Senior Global Trial Operations Lead

Bristol-Myers Squibb

Warszawa

Hybrid

PLN 240,000 - 291,000

Full time

14 days+
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Benefits offered by this job

Hybrid work model
Remote work option

Job summary

Bristol Myers Squibb in Warsaw, Poland seeks a Principal Global Trial Associate to independently manage global clinical trial deliverables across lifecycle stages. The role emphasizes compliance, risk management, and timely milestone delivery in collaboration with CROs and cross-functional teams.

The ideal candidate holds a scientific/healthcare degree with 4–6+ years in trial operations, strong ICH-GCP knowledge, and a track record of mentoring and process improvement.

Qualifications

  • Bachelor's degree in a scientific, healthcare, or related discipline.
  • 4–6+ years of experience in clinical trial operations or global study management.
  • Experience managing operational deliverables across global clinical trials.
  • Strong understanding of ICH-GCP and clinical trial regulations.
  • Experience as SME, mentor, or process improvement lead valued.

Responsibilities

  • Independently manage complex study deliverables and operational activities.
  • Drive inspection readiness, compliance activities, and quality oversight.
  • Oversee study documentation, eTMF quality, and milestone tracking.
  • Support vendor oversight, budget management, and financial reconciliation.
  • Partner with Global Trial Leads to resolve challenges.
  • Lead initiatives to improve study execution and efficiency.

Skills

Clinical operations
Global study management
Vendor management
Mentoring
ICH-GCP knowledge

Education

Bachelor's degree
Life sciences

Tools

ETMF

Job description

Bristol Myers Squibb in Warsaw, Poland seeks a Principal Global Trial Associate to independently manage global clinical trial deliverables across lifecycle stages. The role emphasizes compliance, risk management, and timely milestone delivery in collaboration with CROs and cross-functional teams.

The ideal candidate holds a scientific/healthcare degree with 4–6+ years in trial operations, strong ICH-GCP knowledge, and a track record of mentoring and process improvement.

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