Global Trial Associate

Bristol Myers Squibb

Warsaw, Poland
Base: zł180,200 - zł218,360; bonus/equity: + incen...
50% onsite
Clinical trial management systems (ctms)
Etmf accuracy and completion
Vendor invoice approval process
This role plays a key role in driving the end-to-end execution of clinical trials, ensuring they are delivered on time, on budget, and to the highest quality standards

Job Summary

  • This role plays a key role in driving the end-to-end execution of clinical trials, ensuring they are delivered on time, on budget, and to the highest quality standards.
  • Responsibilities include managing critical study documentation, vendor oversight, and CTMS milestones, with opportunities for growth and development.
  • Bristol Myers Squibb offers a wide variety of competitive benefits, services, and programs that provide employees with resources to pursue their goals both at work and in their personal lives.

Matching Summary

This role plays a key role in driving the end-to-end execution of clinical trials, ensuring they are delivered on time, on budget, and to the highest quality standards.

Salary

Base: zł180,200 - zł218,360; Bonus/Equity: Additional incentive cash and stock opportunities may be available; Benefits: Competitive benefits, services and programs

Skills & Requirements

Must-have

  • Clinical Trial Management Systems (CTMS)
  • eTMF accuracy and completion
  • Vendor invoice approval process
  • ICH/GCP and regulatory guidelines
  • Study documentation management
  • Cross-functional team collaboration

Nice-to-have

  • Proactive contribution to business demands
  • Willingness to challenge status quo
  • Networking with key stakeholders
  • Flexibility to changing business demands

Key Requirements

  • BA/BSc or associate degrees
  • 2-4 yrs CTMS/eTMF experience
  • Clinical Research experience
  • Global experience

Work Rights

Not specified

Tailored Resume

Cover Letter