Job Summary

• Lead and manage matrix teams responsible for the end-to-end oversight of supply chain activities for investigational product on phase I-IV protocols.
• Responsible for designing strategies that align with program, protocol, and regulatory requirements, identifying and managing supply chain risk, and managing multi-million clinical supply budgets.
• Act as the key Global Clinical Supply (GCS) point of contact for clinical study teams and represent GCS at the core study team.

Matching Summary

Salary

Base: $106,000.00 - $176,600.00; Bonus/Equity: 15.0% bonus target; Benefits: Comprehensive and generous benefits package including 401(k), paid time off, and health benefits

Skills & Requirements

Key Requirements

• Bachelor's degree with 5 years of experience OR Master's degree with 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 working in a GMP/GCP environment
• Demonstrated in-depth experience managing multiple clinical studies in parallel
• Permanent work authorization in the United States

Work Rights