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Clinical Supply Specialist

Qualifications
Minimum Work Experience:
Experience in clinical logistics, or related field within the biopharmaceutical industry or in general logistics
Project Management experience.
Individuals should have a strong understanding of cross functional activities
Demonstrated multinational work experience.
Fluent in English
Education:
Bachelor's degree, or equivalent (e.g. Pharm. D.), in biology, pharmacy or other health-related discipline, international trade or logistics business.
Job Description
PAREXEL's Clinical Logistics Services group uses industry-leading supply chain intelligence, developed through the unique combination of PAREXEL expertise and our state-of-the-art eClinical and eLogistics solutions. This intelligence is dynamically used throughout the process, to anticipate issues, develop solutions and implement actions that optimize supply levels, reduce costs to clients, and enhance future trials by tightly integrating with the entire trial. PAREXEL delivers beginning-to-end clinical logistics management by lowering costs and improving compliance and efficiency in all aspects of the clinical trial process.
The CSS supports the Clinical Trial Supply and Logistics teams by applying and executing supply chain to achieve client satisfaction and delivery of projects /programs on time, to budget, to the highest quality and in compliance with applicable ICH-GxP and other applicable local regulation and industry guidelines. The CSS has responsibility for the execution of the clinical trial supply logistics strategy on the project.


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