Associate Director, Clinical Trial Risk Lead

Bristol Myers Squibb

Warsaw, Poland
Base: zł357,560 - zł433,270; bonus/equity: + incen...
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8+ years pharmaceutical industry experience
5+ years clinical trial operations
Risk-based monitoring expertise
** Bristol Myers Squibb is seeking an Associate Director, Clinical Trial Risk Lead in Warsaw, Poland, to oversee risk management for clinical trials. The role involves implementing Quality by Design and Risk-Based Management principles to ensure trial integrity, requiring significant experience in clinical operations and data analysis. **

Job Summary

  • This role offers a rare chance to play an integral part in protecting the integrity of clinical trials and the patients who depend on them.
  • You will drive proactive risk management across a major clinical portfolio, owning the end-to-end process from protocol de-risking to lifecycle management.
  • Bristol Myers Squibb provides competitive benefits, services, and programs that support employees in pursuing their goals both at work and in their personal lives.

Matching Summary

Match Score: 75

** Bristol Myers Squibb is seeking an Associate Director, Clinical Trial Risk Lead in Warsaw, Poland, to oversee risk management for clinical trials. The role involves implementing Quality by Design and Risk-Based Management principles to ensure trial integrity, requiring significant experience in clinical operations and data analysis. **

Salary

Base: zł357,560 - zł433,270; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Wide variety of competitive benefits and programs

Skills & Requirements

Must-have

  • 8+ years pharmaceutical industry experience
  • 5+ years clinical trial operations
  • Risk-Based Monitoring expertise
  • Quality by Design principles
  • Statistical data analysis skills

Nice-to-have

  • Strategic thinking for senior leadership
  • Cross-functional collaboration abilities
  • Mentoring and coaching experience
  • External industry group representation
  • Data visualization proficiency

Key Requirements

  • Degree in Life Sciences, Data Science, Statistics, Analytics, or Business
  • Minimum 8 years in pharmaceutical industry
  • Minimum 5 years in clinical trial operations or GCP
  • Expertise in Risk Assessment & Control tools

Work Rights

Not specified

Tailored Resume

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