Clinical Trial Manager

Bristol Myers Squibb

Warsaw, Poland
Base: zł223,020 - zł270,251; bonus/equity: + incen...
On-site
End-to-end study operational oversight
Country level study delivery
Adherence to timelines, budget, quality
Bristol Myers Squibb is seeking a Clinical Trial Manager based in Warsaw, Poland, responsible for overseeing clinical study operations and ensuring compliance with timelines, budgets, and quality standards. The ideal candidate will have a background in life sciences, with at least four years of relevant industry experience and a strong understanding of clinical research regulations

Job Summary

  • The Clinical Trial Manager is accountable for end-to-end study operational oversight and delivery at country level, overseeing several studies conducted across multiple countries.
  • Key responsibilities include implementing local country and site feasibility, planning and executing timelines, managing patient recruitment strategies, and ensuring data integrity in CTMS, eDC, and eTMF systems.
  • Bristol Myers Squibb offers a work environment that transforms lives, with opportunities for growth and a wide variety of competitive benefits.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking a Clinical Trial Manager based in Warsaw, Poland, responsible for overseeing clinical study operations and ensuring compliance with timelines, budgets, and quality standards. The ideal candidate will have a background in life sciences, with at least four years of relevant industry experience and a strong understanding of clinical research regulations.

Salary

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

Skills & Requirements

Must-have

  • End-to-end study operational oversight
  • Country level study delivery
  • Adherence to timelines, budget, quality
  • Vendor assessment and setup
  • CTMS, eDC, eTMF software proficiency
  • GCP, ICH Guidelines knowledge

Nice-to-have

  • Patient recruitment strategy
  • Risk mitigation and problem-solving
  • Inspection readiness
  • Corrective Actions / Preventive Actions (CAPA)
  • Health Authority submissions

Key Requirements

  • Bachelor's or Master's degree in life sciences or equivalent
  • Minimum of 4 years' industry related experience
  • Experience in leading cross-functional teams
  • Knowledge of clinical research processes and regulations

Work Rights

Not specified

Tailored Resume

Cover Letter