The Opportunity: The Sr. Director, Head of Global Labeling Strategy leads the Global Labeling strategy function within Global Labeling, Advertising & Promotion and has overall responsibility for the worldwide labeling strategy portfolio within CSL. In this leadership position, the
Overview: The Manager, Clinical Trial Authorization (CTA) is responsible for ensuring that CTA activities for assigned clinical studies are planned, governed, and overseen in line with CSL regulatory expectations, quality standards, and development timelines. Reporting to
Quality Ownership & Purpose : You ensure robust quality control and quality assurance for sorbent materials and related QC processes in a dynamic scale‑up environment, delivering compliant, inspection‑ready outcomes and reliable product decisions within the QC
The Principal Clinical Data Oversight & Standards Lead provides leadership and oversight for clinical data build, programming, and vendor deliverables across in-house, hybrid, and outsourced studies, ensuring alignment with CSL standards, regulatory requirements, and industry best
The Director,Field EngagementIT Product Manageris avisionaryleader responsible forshaping and executing the strategy for enterprise-scale technology platforms that drive commercial and medical field effectiveness and engagement. Thisrole bridges business and technology, ensuring solutions deliver measurable value, support digital
Position Purpose The Associate Director, Statistical Programming provides leadership and expertise in driving the development and maintenance of the CSL statistical programming capabilities which is required to meet regulatory obligations. The individual will work closely with
