ICON plc is seeking a CRA II for a hybrid role in Mexico City (CDMX).
You will design and analyse clinical trials, monitor sites, and ensure data integrity and patient safety across studies.The role requires a minimum of 2 years as a Clinical Research Associate, a strong understanding of ICH-GCP, and the ability to travel up to 60%.
You will collaborate with investigators and study teams to drive quality and compliance.
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📌 Senior Cra Ii: Drive Trials With Travel‐Ready Flexibility (Xico)
🏢 Icon Clinical Research
📍 Xico
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