As a Regulatory Affairs Associate at PRA you will work on the preparation and review of regulatory submissions for both internal customers and external clients. Responsibilities will include: * Preparation of clinical trial submissions to support
Working as an integral part of the PRA full-service study team and for a varied mix of sponsors, the Clinical Research Associate is ultimately responsible for the successful management of investigator sites throughout the site lifecycle, whilst worki
Working fully outsourced to our global pharmaceutical client, the Clinical Research Associate is ultimately responsible for the successful management of investigator sites throughout the site life-cycle, whilst working in accordance with ICH-GCP guid
Working as an integral part of the PRA full-service study team and for a varied mix of sponsors, the Clinical Research Associate is ultimately responsible for the successful management of investigator sites throughout the site lifecycle, whilst worki
Working as an integral part of the PRA full-service study team and for a varied mix of sponsors, the Clinical Research Associate is ultimately responsible for the successful management of investigator sites throughout the site lifecycle, whilst worki
Working as an integral part of the PRA full-service study team and for a varied mix of sponsors, the Clinical Research Associate is ultimately responsible for the successful management of investigator sites throughout the site lifecycle, whilst worki
The Regulatory Affairs Associate (RAA) is responsible for preparing, submitting and following up on initial and amended Ministry of Health (MoH), Central Independent Ethics Committee (IEC), and any other central submissions required in the country(s)
Seleccionamos para cliente final un consultor con experiencia en implantación y manejo de Veeva CRM. Su misión consistirá en dar soporte a los usuarios en cuanto al uso y manejo de la herramienta, consiguiendo que obtengan el máximo partido de la
Empresa: ADECCO. País: España. Provincia: Madrid. Sector: Ingeniería y producción. Fecha: 09 de octubre Requisitos: Se requiere Licenciatura / Ingeniería Superior; Experiencia no requerida. - Experie
Gestión de todas las actividades regulatorias relacionadas con el ciclo de vida de los productos de la compañía. Control de las distintas fases de evaluación de la documentación, coordinando las respuestas a posibles declaraciones y ajuste del c
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