Jobs 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.

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.

Supports Japan finance leadership through business partnering, financial analysis, budgeting, forecasting, variance analysis, KPI reporting, dashboards, and executive presentations. Coordinates financial inputs across markets and FP&A teams, maintains data quality, improves reporting processes, and provides insights for commercial decisions, risks, opportunities, product launches, and other initiatives. Builds stakeholder relationships across Finance and Commercial teams.

Provide strategic, actionable employment and industrial relations legal advice across APAC, with primary responsibility for Australian matters. Advise on disputes, restructures, investigations, terminations, compliance, enterprise agreements, union consultations, and collective disputes. Manage regional employment-law matters, oversee external counsel, and represent CSL in litigation and agency proceedings while partnering with HR, risk, compliance, and business teams.

Supports CSL’s sales and marketing teams through commercial operations administration, systems coordination, compliance reporting, contract maintenance, financial processing, onboarding, IT device coordination, meetings, travel, and customer event logistics. The role requires strong Microsoft Office skills, organization, accuracy, stakeholder management, confidentiality, and the ability to prioritize multiple deadlines in a corporate or pharmaceutical environment.

Manage accurate and compliant Japan payroll operations, including employee inquiries, social insurance, benefits, retirement payments, PTO, attendance, overtime, vendor processing, statutory reporting, and payroll data in Workday. Coordinate with HR, Finance, Benefits, vendors, employees, and government agencies. Support audits, reporting, forecasting, payroll accounting, process improvements, and system or vendor transitions.

Leads regulatory affairs operations and strategy across Australia and New Zealand for CSL. Oversees product registrations, lifecycle management, regulatory submissions, labeling, promotional review, compliance, audit readiness, and CAPA completion. Acts as the primary interface with health authorities, government bodies, industry associations, and commercial teams while guiding regulatory teams and managing complex cross-functional timelines.

Lead global vaccines safety science activities including pharmacovigilance governance, regulatory compliance, signal detection, safety data analysis, inspection readiness, PSMF maintenance, process optimization, and technical translation of business requirements into reporting and visualization solutions. Manage teams, contribute to post-marketing and study safety reporting, and support regulatory submissions and audits.

Lead global labelling strategy and operations for Seqirus' vaccine portfolio, manage and coach a global labelling team, own end-to-end labelling review and approval, ensure regulatory compliance and timely safety updates, support annual strain updates, represent company in regulatory forums and audits, and collaborate cross-functionally to deliver timely labelling.

Leads Japan-focused regulatory CMC strategy for biopharmaceutical products, including regulatory filings, health authority interactions with PMDA and MHLW, submission management, lifecycle activities, compliance, risk assessment, and cross-functional collaboration. Provides strategic guidance, mentors colleagues, maintains regulatory records, and supports product development, registration, commercialization, and continuous process improvement.

Serve as CSL's senior representative in the regional biotech ecosystem to source and evaluate external innovation, build executive partnerships, support regional BD/licensing transactions end-to-end, provide market intelligence, and represent CSL at industry and government forums to shape strategic pipeline opportunities.