Telix Pharmaceuticals Limited

• Build and operationalize foundational global trade compliance processes, controls, and procedures. • Ensure compliance with international trade regulations, customs requirements, import/export controls, sanctions programs, and country-specific permitting requirements. • Partner closely with Supply Chain, Manufacturing, Regulatory Affairs, Quality, Clinical Operations, Logistics, Procurement, Finance, Legal, and Commercial teams. • Lead internal trade compliance reviews, investigations, and corrective action plans. • Develop and maintain the company’s global Harmonized Tariff Schedule (HTS) classification framework. • Coordinate and manage day-to-day Importer of Record (IOR) and Exporter of Record requirements globally. • Identify and administer duty drawback and duty optimization processes.

• Acts as the primary point of contact for Telix Customers, commercial partners, CMOs, and internal stakeholders • Supports day-to-day customer care operations for Telix Pharmaceuticals, US • Supports the commercial launch and ongoing operational needs of TLX101Px • Intake and triage of product-related requests • Coordination of internal escalations • Management of failure notifications from CMOs and radiopharmacies • Follow-up through case closure • Accurate documentation within ticketing and reporting systems • Works cross-functionally with Quality, Supply Chain, Logistics, Commercial, and other internal teams to support complaint handling, temperature reporting, non-conformances, production failures, and related issue resolution • Maintains strong knowledge of current and new products, services, systems, and policies to ensure high-quality customer and partner experience

• play a pivotal role in driving sales and maintaining strong relationships with clients within your assigned territory. • prospect new business opportunities. • manage existing accounts. • ensure the successful promotion and sales of our radiopharmaceutical products. • require a combination of strategic thinking, relationship-building skills, and a deep understanding of the radiopharmaceutical industry.

• Plays a pivotal role in ensuring the highest standards of product quality and compliance within our commercial operations • Responsible for overseeing and enhancing quality management systems • Driving continuous improvement initiatives • Overseeing contract manufacturing organizations • Collaborating with cross-functional teams focusing on TLX250-CDx and TLX101-CDx (18F-FET) moving through the commercialization space

• Define and set the operational strategy and long-term roadmap for the TMS Business Unit in alignment with enterprise priorities • Lead annual and multi-year strategic planning processes, ensuring clear priorities, investment focus, and measurable outcomes • Serve as a key advisor to BU and senior executive leadership, shaping business direction, growth strategies, and transformation agendas • Own evaluation and prioritization of strategic investments, including business development, partnerships, and M&A opportunities • Provide forward-looking, enterprise-level insights on performance, market dynamics, and competitive positioning • Own and lead the end-to-end strategic initiative portfolio, ensuring alignment with enterprise goals and delivery of measurable business value • Establish and enforce governance frameworks, decision rights, and operating cadence across initiatives • Drive prioritization, trade-off decisions, and resource allocation across competing initiatives at the BU level • Ensure clear accountability, execution rigor, and value realization across all strategic initiatives • Provide regular executive-level reporting and insights on portfolio performance, risks, and opportunities • Act as a trusted advisor and thought partner to executive leadership, shaping high-impact decisions • Lead executive forums and decision-making processes, ensuring alignment, clarity, and timely outcomes • Deliver insight-driven recommendations supported by rigorous analysis and financial evaluation • Influence decisions across enterprise stakeholders, driving alignment in complex and ambiguous situations • Lead cross-functional alignment at scale, partnering with leaders across Development, Sales, Finance, IT, and other functions • Drive enterprise-wide collaboration to ensure cohesive execution of strategy • Resolve complex interdependencies and organizational barriers, ensuring forward momentum on critical initiatives • Build strong, trusted relationships with senior leaders across the organization • Define and institutionalize best-in-class frameworks, tools, and operating models for strategy execution and portfolio management • Drive continuous improvement and transformation initiatives to enhance scalability, efficiency, and performance • Build and lead high-performing teams (directly or through influence), developing strategic, analytical, and execution capabilities • Establish a culture of accountability, performance, and continuous improvement across the Business Unit • Serve as a mentor and leader of leaders, elevating organizational capability

