Senior Global Trial Associate

Bristol Myers Squibb

Warsaw, Poland
Base: zł223,020 - zł270,251; bonus/equity: + incen...
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Knowledge of ich/gcp and regulatory guidelines
Experience with clinical trial management systems
Ability to manage study documentation and etmf
** 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 timely delivery. The ideal candidate will have 2-4 years of experience in clinical research, strong project management skills, and the ability to collaborate effectively within teams. **

Job Summary

  • The role contributes to the operational execution of clinical studies to ensure delivery on time, within budget, and in compliance with regulations.
  • Bristol Myers Squibb offers a wide variety of competitive benefits and programs that provide employees with resources to pursue goals at work and in personal lives.
  • Candidates will support the Global Trial Lead in ensuring eTMF accuracy, managing vendor activities, and tracking non-clinical supplies.

Matching Summary

Match Score: 75

** 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 timely delivery. The ideal candidate will have 2-4 years of experience in clinical research, strong project management skills, and the ability to collaborate effectively within teams. **

Salary

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

Skills & Requirements

Must-have

  • Knowledge of ICH/GCP and regulatory guidelines
  • Experience with Clinical Trial Management Systems
  • Ability to manage study documentation and eTMF
  • Vendor management and invoice approval skills
  • Risk identification and mitigation capabilities

Nice-to-have

  • Global clinical research experience preferred
  • Project management knowledge preferred
  • Mentoring and coaching team members
  • Process development and improvement initiatives
  • Strong cross-functional collaboration skills

Key Requirements

  • BA/BS in relevant discipline strongly preferred
  • Minimum 2-4 years' experience in Clinical Research
  • Experience with industry CTMS and CTMF systems

Work Rights

Not specified

Tailored Resume

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