30 sep
|
Tigermed
|
Murcia
Tigermed is seeking a Clinical Research Associate to oversee study site selection, initiation, monitoring, and safety reporting in compliance with protocol and ICH-GCP guidelines. The role includes coordinating materials, training site staff, and ensuring timely documentation throughout the study lifecycle.
The idóneo candidate will have a Bachelor degree or higher in a medical field, at least 8 years of CRA experience, solid GCP knowledge, and strong MS Office skills.
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📌 Contract CRA: Start-Up & Monitoring for Clinical Trials (Murcia)
🏢 Tigermed
📍 Murcia