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The role involves leading statistical programming for clinical studies, ensuring compliance with CDISC standards, collaborating across teams, and enhancing programming efficiency through automation.

The Associate Director, Trial Master File oversees eTMF governance for clinical trials, ensuring compliance, quality, and timeliness in processes to support inspections and collaboration across functions.

The Sr. Director of Commercial Supply Chain leads supply chain operations, ensuring steady drug supply, demand forecasting, and cross-functional collaboration for clinical and commercial programs.

The Associate Director, Legal Counsel will provide comprehensive legal support in R&D activities, manage contracts, mitigate legal risks, and ensure compliance with laws and regulations in mainland China.

The Associate Director, Program Management will manage late-stage clinical programs, ensuring timelines, budgets, and regulatory compliance are met while facilitating cross-functional collaboration.