Clinical Research Associate

hace 3 semanas


Madrid, España Antal International Network A tiempo completo

Monitorización del proceso de investigación clínica, incluyendo la gestión de suministros y la coordinación.Supervisar la recopilación y documentación de datos y la introducción de datos en sistemas de bases de datos.Especificar los objetivos del ensayo y presentar los protocolos al comité.Proteger la confidencialidad de los sujetos.Preparación de informes posteriores al ensayo.Experiencia previa en Industria Farmacéutica y/o ensayos clínicos.Buenos conocimientos informáticos.Inglés avanzado.Capacidad de organización del tiempo y resolución de problemas.#J-18808-Ljbffr



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