Director

• You will be accountable for the design and execution of the clinical strategy to support the development of a medicine, aligned with the Project Strategy Document (PSD) and the Target Product Profile (TPP).
• You are also accountable for the strategic leadership of the Clinical Development Team (CDT) in a matrix environment and is responsible for: the timely development and execution of the Clinical Development Plan (CDP).
• Managing the day-to-day operations of the CDT including but not limited to meeting coordination and documentation, decision making, and stakeholder management.
• Ensuring that the program is conducted in alignment with CSL Behring processes and abiding by GCP and ICH regulations.
• This position is accountable for the clinical & scientific oversight of the assigned program(s) and: ensures high quality clinical & scientific standards are met during all aspects of the program providing clinical oversight and expertise during development of clinical studies.

Senior Director, Global Clinical Program Lead – Cardiovascular, Renal

• Lead the development, design, governance, implementation and continuous improvement of required Project Management Tools, Templates and standards for R&D to enable consistent, compliant, and high-quality project delivery across the R&D portfolio
• Design, develop, systematize and maintain a standardized suite of required tools, templates and supportive frameworks for R&D Project Management excellence
• Update and refine tools and templates using AI and digital technologies/solutions
• Key customer lead for development and continued improvement of Tools and Templates
• Gather regular user feedback and performance data to assess effectiveness and usability of tools and templates
• Liaise with Continuous Improvement & Process Management Leads to ensure that Tools & Templates support and are aligned with R&D and PM processes, portfolio and project governance forums
• Liaise with GPLs, PMs, PSTs, TA Delivery Leads and Functional representatives to embed best practices, regulatory expectations and operational excellence into day-to-day project execution
• Lead liaison with Technology Enabling Support (TES) for digital solution development and platform optimization
• Drive adoption and consistent use of tools and templates across the R&D organization
• Provide clear guidance on when and how to use tools across different project contexts supporting capability-building initiatives through workshops, training sessions, and communities of practice
• Monitor external trends, digital solutions and emerging best practices to modernize tools and ways of working

Associate Director, Tools & Templates, R&D Performance Management Office

Manager

• Establish and maintain relationships with the key business and technology stakeholders
• Collaborate with business partners to understand needs and define solution outcomes
• Identify and scale new digital products that align with market and organizational goals
• Monitor and apply emerging technologies to enhance existing solutions
• Contribute to the creation of roadmaps of prioritized future capabilities for their solution/product domain
• Serve as a subject matter expert and solution authority within the product domain
• Lead cross-functional teams to deliver solutions on time and within governance frameworks
• Proactively address technical issues, reduce technical debt, and harmonize architecture
• Apply technical knowledge, including agile practices, to solve business problems
• Prepares activity and progress reports regarding applications, systems operations programming and project activities for area of responsibility
• Ensure compliance with regulatory, security, and enterprise standards
• Manages lifecycle management activities of solution/product in line with enterprise application processes and non-functional roadmaps

Senior Manager, I&T Plasma Digital Products

• Responsible for defining, implementing, and maintaining data standards and governance frameworks across research and laboratory environments
• This role ensures high-quality, interoperable, and FAIR (Findable, Accessible, Interoperable, Reusable) data to support scientific discovery, digital innovation, and regulatory readiness
• Develop and maintain data standards for research and lab-generated data, such as assay data, instrument outputs, and metadata, ensuring consistency across platforms and teams
• Establish governance frameworks to ensure consistent data capture, annotation, and integration across digital systems (e.g., ELNs, LIMS, data lakes)
• Collaborate with scientists, lab managers, IT, and data stewards to embed data standards into lab workflows and digital systems, supporting seamless data integration and usage
• Monitor compliance with established data standards, identifying opportunities for improvement and driving continuous quality enhancements
• Represent the organization in external data standards bodies and consortia (e.g., Allotrope, FAIR sharing, Pistoia Alliance) to ensure alignment with global data standards and best practices
• Support data quality, lineage, and traceability efforts, enabling the use of data for advanced analytics, AI/ML applications, and regulatory submissions
• Provide training, guidance, and support to internal teams on data standards, ontologies, and governance best practices to ensure consistent adoption across the organization.

Director, Research & Labs, Data Standards and Excellence

Clinical Research

• The statistician contributes to components of study design, e.g. sample size calculations
• Significant role in planning the analyses of a clinical trial (e.g. author the SAP; define table shells; programming specs)
• Responsible for the quality and timely delivery of interim and final results

Senior Director, Global Clinical Program Lead – Cardiovascular, Renal

Associate Director, Tools & Templates, R&D Performance Management Office

Senior Manager, I&T Plasma Digital Products

Director, Research & Labs, Data Standards and Excellence

Senior Biostatistician