Clinical Supply Specialist – LATAM/Europe

🔥 0 minutes ago

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟢 Junior

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Worldwide Clinical Trials

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Worldwide Clinical Trials is a global contract research organization (CRO) that provides comprehensive clinical trial services. They specialize in supporting studies across diverse therapeutic areas such as oncology, cardiology, and rare diseases. With over 30 years of experience, Worldwide Clinical Trials emphasizes personalized support and customized solutions throughout the entire lifecycle of drug development. Their services include clinical monitoring, data management, patient recruitment, and regulatory consulting, ensuring precision and tailored attention for each clinical trial.

📋 Description

• Plan, implement, monitor, and improve study supply strategy and overall supply chain strategy • Optimize supply levels to ensure continuity while minimizing carrying costs • Control manufacturing and delivery processes • Collaborate with Project Management, Vendor Management, and DLS Leadership • Develop and maintain detailed inventories of study drug • Develop procedures to increase supply chain efficiency while ensuring quality and safety • Implement subsequent process changes • Define and implement key supply chain KPIs at study and functional levels with DLS Leadership • Identify process bottlenecks and implement timely solutions • Perform other related duties as assigned

🎯 Requirements

• Strong planning skills • Logical and systematic approach to work • Good time management, ability to work under pressure, maintain accuracy and meet deadlines • Ability to solve problems, make decisions, and think strategically and laterally • Excellent relationship management skills and ability to collaborate with internal and external teams • Negotiation and influencing skills • Business management and analytical skills • IT literacy and Excel skills; ability to handle electronic data • Understanding of supply chain risk management • Bachelor’s Degree in Life Science, Clinical Supply Chain Management, or a similar relevant field • Clinical research setting experience required (1 year minimum) • Clinical supply chain operations experience required (1 year minimum) • Hands-on experience with supply chain functionality in an IRT system (preferred) • Sense of ownership, critical thinking, detail-oriented and problem-solving skills • Excellent communication skills

🏖️ Benefits

• Equal employment opportunities regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law