Description

• Champion patient-centric trial design and ethical decision-making, ensuring patient safety and data integrity are prioritized at all times.
• Drive strong cross-functional collaboration across Clinical science, Clinical Operation, Clinical Pharmacology, Biomarkers, Statistics, Regulatory, and other partners to enable integrated development strategies.
• Act as the China early development subject-matter expert in global governance forums, influencing development strategy and key portfolio decisions with local insights, clarity and credibility.
• Proactively identify scientific, clinical, and operational risks, demonstrating courage and ownership in addressing challenges, driving solutions, and balancing speed, quality, and value creation in line with Takeda’s long-term vision.
• Build trusted relationships with investigators, key opinion leaders, and external partners to support innovative early clinical research in China.
• Co...