Remote Senior Manager, Clinical Supply Chain

Summary

Join Telix Pharmaceuticals as a Senior Manager, Clinical Supply Chain to oversee and manage the end-to-end supply chain activities related to clinical trials and the distribution of radiopharmaceutical products.

Requirements

• Bachelor’s degree in relevant scientific or business discipline required
• 8+ years’ experience in clinical supply chain management within the pharmaceutical, biotechnology, or radiopharmaceutical industry, with increasing levels of responsibility required
• Strong understanding of clinical trial supply chain processes, including demand forecasting, planning, sourcing, and distribution
• Excellent knowledge of relevant regulations, guidelines, and standards governing clinical supply chain operations, such as Good Manufacturing Practice (GMP), Good Clinical Practice (GCP) and Good Distribution Practice (GDP)
• Proficiency in utilizing supply chain management software systems and tools
• Exceptional problem-solving and analytical skills, with the ability to make sound decisions in complex and time-sensitive situations
• Strong communication and interpersonal skills, with the ability to collaborate effectively across functions and regions and influence key stakeholders
• Detail-oriented mindset, with a focus on accuracy, quality, and compliance

Responsibilities

• Develop and implement strategic plans and operational strategies for the clinical supply chain, ensuring alignment with the company’s overall objectives and goals
• Oversee all aspects of clinical supply chain management, including demand forecasting, planning, sourcing, procurement, inventory management, packaging, labeling, and distribution
• Collaborate with cross-functional teams to establish and maintain effective relations with clinical sites, CMOs, and third-party logistics providers, ensuring the timely and accurate delivery of clinical supplies
• Partner with Clinical Operations and Manufacturing teams to define and manage clinical trial supply strategies, including drug forecasting, demand planning, and comparator sourcing
• Coordinate and manage investigational product labeling, packaging, and distribution activities, ensuring compliance with regulatory guidelines and internal quality standards
• Collaborate with Regulatory and Quality teams to ensure compliance with all relevant regulations, guidelines, and standards governing clinical supply chain operations
• Proactively identify and mitigate potential supply chain risks and develop contingency plans to address any potential disruptions to the clinical supply chain
• Independently responsible for conceptualization, development, and implementation of clinical supply plans, based on clinical study protocol and clinical development plans
• Develops program models, contributes to the study specifications for IWRS studies, and provides medication management for highly complex studies using IWRS and predictive tools
• Track and analyze key supply chain metrics and performance indicators, providing regular reports and recommendations for process improvements and cost optimization

Benefits

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