Logistics coordinator | ENG | Zaventem

ADECCO; Sint-Stevens-Woluwe; On-site; EUR 38,000 - 55,000; Full time

Job summary

Zaventem Clinical Research is seeking a Logistics Coordinator to manage end-to-end supply chain activities for clinical studies in the Brussels area. The role covers ordering, receiving, storage, shipping and delivery of drugs, devices, and lab supplies, plus accounting for returns and regulatory compliance.

Responsibilities include local purchasing, distribution to clinical sites, and ensuring documentation and destruction of returns where applicable, with a focus on efficiency and accuracy in

Responsibilities

• You are responsible and accountable for the ordering, receiving, processing, storage, shipment, and delivery of drug products, medical devices, and lab supplies.
• You manage returned materials from clinical sites, including drug accountability, reconciliation, and destruction processes.
• You ensure accurate administration and documentation of all supply chain and logistics activities for assigned studies.
• You perform local purchasing activities as requested.
• You coordinate logistics activities for studies of low to moderate complexity.
• You ensure compliance with relevant procedures, quality standards, and regulatory requirements.
• You support the timely and efficient distribution of study materials to clinical sites.

Job description

We are looking for a logistics coordinator for a large medical company specialized in clinical research in Zaventem.

Your tasks:

You are responsible and accountable for the ordering, receiving, processing, storage, shipment, and delivery of drug products, medical devices, and lab supplies.

You manage returned materials from clinical sites, including drug accountability, reconciliation, and destruction processes.

You ensure accurate administration and documentation of all supply chain and logistics activities for assigned studies.

You perform local purchasing activities as requested.

You coordinate logistics activities for studies of low to moderate complexity.

You ensure compliance with relevant procedures, quality standards, and regulatory requirements.

You support the timely and efficient distribution of study materials to clinical sites.