Tigermed in Spain seeks a Senior CRA to oversee site selection, initiation (SIV) and ongoing monitoring across multiple studies, ensuring adherence to protocol and ICH-GCP. You will provide site staff training on study requirements, coordinate safety reporting and SAE timelines, and manage study materials, EC submissions, and trial master file updates.
Extensive experience in clinical operations (8+ years) and solid MS Word/Excel/PPT skills are required; knowledge of study tools and budget
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📌 Senior Clinical Research Associate - Site Monitoring (Lugo)
🏢 Tigermed
📍 Lugo