AbbVie seeks a Clinical Monitoring professional to oversee site activities, ensure protocol adherence, and manage regulatory compliance across Phase 1–4 trials. Based remotely from Madrid, you will coordinate monitoring visits, data quality, and safety reporting with study teams.
Adecuado candidates hold a health-related degree (Master’s in Clinical Trials preferred) and have 1 year of clinically-related experience, including site monitoring exposure. A strong grasp of ICH/GCP is essential.
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📌 Remote Clinical Research Associate I — Madrid
🏢 AbbVie
📍 Madrid