
Supply and Logistics Specialist
Posted 4 days ago

Posted 4 days ago
This is a fully remote position, open to applicants in Argentina.
• Collaborate with Supply & Logistics Project Managers to create customized logistics concepts and solutions.
• Implement study-specific supply chain strategies, encompassing sourcing and distribution planning.
• Ensure visibility into study scope and monitor progress against timelines, budgets, and contractual obligations.
• Identify, manage, and communicate risks and modifications to stakeholders.
• Establish and uphold study-specific management tools and documentation.
• Optimize resource allocation for Full-Time Equivalent (FTE) coverage and project demands.
• Manage Pass-Through Costs with effective controls and transparent reporting.
• Develop clinical supply, sourcing, and distribution strategies in collaboration with cross-functional teams and stakeholders.
• Partner with third-party providers to negotiate scopes of work and enhance value.
• Plan and manage inventory in alignment with strategy, forecasts, and study needs.
• Create and sustain supply schedules based on feedback from the clinical team and study advancement.
• Communicate with depot partners to ensure smooth supply chain execution.
• Experience in the pharmaceutical, clinical research, or consulting sectors.
• Specialized knowledge in clinical logistics or related supply chain functions within the biopharmaceutical industry.
• Strong grasp of cross-functional activities and departmental interrelations.
• Extensive multinational work experience.
• In-depth understanding of GxP regulatory frameworks and ICH GCP guidelines.
• Proficient in English.
• Bachelor’s or Master’s degree in Biology, Pharmacy, International Trade, Business Administration, Logistics, or a related health discipline.
• Equivalent professional experience will be considered.
• PharmD or a similar advanced qualification is preferred.
• Demonstrated consultative selling and negotiation skills.
• Strong to excellent operational understanding.
• Proficient in MS Office Suite and willing to learn new tools.
• Growth: Work on diverse, complex projects that challenge and enhance your skills.
• Culture: Join a collaborative, innovative team that values excellence and continuous improvement.
• Global Reach: Interact with multinational teams and gain insights into international clinical trial operations.
• Compliance & Quality: Operate in a highly regulated environment where quality and compliance are critical.
• Career Development: Opportunities to mentor, lead, and advance within a growing organization.
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