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.

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.

Leads translational research and preclinical development for CSL Behring’s immunology portfolio. Designs in vitro and ex vivo studies, develops pharmacodynamic and biomarker strategies, supports toxicology and early clinical studies, and collaborates with pharmacology, clinical development, CRO, and internal teams. Responsibilities include preparing research plans, regulatory and clinical documents, supporting indication selection and due diligence, aligning projects with therapeutic-area strategy, and building external scientific networks.

Provides legal counsel across EMEA for commercial contracts, pharmaceutical manufacturing, employment matters, corporate governance, compliance, regulatory issues, and third-party disputes. Leads contract template harmonization, process optimization, and contracting initiatives while partnering with commercial, medical, regulatory, procurement, compliance, and business stakeholders. The role is hybrid, requiring three office days weekly.

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.

Leads project management for biotech due diligence and external innovation activities, including in-licensing and partnership evaluations. Develops integrated plans, timelines, budgets, risk tracking, governance tools, dashboards, and decision-support materials. Coordinates scientific, clinical, regulatory, legal, IP, commercial, and finance stakeholders; ensures timely, compliant evaluations; supports senior leadership decisions; and improves due diligence workflows and tools. The role also mentors junior team members and manages relationships with external partners.

Leads strategic international communications for CSL’s Commercial & Medical business across 39 countries. Responsibilities include advising senior executives, developing communications strategy, managing crisis and reputational issues, directing internal communications, supporting brands and therapeutic areas, and leading a global communications team. The role requires extensive communications experience in a regulated industry and includes approximately 15% pan-European travel.

Perform and review financial accounting activities for multiple entities, including journal entries, accruals, reconciliations, statutory reporting, budgeting, forecasting, variance analysis, IFRS compliance, and audit support. The role also resolves SAP and FinanceCore transaction issues, supports continuous improvement projects, and liaises with finance business partners and auditors. This is a hybrid position requiring three office days per week in Speke, Liverpool.

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.

Coordinates accounting and month-end close activities across multiple countries, including journal preparation, reconciliations, financial reporting, audit support, internal controls, statutory compliance, and variance analysis. The role applies technical accounting knowledge, supports tax and treasury processes, manages ERP interfaces, identifies control improvements, and collaborates with finance teams on balance sheet planning and group consolidation.

Supports intercompany accounting processes, including invoices, recharges, payments, journals, reconciliations, reporting, netting, and mismatch investigations. Maintains intercompany mailboxes, responds to auditor queries, addresses billing and pricing issues, assists with forecasting and budgeting, and contributes to continuous improvement projects. The hybrid role requires three office days per week in Speke, Liverpool.

Provides high-level support to the General Manager while coordinating calendars, meetings, travel, communications, stakeholders, onboarding, suppliers, office services, employee initiatives, and compliance administration. The role also supports executive materials, health and safety processes, events, and improvements to administrative workflows and employee experience.

Lead epidemiology strategy and programs for assigned products, design and execute studies, manage data and vendors, contribute to regulatory submissions, drive RWE use, perform benefit-risk assessments, and support departmental process improvement and cross-functional leadership.

Leads global clinical development strategy and execution for hematology programs, guiding 5–8 Global Clinical Program Leaders and representing Clinical Development on therapeutic area leadership teams. Oversees clinical plans, protocol design, regulatory submissions, benefit-risk assessments, business development support, and interactions with health authorities, payers, commercial teams, physicians, and external experts. Mentors clinical drug developers, supports matrix collaboration, engages key opinion leaders, and drives scientific and operational excellence across the portfolio.

Manages accounts payable processes and master data for the EMEA region, including invoice processing, payment-run approval, supplier issue resolution, WE/RE account reconciliation, KPI monitoring, audit support, and coordination with external service providers. The role also handles tax and commercial-law compliance, process improvements, master-data approvals, and subproject responsibilities. Requires accounting expertise, SAP FI/CO knowledge, and several years of accounts payable experience.

Provides strategic and hands-on biostatistical leadership across pharmaceutical discovery, translational, biomarker, and early research programs. Designs studies, analyzes complex biological datasets, develops advanced statistical methods and reproducible R workflows, and translates evidence into portfolio decisions. The role collaborates with quantitative and scientific functions, supports publications and external partnerships, mentors statisticians, and advances data-driven analytical practices.

Drafts, reviews, and negotiates commercial agreements throughout the contracting lifecycle. Maintains contract templates, FAQs, and CLM records; advises business partners on legal matters; delivers training; and identifies opportunities to improve legal service efficiency through process optimization, automation, legal design, and technology. The role collaborates across departments and may require occasional domestic or international travel.

Drafts, reviews, negotiates, and manages commercial agreements across EMEA. Provides risk-based legal advice, supports contract lifecycle activities, develops templates and playbooks, trains stakeholders, and improves contracting through automation, legal technology, CLM tools, and AI-enabled solutions. The role collaborates with legal and business teams across multiple jurisdictions and cultures.