Clinical Supply Chain Specialist

🕒 September 29

🇺🇸 United States – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🔗 Supply Chain

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Telix Pharmaceuticals Limited

WebsiteLinkedInAll Job Openings

501 - 1000 employees

Founded 2015

🏥 Healthcare

💼 Consulting

🧬 Biotechnology

Healthcare • Consulting • Biotechnology

Telix Pharmaceuticals Limited is a commercial-stage biopharmaceutical company dedicated to transforming the way cancer and rare diseases are diagnosed and treated. Focusing on the development and commercialization of theranostic radiopharmaceuticals, Telix utilizes targeted radiation to enhance treatment decision-making and deliver personalized therapy. With an extensive pipeline addressing areas such as prostate and kidney cancer, neuro-oncology, and musculoskeletal cancers, Telix has garnered global regulatory approvals for its lead imaging agent, Illuccix®, and is actively conducting numerous clinical trials worldwide.

📋 Description

• Coordinate the procurement, storage, and distribution of clinical/commercial supplies, including investigational products, lab kits, and other materials • Maintain inventory levels and manage stock to prevent shortages or overages • Develop and implement supply chain strategies to optimize efficiency and cost-effectiveness • Establish and maintain relationships with suppliers and vendors • Monitor vendor performance and address issues or discrepancies • Arrange shipment and delivery of clinical/commercial supplies to various sites while ensuring regulatory compliance and timelines • Coordinate with logistics providers for timely and secure transportation of materials • Ensure compliance with regulatory guidelines and standards, including GMP and GDP • Maintain accurate documentation and records for audits • Collaborate with operational teams, project managers, and stakeholders on study requirements and timelines • Provide regular supply chain status updates and address issues or concerns • Identify process improvements and implement best practices • Stay updated on industry trends and advancements in clinical trial supply chain management • Perform other supply chain-related duties as assigned

🎯 Requirements

• Bachelor’s degree in Supply Chain Management, Logistics, Life Sciences, or a related field required • 3+ years of experience in supply chain management, preferably in the pharmaceutical or clinical trial industry required • Strong knowledge of regulatory requirements and industry standards related to global supply chain • Excellent organizational and time management skills with the ability to manage multiple tasks simultaneously • Strong communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams • Proficiency in supply chain management software and tools • Attention to detail and problem-solving abilities • Proficient understanding of both early and late-stage drug development processes, including clinical and non-clinical requirements, at an advanced level • Exposure to Clinical studies and Regulatory Affairs • Strong ability to collaborate effectively with teams across various regions • Dedication to continuous learning and professional growth • Integrity and commitment to ethical conduct

🏖️ Benefits

• Annual performance-based bonuses • Equity-based incentive program • Generous vacation • Paid wellness days • Support for learning and development • Competitive salaries