Job Summary

• You'll partner closely with the PRC Lead and cross-functional teams to ensure the seamless execution of protocol review activities across multiple Therapeutic Areas (TAs).
• Your key responsibilities include owning the end-to-end PRC process from scheduling and documentation through to compliance tracking, partnering with the PRC Lead to manage submissions across multiple TAs.
• Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.

Matching Summary

Salary

Base: zł162,000 - zł196,318; Bonus/Equity: Additional incentive cash and stock opportunities may be available; Benefits: Competitive benefits, services and programs

Skills & Requirements

Key Requirements

• 5+ years in clinical research
• Bachelor's degree preferred
• Conceptual knowledge of protocol design
• Foundational understanding of GCP principles
• Proficiency in Microsoft Office

Work Rights