
1001 - 5000 employees
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
Biotechnology • Pharmaceuticals • Healthcare Insurance
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.
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1001 - 5000 employees
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
Biotechnology • Pharmaceuticals • Healthcare Insurance
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.
• Plan, implement and monitor study supply strategy overall supply chain strategy in order to maximize efficiency and productivity • 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 efficiency throughout the supply chain while ensuring quality and safety; implements subsequent changes to processes. • Collaborate with DLS Leadership to define and implement key supply chain KPIs at study and functional levels • Identify process bottleneck and implement solutions in a timely manner • Performs other related duties as assigned.
• Bachelor’s Degree in Life Science, Clinical Supply Chain Management, Finance, or a similar relevant field • Clinical research setting experience required (1 year minimum) • Previous experience in the supply chain operations required (1-2 years) • Hands-on experience with supply chain functionality in an IRT/RTSM system is a plus • Strong planning skills • Logical and systematic approach to work • Good time management, with the ability to work under pressure, maintain accuracy and keep to deadlines • Excellent relationship management skills, with the ability to work collaboratively with internal and external teams • Negotiation and influencing skills • Business management and analytical skills • IT literacy, skills in Excel and the ability to handle electronic data • Understanding of risk management in the context of the supply chain.
• Health insurance • Retirement plans • Professional development opportunities
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