Manager

• Oversee the creation and maintenance of performance dashboards and reports to track KPIs across commercial functions like Pricing or Sales Operations
• Collaborate with cross-functional teams to ensure data needs are met and insights are communicated effectively to support decision-making
• Ensure data quality, governance, and integration from diverse internal and external sources for unified reporting
• Lead BI projects, managing timelines, deliverables, and alignment with business objectives
• Implement predictive analytics and advanced reporting techniques to provide actionable insights for business strategies
• Provide mentorship and guidance to BI team members, promoting continuous improvement and innovation in reporting practices
• Ensure compliance with regulatory requirements in all data management and reporting activities.

Manager, Global Reporting – Business Intelligence

Director

• Support implementation of value add, cost saving, productivity initiatives to maximize R&D investment
• Provide project leadership for such initiatives (matrix teams and FSP as needed)
• Lead continuous improvement initiatives for Cross-R&D business issues resolution team
• Business Partners Network to deliver the strategic initiatives selected by RDLT
• Oversee audit implementation, analysis and follow-up
• Coordinate BAR/AAR COE (Before and After-Action Reviews)
• R&D new training liaison

Associate Director, Continuous Improvement Initiatives – Process Management

Medical Billing and Coding

• Ensure implementation of GVP compliant PV standards, processes by the Pharmacovigilance Scientists, Device expert, and Medical coding expert under their management and conducts cross-functional collaboration with relevant individuals within PV as well as with key stakeholders
• PVS support for products in the post-marketing phase, as well as those products with ongoing clinical development as required
• Collaboration with Signal Management/Governance/Literature and Aggregate Reports/Risk Management Heads to support the work of PVS within the team, specifically in the contribution to signal detection and assessment activities through the full governance process, literature screening, and key contributions to aggregate reports, risk management plans, and other PVS-assigned responsibilities
• Utilization of managed service partners, ensuring on-time delivery of high-quality outputs assigned with implementation of meaningful KPI measures and regular reporting to senior management will be required
• Creating and implementing a vision which incorporates new technologies and innovative approaches will be essential to lead the team, while ensuring consistent support of the product-responsible GSLs.

Lead Post Marketing, Medical Coding, Device Safety PV Scientist

• Maximize Patient Access: Develop and implement strategies to ensure timely, equitable access to key products across all partner markets.
• Value and Access: Design and execute innovative pricing and reimbursement approaches tailored to local market needs, supporting business partners in building compelling value propositions for new launches and product lifecycle management.
• Partner Enablement: Equip business partners with the tools, insights, and support needed to optimize portfolio performance and navigate local access challenges.
• Cross-Functional Collaboration: Navigate effectively within the matrix, and act as a key connector between regional teams, International Brand Teams, Global Market Access and external partners to ensure alignment with global objectives and successful execution of access and pricing strategies.
• Market Intelligence: Monitor local healthcare environments, policy developments, and payer trends to identify opportunities and risks, sharing actionable insights across the partner network.
• Budget Management: Oversee budget allocation for the assigned portfolio, ensuring resources are used efficiently to support strategic objectives.
• Performance Measurement: Define and track key performance indicators to assess the impact of access and pricing initiatives.

Associate Director, Market Access

• Oversee the end-to-end management of the R&D digital portfolio, including project prioritization, resource allocation, and performance tracking to ensure timely delivery and alignment with organizational goals
• Collaborate with cross-functional teams, including R&D, IT, and data science, to ensure that digital initiatives align with strategic R&D goals and objectives
• Develop and maintain portfolio dashboards, KPIs, and reporting mechanisms to keep senior leadership informed of progress and performance
• Facilitate governance processes, including steering committees and investment reviews, ensuring clear decision-making and alignment on digital investments
• Identify risks, dependencies, and opportunities across the portfolio, and recommend mitigation strategies to ensure smooth execution of digital initiatives
• Support the R&D Digital Strategy and Delivery Lead in translating the strategic vision into executable programs, ensuring alignment with the overall digital roadmap
• Ensure consistent use of project management methodologies and tools (e.g., Agile, Waterfall) across all digital initiatives to standardize and optimize project execution

Associate Director, Digital Portfolio – Technology Enabled Science

Full-stack Engineer

• Responsible for the planning and execution of projects for evaluation, selection, improvement, and implementation of new or existing primary packaging materials, medical devices, and Combination Products for CSL products.
• Execution of projects within the agreed time, quality and cost constraints, resulting in state-of–the-art drug delivery devices.
• Collaborate with global internal cross-functional expert teams.
• Provide leadership to ensure the coordination of activities and information between the functions and with external partners.
• Application of expertise in Design Controls and Risk Management (ISO 13485, ISO 14971, and 21 CFR 820), EU MDR requirements, compilation and maintenance of Design History Files, design verification and validation, and clinical trial/commercial manufacture support.
• Provide leadership to Project Team to deliver submission-ready packages for Notified Bodies and regulators, as well as RFI responses.
• Utilise engineering and analysis tools to ensure robust designs and understand device limitations, (e.g., root cause analysis, tolerance analysis, probabilistic design).

Manager, Global Reporting – Business Intelligence

Associate Director, Continuous Improvement Initiatives – Process Management

Lead Post Marketing, Medical Coding, Device Safety PV Scientist

Associate Director, Market Access

Associate Director, Digital Portfolio – Technology Enabled Science

Senior Engineer, Drug Delivery Lead