[Remote] Clinical Supply Chain Specialist

Note: The job is a remote job and is open to candidates in USA. Telix Pharmaceuticals is seeking a Clinical Supply Chain Specialist to manage supply chain activities supporting clinical trial operations. The role coordinates sourcing, inventory, distribution, regulatory compliance, and stakeholder collaboration to ensure trial supplies are delivered efficiently and on time.

Responsibilities

• 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 any issues or discrepancies
• Arrange the shipment and delivery of clinical/commercial supplies to various sites, ensuring compliance with regulatory requirements and timelines
• Coordinate with logistics providers to ensure timely and secure transportation of materials
• Ensure that all supply chain activities comply with relevant regulatory guidelines and standards, including Good Manufacturing Practices (GMP) and Good Distribution Practices (GDP)
• Maintain accurate documentation and records for audit purposes
• Work closely with operational teams, project managers, and other stakeholders to understand study requirements and timelines
• Provide regular updates on supply chain status and address any issues or concerns
• Identify opportunities for process improvements and implement best practices to enhance supply chain efficiency and effectiveness
• Stay updated on industry trends and advancements in clinical trial supply chain management
• Other Supply Chain related items as assigned

Skills

• 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
• Strong communication skills, effective across all levels of the organization
• 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
• Demonstrate a dedication to continuous learning and professional growth, actively pursuing opportunities to enhance personal expertise and skill set
• Uphold integrity and exhibit a steadfast commitment to ethical conduct in all dealings with colleagues and stakeholders

Benefits

• Hybrid and remote work arrangements for employees located around the world
• Annual performance-based bonuses
• Equity-based incentive program
• Generous vacation
• Paid wellness days
• Support for learning and development
• An engaged and supportive group of colleagues

Company Overview

Company H1B Sponsorship