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

Takeda

Full time Other Management Occupations
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Location
Shanghai, Shanghai, China
Posted
July 17, 2026

Job Description

Description

  • Provides quality assurance oversight of the global and local clinical research programs in Research and Development (R&D), Plasma Derived Therapy (PDT), Vaccines Business Unit (VBU), Oncology Business Unit (OBU), and Global Medical Marketed Products Development (MPD) with the overall goal of inspection readiness.
  • Serves as a Strategic Quality Thought Partner to Clinical Program Teams and other key stakeholders in the delivery of the clinical research programs, providing professional clinical research quality expertise and risk-based advice. 
  • Defines and implements a risk-based program audit strategy, ensuring the communication of significant quality and compliance risks to key stakeholders and Management, and ensuring appropriate and timely investigations and mitigations are in place
  • Leads the inspection readiness programs, the management of the inspection, and the response and follow-up activities. Ensures that inspection ri...

    • Job Details

    • Job Type
      Full time
    • Category
      Other Management Occupations
    • Date Posted
      July 17, 2026
    • Application Deadline
      August 26, 2026