Global Clinical Supply Chain Manager

2 months ago


Maidenhead, Windsor and Maidenhead, United Kingdom CSL Full time

Job Summary

The Senior Director Clinical Trial Supply Chain is responsible for leading the development and implementation of clinical trial supply chain strategies to ensure timely and cost-effective delivery of clinical supplies to study sites.

Key Responsibilities

  • Provide strategic leadership and direction to the clinical trial supply chain team to ensure alignment with business objectives.
  • Develop and implement clinical trial supply chain strategies to optimize supply chain efficiency, reduce costs, and improve quality.
  • Collaborate with cross-functional teams, including Clinical R&D, Manufacturing, and Quality Assurance, to ensure seamless supply chain operations.
  • Manage and negotiate contracts with clinical supply vendors to ensure performance relative to key performance indicators (KPIs).
  • Develop and maintain relationships with key stakeholders, including study site personnel, to ensure effective communication and issue resolution.
  • Ensure compliance with regulatory requirements, including Good Clinical Practices (GCP) and Good Manufacturing Practices (GMP).
  • Drive continuous improvements in clinical trial supply chain processes and systems to ensure optimal use of resources and minimize waste.

Requirements

  • University degree in life sciences, engineering, logistics, or equivalent experience.
  • 12+ years' pharmaceutical or clinical experience related to clinical or operational supply.
  • 5+ years' experience in clinical drug supply in the pharmaceutical industry with global responsibility.
  • Demonstrated leadership experience.
  • Strong knowledge and experience in GCP/GMP principles and relevant international standards and regulatory requirements.
  • Fluent English skills.
  • Willing to travel approximately 20% of the time.


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