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Madrid, Madrid, España Worldwide Clinical Trials A tiempo completo{"title": "Clinical Research Associate - Site Management", "content": "Role OverviewAs a Clinical Research Associate - Site Management, you will play a vital role in ensuring the quality and excellence of our clinical research programs. You will be responsible for conducting site qualifications, initiation, interim monitoring, site management, and study...
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Clinical Research Associate
hace 4 meses
Actuar como intermediario entre el promotor de una investigación, el investigador y las instituciones
Buena relación con los centros de investigación para garantizar que cumplen con los tiempos establecidos.
Colaborar en la preparación y asistencia a reunión de investigadores.
Planificación y realización de todo tipo de visitas (viabilidad, selección, monitorización y cierre) de acuerdo con el plan monitorización.
Gestión del envío de los materiales del proyecto.
Detectar y asegurar el correcto manejo de los acontecimientos adversos y reacciones adversas ocurridas en pacientes dentro de un proyecto de investigación.
Garantizar la integridad de los datos y mantener actualizados todos los registros, documentos y material de los proyectos en investigación asignados.
Requisitos:
Al menos 1 AÑO como CRA en la gestión de centros, incluyendo visitas de monitorización en una CRO o en la industria farmacéutica.
Master en investigación clínica o experiência equivalente.
Gran capacidad de trabajo en equipo
Gran capacidad de comunicación e interacción con otros equipos.
Conocimiento de las guías ICH-GCP y legislación local e internacional en materia de investigación clínica.
Nível alto de inglés hablado y escrito (valorable Portugués).
CONDICIONES
INCORPORACIÓN:
Inmediata.
REMUNERACIÓN:
Según experiência