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Remote CRA I – Site Monitoring & Compliance

Descripción del empleo

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 ideal 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.

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Información extra

Status
Activa
Estudios requeridos
E.S.O
Localización
Madrid
Tipo de contrato
Tiempo completo
Publicado el
04-10-2026
Carnet de conducir
No
Vehículo
No
Carta de motivación
No

Madrid | Tiempo completo | E.S.O

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