Global Clinical Supply Chain Manager
2 months ago
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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