Clinical Supply Chain Specialist

Role: Clinical Supply Chain Specialist supporting Telix's clinical trial operations, focusing on the procurement, storage, and distribution of investigational and clinical supplies for oncology and rare disease programs. Responsibilities include managing inventory, developing supply strategies, maintaining vendor relationships, ensuring regulatory compliance (GMP, GDP), coordinating shipments, and optimizing supply chain efficiency. Requirements: Bachelor's in Supply Chain Management, Life Sciences, or related field; 3+ years in pharmaceutical or clinical trial supply chain management; strong knowledge of global regulatory standards; proficient in supply chain software; excellent organizational, communication, and problem-solving skills. Preferred: experience with early and late-stage drug development, clinical studies, and Regulatory Affairs; exposure to GxP environments. High-value specifics: focus on radiopharmaceuticals, late-stage clinical trials, and global logistics. Collaboration involves cross-regional teams, suppliers, and internal stakeholders. Work setup: hybrid/remote; no travel specified.