CBI - Biospecimen Lead (BSL)

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.

Responsibilities

• 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

Requirements

• 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

Compensation: zł218,900 - zł265,225