Clinical Supply Chain Specialist

Posted 1 day ago

This is a fully remote position, open to applicants in United States.

📋 Description

• Oversee the acquisition, storage, and distribution of clinical and commercial supplies, which includes investigational products, lab kits, and other materials.

• Manage inventory levels effectively to avoid shortages or excess stock.

• Create and execute supply chain strategies aimed at enhancing efficiency and cost-effectiveness.

• Build and sustain relationships with suppliers and vendors.

• Evaluate vendor performance and resolve any issues or discrepancies.

• Organize the shipment and delivery of clinical and commercial supplies to various locations, ensuring adherence to regulatory requirements and timelines.

• Collaborate with logistics providers to ensure timely and secure transportation of materials.

• Ensure compliance with regulatory guidelines and standards, including GMP and GDP.

• Maintain precise documentation and records for audit purposes.

• Work alongside operational teams, project managers, and stakeholders to align on study requirements and timelines.

• Provide consistent updates on supply chain status and address any issues or concerns.

• Identify areas for process improvement and implement best practices.

• Keep abreast of industry trends and advancements in clinical trial supply chain management.

• Perform additional supply chain-related tasks as assigned.


⛳️ Requirements

• A Bachelor’s degree in Supply Chain Management, Logistics, Life Sciences, or a related field is required.

• A minimum of 3 years of experience in supply chain management, ideally within the pharmaceutical or clinical trial sectors, is required.

• Solid understanding of regulatory requirements and industry standards pertaining to global supply chains.

• Exceptional organizational and time management abilities, capable of handling multiple tasks concurrently.

• Strong communication and interpersonal skills, with the capability to collaborate effectively with cross-functional teams.

• Proficient in supply chain management software and tools.

• Keen attention to detail and strong problem-solving skills.

• Advanced understanding of both early and late-stage drug development processes, encompassing clinical and non-clinical requirements.

• Familiarity with clinical studies and regulatory affairs.

• Strong ability to collaborate effectively with teams across different regions.

• Commitment to continuous learning and professional development.

• Integrity and dedication to ethical conduct.


🏝️ Benefits

• Annual performance-based bonuses.

• Equity-based incentive program.

• Generous vacation policy.

• Paid wellness days.

• Support for learning and professional development.

• Competitive salary packages.

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