Clinical Program Quality, Associate Director, R&D, China

This role provides quality assurance oversight for global clinical research programs in Takeda's R&D units, serving as a strategic thought partner to ensure inspection readiness and regulatory compliance. The incumbent defines risk-based audit strategies, leads health authority inspections, and manages supplier quality for outsourced non-clinical studies. Key duties include mentoring staff, investigating quality issues, and ensuring adherence to GCP and GLP regulations across various business units.