Job Summary

• Lead and manage matrix teams responsible for the end-to-end oversight of supply chain activities for investigational products across Phase I-IV protocols for both Small Molecule and Biologics programs.
• Design strategies that align with program, protocol, and regulatory requirements, identify and manage supply chain risk, manage multi-million clinical supply budgets, and provide guidance and leadership to the Clinical Supply Team.
• Act as the key Global Clinical Supply (GCS) point of contact for clinical study teams, Co-Development Teams (CDTs), asset teams, and Clinical Research Organizations (CROs) and represent GCS at the core study team.

Matching Summary

Salary

Base: $106,000.00 to $176,600.00; Bonus/Equity: 15.0% bonus target; Benefits: Comprehensive and generous benefits

Skills & Requirements

Key Requirements

• Bachelor's degree with at least 5 years of experience OR Master's degree with at least 3 years of experience OR PhD with 0+ years of experience OR Associate's degree with 8 years of experience OR High school diploma with 10 years of experience
• Demonstrated ability to manage large and complex clinical development programs
• Demonstrated knowledge and experience in GMP (cGMP) and GCP (GxP) environment
• Demonstrated understanding of pharma quality and regulatory framework
• Demonstrated in-depth experience managing multiple clinical studies in parallel
• Demonstrated experience leading and delivering in a matrix team environment
• Permanent work authorization in the United States

Work Rights