Clinical Supply Chain Specialist

Telix Pharmaceuticals Limited

. Coordinate the procurement, storage, and distribution of clinical/commercial supplies, including investigational products, lab kits, and other materials .

Posted 9/29/2026full-timeRemote • United StatesMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in supply chain management within the pharmaceutical and clinical trial sectors, focusing on regulatory compliance, inventory management, and vendor relations. Proficient in optimizing supply chain strategies and maintaining accurate documentation for audits.

Highest-signal resume keywords

Supply Chain ManagementRegulatory ComplianceInventory ManagementVendor Relationship ManagementClinical Trial Supply Chain

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Supply Chain ManagementInventory ManagementRegulatory ComplianceClinical Trial ProcessesProcess ImprovementLogistics CoordinationDocumentation ManagementProblem-SolvingGMP KnowledgeGDP Knowledge

Soft Skills

Organizational SkillsTime ManagementCommunication SkillsInterpersonal SkillsCollaboration

Tools & Technologies

Supply Chain Management Software

Industry Keywords

Pharmaceutical IndustryClinical TrialsRegulatory AffairsGlobal Supply ChainLife Sciences

About the role

Key responsibilities & impact

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

What you’ll need

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

Comp & perks

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