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Telix Pharmaceuticals is a dynamic, fast-growing radiopharmaceutical company with offices in Australia (HQ), Belgium, Japan, Switzerland, and the United States. Our mission is to deliver on the promise of precision medicine through targeted radiation. At our core, we exist to create products that seek to improve the quality of life for people living with cancer and rare diseases. You will be supporting the international roll-out of our approved prostate cancer imaging agent and helping us to advance our portfolio of late clinical-stage products that address significant unmet need in oncology and rare diseases.       See Yourself at Telix The Global Product Development Lead - Px will be responsible for the successful development of diagnostic-related products (up to and including Phase 3 clinical trials) for the diagnosis of cancer. The role will be responsible for creating, implementing, managing and executing the drug development plan. The successful delivery of the development plan will require leading a cross-functional team including manufacturing, non-clinical, clinical, quality and regulatory and a strong understanding of oncology drug development. This role is critical to the further development and successful delivery of Telix’s product portfolio by driving the current and future development of this newly acquired product. Key Accountabilities: Work as part of a cross-functional team to create product development and commercialisation plans of PSMA related products. Lead cross-functional teams to deliver the program and product development milestones up to the end of Phase 3 clinical evaluation. Successful execution of all product development plans through to the end of Phase 3 clinical evaluation within project timelines and budget. Oversight of Project Manager to ensure application of project management best practice, with the objective of progressing the Telix product portfolio through development within project timelines and budget. Act as the primary point of contact for the programs and ensure that good communication is maintained both internally and externally. Complete oversight of the successful delivery of product development plans and product approvals, more specifically: Maintenance of up-to-date documentation of product positioning and target product profile. Progress tracking of all activities against the development plan and notification of potential delays and/or other changes. Documentation and tracking of the Program budget; working with Finance and the project manager to ensure contracts and costs are recorded in an accurate and timely manner. Work with senior management to assess product development risks and compile risk mitigation and scenario plans Conducting regular reviews to ensure appropriate Program documentation is in place and to monitor project progress, scope, timelines and budget. Ensuring all Program Team members and the Executive are kept informed of project status, costs and risks. Supporting Project Managers in preparing periodic reports to internal stakeholders, including senior management, on the status and progress of the Program. Contribute to the definition and delivery of Corporate Objectives. Preparing timely and accurate reports for Management. Maintaining current awareness of Program-related scientific, clinical and commercial functional knowledge. Education and Experience: Bachelor’s degree required; Master’s or PhD strongly preferred 10+ years’ pharmaceutical/biotechnology industry experience including direct experience in oncology drug development required 5+ years’ project and budget management experience Non-clinical through Phase 4 experience an asset Diagnostics experience preferred An understanding of the regulatory environment in the US, EU and APAC Experience working as part of, and managing, a cross-functional team Line management experience strongly