Manager, Biospecimen Management

Bristol Myers Squibb UK

Not specified; not specified; competitive benefits...
Hybrid (50% onsite)
Oversee biospecimen management in 5-12 clinical trials
Develop specimen management plan with risk mitigation
Track and reconcile biospecimen status using systems
Bristol Myers Squibb is seeking a Manager of Biospecimen Management to oversee biospecimen activities in clinical trials. The role involves developing management plans, ensuring regulatory compliance, and acting as a liaison between clinical teams and vendors

Job Summary

  • The role involves overseeing biospecimen management across 5-12 clinical trials with minimal supervision while ensuring operational feasibility and regulatory compliance.
  • Employees will act as a liaison between clinical teams and vendors to resolve issues, participate in audits, and maintain inspection-ready study documents.
  • Bristol Myers Squibb offers a supportive culture with competitive benefits, flexibility, and opportunities to work on life-changing science alongside high-achieving teams.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking a Manager of Biospecimen Management to oversee biospecimen activities in clinical trials. The role involves developing management plans, ensuring regulatory compliance, and acting as a liaison between clinical teams and vendors.

Salary

Not specified; Not specified; Competitive benefits and programs provided

Skills & Requirements

Must-have

  • Oversee biospecimen management in 5-12 clinical trials
  • Develop Specimen Management Plan with risk mitigation
  • Track and reconcile biospecimen status using systems
  • Coordinate between clinical teams and external vendors
  • Participate in vendor audits and CAPA resolutions

Nice-to-have

  • Experience optimizing workflows and integrating technology
  • Ability to provide training and mentorship
  • Intermediate knowledge of therapeutic area requirements
  • Strong communication skills for cross-functional projects

Key Requirements

  • Experience managing biospecimens in clinical trials
  • Knowledge of standard operating procedures and guidance documents
  • Ability to enter requirements into contracting systems
  • Proficiency in tracking inventory and quality issues

Work Rights

Not specified

Tailored Resume

Cover Letter