Global Clinical Lead

Role: Global Clinical Lead responsible for designing, leading, and implementing clinical development strategies for Telix's therapeutic assets in oncology and rare diseases, with a focus on radiopharmaceuticals. Responsibilities: oversee clinical trial design from concept to protocol, collaborate with cross-functional teams including Regulatory, Medical Affairs, and Clinical Operations, and manage the creation of clinical documentation and regulatory submissions. Lead data review to ensure integrity and quality, contribute to regulatory documents, and engage with external stakeholders such as KOLs, regulators, and partners. Qualifications: MD/MBBS, 5+ years in industry clinical development, with proven experience in oncology or nuclear medicine, and early-stage trial expertise. Strong regulatory knowledge (FDA, EMA), leadership skills, and strategic/scientific acumen are essential. HighValue: oncology/radiopharmaceutical therapy, clinical stage (late-stage), global regulatory engagement, cross-functional leadership, and experience in clinical trial design and data interpretation. WorkSetup: hybrid/remote, with global collaboration.