Clinical Supply Chain Site Lead

🕒 6 days ago

🇺🇸 United States – Remote

⏰ Full Time

🟠 Senior

🔗 Supply Chain

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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

• Serve as the primary clinical supply chain contact and escalation lead for late-stage and Phase III clinical trial sites • Build site relationships and ensure issues are documented, communicated, and followed through to closure • Manage site-level communications on investigational product deliveries, shipment status, dose scheduling, product receipt, and supply continuity • Coordinate resolution with Quality, Clinical Operations, Logistics, Manufacturing, and external partners for temperature excursions, shipment deviations, product complaints, and other events • Assess root causes, implement corrective actions, and track distribution disruptions and CAPAs to closure • Collect, trend, and assess site feedback, satisfaction concerns, and recurring operational issues • Present site feedback, operational metrics, escalations, risks, mitigation plans, and lessons learned to study teams and leadership • Identify and implement process improvements to improve supply reliability, service levels, cost-effectiveness, and site satisfaction • Contribute to clinical supply chain strategy • Ensure compliance with regulations, GMP, GDP, company policies, and study-specific requirements • Maintain accurate documentation, issue logs, and audit-ready files

🎯 Requirements

• Bachelor’s degree in Supply Chain Management, Business, Life Sciences, or a related field required; equivalent combination of education and relevant experience will be considered • Minimum of 5 years of experience in pharmaceutical, biotechnology, clinical research, or healthcare supply chain operations • Minimum of 3 years of experience managing clinical supply chain activities required, preferably supporting global clinical trials and late-stage development programs • Demonstrated knowledge of clinical supply chain processes, including forecasting, inventory management, manufacturing, distribution, and site support • Strong understanding of applicable regulatory requirements, Good Manufacturing Practices (GMP), Good Distribution Practices (GDP), and global supply chain compliance standards • Ability to manage multiple priorities in a fast-paced environment while maintaining accuracy and attention to detail • Organizational, project management, and problem-solving skills with the ability to identify risks and implement solutions • Strong verbal and written communication skills for engaging clinical sites, suppliers, and cross-functional stakeholders • Experience leading cross-functional issue resolution efforts and managing escalations • Proficiency with supply chain planning systems, ERP platforms, clinical trial management tools, Smartsheet, and Microsoft Office • Ability to analyze data, identify trends, and develop actionable recommendations • Experience working with global suppliers, logistics providers, CMOs, and clinical trial sites preferred

🏖️ Benefits

• Competitive salaries • Annual performance-based bonuses • Equity-based incentive program • Generous vacation • Paid wellness days • Support for learning and development • Hybrid and remote work arrangements are available within Telix • Equal opportunity employment

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