Site Contract Specialist

Bristol Myers Squibb

Warsaw, Poland
Base: zł180,200 - zł218,360; bonus/equity: + incen...
Hybrid (50% onsite)
Bachelor's degree in life sciences or business administration
Experience in clinical trial contracting or operations
Strong attention to detail for contract documentation
Bristol Myers Squibb is seeking a Site Contract Specialist in Warsaw, Poland, to manage site contracting activities for clinical trials. The role emphasizes collaboration, negotiation, and operational excellence, offering opportunities for professional growth in a supportive company culture

Job Summary

  • The Site Contract Specialist plays a critical role in enabling clinical trials by supporting the preparation, negotiation, and finalization of site contracts and investigator budgets.
  • This position offers the opportunity to develop strong negotiation skills, build cross-functional partnerships, and gain exposure to clinical research operations within a regulated setting.
  • Bristol Myers Squibb recognizes the importance of balance and flexibility, offering competitive benefits and programs to help employees pursue their goals both at work and in their personal lives.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking a Site Contract Specialist in Warsaw, Poland, to manage site contracting activities for clinical trials. The role emphasizes collaboration, negotiation, and operational excellence, offering opportunities for professional growth in a supportive company culture.

Salary

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

Skills & Requirements

Must-have

  • Bachelor's degree in Life Sciences or Business Administration
  • Experience in clinical trial contracting or operations
  • Strong attention to detail for contract documentation
  • Proficiency with contract management systems
  • Effective communication in global multicultural environment

Nice-to-have

  • Experience supporting clinical studies
  • Familiarity with investigator grants and site budget negotiations
  • Experience with electronic document management systems
  • Structured problem-solving skills
  • Commitment to operational excellence and quality

Key Requirements

  • Bachelor's degree required
  • Prior experience in clinical trial contracting or pharmaceutical environment
  • Proficiency in MS Office tools

Work Rights

Not specified

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