• Lead the planning, coordination, and execution of global regulatory submissions (e.g., INDs, CTAs, NDAs, BLAs, MAAs, and amendments), ensuring compliance with global regulatory requirements and timelines. • Provide operational oversight of eCTD submission activities, partnering with external publishing vendors and internal stakeholders to ensure high-quality, timely deliverables. • In partnership with the Senior Director of Regulatory Operations, play a key role in establishing internal publishing capabilities, including defining and leading implementation of publishing capability strategy • Ensure accurate maintenance of regulatory documentation, submission records, and data within regulatory information management and document management systems. • Oversee regulatory document management, tracking, and archival processes to ensure completeness, accuracy, and inspection readiness. • Serve as system administrator for regulatory systems (e.g., Veeva RIM) and act as the internal subject matter expert (SME), driving training, user adoption, and ongoing support in alignment with the defined system strategy and roadmap. • Ensure adherence to global submission standards, including eCTD structure, formatting, and publishing requirements. • Drive the development and continuous improvement of regulatory operations processes, tools, and best practices to enhance efficiency, quality, and consistency. • Lead, mentor, and develop a small team of regulatory operations staff, fostering a high-performing and collaborative team environment. • Oversee vendor relationships and outsourced publishing activities, ensuring performance, quality, and cost-effectiveness. • Partner with Regulatory Affairs leads to operationalize global submission strategies. • Collaborate cross-functionally with clinical, quality, and CMC teams to ensure alignment and execution of submission plans. • Monitor submission milestones and deliverables, proactively identifying risks and driving mitigation strategies to prevent delays. • Ensure ongoing compliance with global regulatory standards and organizational policies. • Maintain inspection readiness and support internal and external audits. • Ensure integrity, accuracy, and completeness of regulatory records and documentation. • Manage submission timelines, milestones, and deliverables across programs. • Lead risk assessment, escalation, and resolution to ensure successful execution of regulatory activities.

• Lead and oversee the strategic onboarding of new imaging sites, ensuring seamless integration of Telix radiopharmaceuticals into both commercial and clinical workflows. • Develop and implement best practices for imaging site optimization, including protocol standardization, scanner settings, and workflow efficiency improvements, ensuring high-quality imaging outcomes. • Oversee and execute key field activities for imaging sites in alignment with corporate strategy, ensuring optimal support for product launches and HCP education. • Build and maintain high-level collaboration with Territory Account Managers within their geography. • Contribute to the development and presentation of quarterly area business reviews. • Lead site engagement strategies, working closely with imaging centers, nuclear medicine specialists, and key stakeholders to ensure optimal patient access and product utilization. • Establish and manage a structured approach for education, developing training materials, presenting product information, and ensuring consistent knowledge dissemination to internal and external stakeholders. • Represent Telix at meetings and conferences, synthesizing insights that shape company strategy. • Oversee competitive intelligence gathering and market insights, ensuring internal teams have up-to-date knowledge of industry trends, emerging technologies, and competitive landscapes. • Act as a key liaison among cross-functional teams, ensuring alignment with cross-functional partnerships. Manage key projects and initiatives within the organization, ensuring efficient execution and measurable impact on Telix’s strategic goals. • Ensure compliance with pharmaceutical regulations, corporate policies, and ethical guidelines, proactively addressing any gaps in training or adherence.

• Progress a molecularly targeted radiation therapy through clinical trials up to and including Phase 2 • Create, implement, manage and execute the drug development plan • Lead a cross-functional team (including manufacturing, non-clinical, clinical, quality and regulatory) • Act as the primary point of contact for the program and maintain excellent communication • Oversight of a Project Manager to ensure application of project management best practice • Document and track the Program budget; ensure accurate and timely recording of costs • Assess product development risks and compile risk mitigation and scenario plans • Conduct regular reviews to monitor project progress, scope, timelines and budget • Represent the program team at internal and external meetings

• Responsible for the successful development of diagnostic-related products for the diagnosis of cancer • Creating, implementing, managing and executing the drug development plan • Leading a cross-functional team including manufacturing, non-clinical, clinical, quality and regulatory • Ensuring successful execution of all product development plans within project timelines and budget • Acting as the primary point of contact for the programs and ensuring good communication

• Manage the product lifecycle from end of Phase II through launch to maximize commercial outcomes • Drive action throughout the organization to get prostate cancer therapeutics to market, and maximize their impact • Translate business and portfolio strategy into product strategy • Lead cross-functional planning for market launch in each territory where the asset marketing application is filed, approved, and registered for commercialization • Provide input and support to develop and on-board key vendors to manage high priority commercial projects assigned by the global product leadership team • Support and challenge overall product COGs, global forecasts, and NPV analysis • Collect and manage market research, market access and competitive intelligence relevant to the asset product • Evaluate product functionality and drive future product direction • Develop the global cross-functional plan including forward looking budget commitments and business case for the total addressable market • Provide market insights to internal and external stakeholders on the product and therapy area • Own the monthly product roadmap, including the plan, organization and execution for all activities for the asset product • Drive coordination and delivery through all functional relationships – clinical, clinical operations, regulatory affairs, manufacturing, quality and medical affairs • Complete and smooth transition from Phase II team to Phase III team to launch • Support and drive all activities related to Phase III trials • Drive end to end project management activities including communication, timelines, budget management and reporting • Monitor and act on risks and opportunities, including escalating as appropriate