AbbVie is seeking a Clinical Research Monitor to oversee activities at investigative sites for Phase 1-4 trials, ensuring protocol adherence and regulatory compliance. The role emphasizes data integrity, safety reporting, and readiness for regulatory inspections.
The adecuado candidate has at least 1 year of clinically-related experience, preferably 6 months in monitoring or as a Study Coordinator, and a health-related qualification; Clinical Trials Master's degree is preferred.
📌 Remote CRA I – Site Monitoring & Compliance (Madrid)
🏢 Smartrecruiters
📍 Madrid
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