Jobs at CSL

Lead clinical trial case management for assigned studies, ensuring GxP and regulatory compliance. Oversee safety reporting plans, vendor performance, ICSR reporting, coding consistency, CAPAs and SOP projects, inspection readiness, and study-specific training. Act as PV subject-matter expert and liaison across functions and external collaborators to maintain timely, uniform safety data processing and regulatory submissions.

Lead day-to-day TMF operations across the portfolio: govern TMF processes, oversee eTMF systems (Veeva), manage vendors, ensure inspection readiness, track TMF KPIs, drive continuous improvement, and coach TMF staff.

Lead operational oversight for Process Science CI projects, ensuring timely delivery, cross-functional coordination (Manufacturing, QA, Regulatory, Supply Chain), risk identification, budget tracking, and stakeholder communication. Advise Process Science leadership, drive accountability, and support prioritization and continuous improvement within pharmaceutical development and manufacturing contexts.

Serve as the finance business partner to Legal and Corporate & External Affairs, providing FP&A, budgeting, forecasting, financial modeling, decision support, and cost management. Drive report automation and data visualization, advise leadership on financial risks and opportunities, and support enterprise technology spend optimization. Act as a trusted single point of contact for finance topics and deputy to the Director when needed.

Lead end-to-end site manufacturing for influenza vaccines, accountable for product quality, regulatory compliance (EMA/TGA/FDA), safety, budgets, capital projects, operational excellence, and cross-functional site leadership. Drive multi-year manufacturing strategy, LEAN/COS improvements, talent acquisition, inspection readiness, and supplier/partner relationships.

Provide high-quality executive and coordination support to Strategy & Corporate Development and Finance: manage external/internal meeting logistics, travel and visa arrangements, invoicing and expense reporting, prepare reports and presentations, liaise with senior stakeholders and counterparts globally, and support CFO and senior leaders with confidential diary and administrative tasks.

Partner with TechOps leadership to deliver financial planning, forecasting, modeling, KPI reporting, and decision support. Lead variance analysis, build dashboards, support business cases and strategic planning, drive continuous improvement, and ensure data integrity to optimize operational and financial performance.

Lead Portfolio Development operations as strategic partner to the SVP. Drive governance, cross-functional alignment, resource optimization, executive communications, and program execution to improve decision-making, portfolio efficiency, and leadership team performance in a matrixed biotech R&D environment.

Lead company secretariat and corporate governance for an ASX-listed global organisation. Advise the Board and Committees, oversee governance framework, continuous disclosure/ASX compliance, policy and entity management, support capital and remuneration matters, manage a small team, and partner with Legal and external stakeholders on regulatory, statutory and shareholder activities.

Manage end-to-end non-US/Central EU global labeling development and implementation. Assess labeling differences, lead exception reviews with the Global Labeling Committee, coordinate cross-functional stakeholders, resolve artwork/translation/supply issues, ensure CCDS-driven updates are communicated, represent Global Labeling in meetings, and maintain up-to-date global regulatory labeling compliance.

The role leads global efforts in procurement operations, focusing on risk management, supplier relationships, and process improvements, ensuring alignment with enterprise goals.

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.

The Accounts Receivable Analyst will manage collection and cash application activities, resolve payment issues, run reports, and ensure customer satisfaction. The role includes liaising with collection agencies and other teams, processing write-offs, and supporting improvement initiatives.

Lead enterprise value realization for I&T investments: shape business cases, track and forecast benefits, govern portfolio value delivery, report to executives, and partner with Finance and stakeholders to optimize ROI.

Lead establishment and maintenance of Portfolio Development processes, SOPs, training, and change initiatives. Drive process improvement, cross-functional programs, and procedural compliance to support clinical trial planning, evaluation, and reporting across global teams.

Lead end-to-end technical projects including technology transfers, lifecycle management, and continuous improvement. Develop and execute project plans, lead cross-functional teams and external CMOs/CDMOs, manage timelines, budgets, risks, KPIs and governance, perform technical due diligence and site assessments, and provide on-site manufacturing support.

The Associate Director, Federal Government Affairs will manage strategies for CSL Behring's federal interests, engage with stakeholders, provide policy insights, and collaborate on advocacy efforts.

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.

Prepare and review corporate tax returns, declarations, and reporting packages; analyze and interpret tax laws; maintain tax records; prepare correspondence with tax agencies and auditors; and coach less experienced staff as needed to ensure accurate, timely tax compliance.

The Senior Manager, Regional Regulatory Lead for Seqirus is responsible for regulatory strategies, health authority interactions, and managing regulatory activities for assigned vaccine products in North America.