CBI - Biospecimen Lead (BSL)

Bristol Myers Squibb · Warsaw, Poland

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Role summary

Bristol Myers Squibb seeks a Biospecimen Lead to manage specimen protocols and operations across Phase 1-4 clinical trials. This independent contributor role coordinates with clinical teams to develop specimen management plans, track sample status, and ensure regulatory compliance while supporting 5-12 concurrent studies.

What they're looking for

4+ years experience in academic, biotech, healthcare, or pharmaceutical industry
Scientific degree (Associates, Bachelors, Masters, or higher) or equivalent project management experience
Intermediate knowledge of biospecimen procedures, collection, tracking, chain of custody, and data management
Intermediate vendor management experience with central labs, bioanalytical, or biospecimen storage providers
Basic understanding of GCP, GLP, CLIA, data management, and regulatory compliance
Effective communication and presentation skills; ability to train colleagues
Ability to manage 5-12 clinical trials of varying complexity with minimal supervision

What you'll be doing

Oversee biospecimen management across 5-12 clinical trials with independent decision-making authority
Develop specimen management plans that identify risks and mitigation strategies for regulatory compliance
Track and reconcile biospecimen status using internal and external systems; provide regular updates to clinical teams
Coordinate with vendors and clinical teams to resolve biospecimen issues and participate in vendor audits
Maintain study documentation in inspection-ready condition and contribute to cross-functional workflow optimization projects

Compensationzł218,900 - zł265,225

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