeholders, and oversight of study deliverables, offering a dynamic work environment focused on meaningful advancements in patient care

Job Summary

  • The role involves contributing to the operational execution of clinical studies to ensure delivery on time, within budget, and of high quality.
  • Employees will manage study-level documentation, support eTMF accuracy, and assist in vendor management activities under moderate supervision.
  • Bristol Myers Squibb offers a wide variety of competitive benefits and programs to help employees pursue goals both at work and in their personal lives.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking a Senior Global Trial Associate in Warsaw, Poland, to contribute to the operational execution of clinical studies, ensuring compliance with regulations and quality standards. The role involves project management, collaboration with stakeholders, and oversight of study deliverables, offering a dynamic work environment focused on meaningful advancements in patient care.

Salary

Base: zł223,020 - zł270,251; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Wide variety of competitive benefits and programs provided

Skills & Requirements

Must-have

  • Knowledge of ICH/GCP regulations
  • Experience with Clinical Trial Management Systems
  • Study level documentation management
  • Vendor invoice review and approval
  • eTMF accuracy and completion support

Nice-to-have

  • Global experience in clinical research
  • Mentoring junior team members
  • Process development and improvement skills
  • Cross-functional collaboration abilities
  • Challenging the status quo mindset

Key Requirements

  • BA/BS in relevant discipline strongly preferred
  • Minimum 2-4 years' experience in Clinical Research
  • Working knowledge of project management preferred

Work Rights

Not specified

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