Teams at CSL

Supports regulatory strategy, product registrations, variation applications, lifecycle management, regulatory compliance, in-licensing due diligence, labeling, medicine shortages, inspections, audits, and stakeholder engagement for prescription medicines in Australia and New Zealand.

Lead statistical strategy and execution for clinical development programs. Oversee study design, SAP authoring, data analysis, TFL/CDISC deliverables, CRO/vendor oversight, regulatory interactions, and interpretation of results to support submissions and program decisions.

Leads clinical studies end to end, from protocol development and study start-up through execution, data interpretation, close-out, and clinical study reporting. Manages scientific deliverables and day-to-day CRO relationships within a full-outsourcing model, collaborates with clinical operations and cross-functional teams, and supports regulatory submissions and clinical data interpretation.