Manager, Supply Chain Lead (scl)

pfizer.hu

Base: $106,000.00 - $176,600.00; bonus/equity: 15....
Hybrid
Clinical study design and drug supply processes
End-to-end oversight of supply chain activities
Investigational product strategies
Lead and manage matrix teams responsible for the end-to-end oversight of supply chain activities required for the provision of investigational product

Job Summary

  • Lead and manage matrix teams responsible for the end-to-end oversight of supply chain activities required for the provision of investigational product.
  • Responsible for designing strategies that align with program, protocol, and regulatory requirements, identifying and managing supply chain risk, managing multi-million clinical supply budgets, and providing guidance and leadership to the Clinical Supply Team (CST).
  • The SCL is 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 represents GCS at the core study team.

Matching Summary

Lead and manage matrix teams responsible for the end-to-end oversight of supply chain activities required for the provision of investigational product.

Salary

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

Skills & Requirements

Must-have

  • Clinical study design and drug supply processes
  • End-to-end oversight of supply chain activities
  • Investigational product strategies
  • Clinical supply budgets management
  • Supply chain risk identification and management
  • Global Clinical Supply (GCS) point of contact

Nice-to-have

  • Innovative solutions for drug supply
  • Continuous Improvement projects participation
  • Leadership and coaching capabilities

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 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

Permanent work authorization required

Tailored Resume

Cover Letter