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The Global Category Lead is responsible for developing and executing the strategy for external pharmaceutical manufacturing, focusing on sourcing, supplier management, and operational excellence while ensuring cost-effectiveness and compliance.

Lead coordination and execution of site contract and budget activities for clinical studies. Develop global templates, standards, and training; liaise with legal and data privacy; manage budgets, timelines, CRO resources, and metrics; support process improvements and ensure GCP/ICH and regulatory compliance.