Clinical Program Quality, Associate Director, R&D, China
About this role
About the Role Provides quality assurance oversight of the global and local clinical research programs in 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, offering risk-based quality expertise and guidance. Defines and implements a risk-based audit strategy and leads inspection readiness activities to communicate and mitigate quality risks to stakeholders and management.
Leads the inspection readiness programs, manages inspections, and coordinates response and follow-up actions. Ensures that inspection risks are communicated and mitigated for sponsor and investigator site inspections.
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