ICON is a integral healthcare intelligence and clinical research organisation focused on bringing new medicines to patients faster. As a Regulatory Technician, you will work with the Clinical Trials Information System (CTIS) and support submissions and related documents, coordinating resources for submissions and ensuring compliance across projects.
You will proactively identify risks via CTIS helpdesks, manage study-level CTIS access, and perform data entry and document uploads while maintaining
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📌 Ctis regulatory technician - submissions & data management (Cataluña)
🏢 Icon Clinical Research
📍 Cataluña
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