Clinical Trial Manager
CSL
CSL is seeking an experienced Pharmacovigilance professional to act as a case management expert, ensuring regulatory compliance across multinational trials and safety data processing. The role involves managing safety reporting plans, overseeing vendor activities, and preparing for PV inspections within a GxP framework. You will maintain required PV documents, monitor KPIs, and contribute to process improvements and CAPA/SOP initiatives for timely regulatory reporting. #J-18808-Ljbffr
Vacancy posted 3 days ago
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