Clinical Study Operations Specialist
Link-Worldwide
Responsabilidades
- Preparación y organización de los estudios clínicos del departamento.
- Participación en la ejecución y reporte de estudios clínicos.
- Gestionar información y redactar documentos técnicos.
- Mantenimiento y animación del sistema de calidad del departamento.
- Manejo y control de los CRO’s (Organizaciones de Investigación por Contrato) para estudios clínicos.
- Búsqueda y resguardo de información técnica.
Vacante publicada el 3 días atrás
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