PPD are looking for experienced Clinical Research Associates at various levels who are interested to join our team of Home Based CRA's in Barcelona or office based in Madrid. Due to increasing client needs within Spain we are continuing to network wi
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
Develops/maintains study documents and utilizes company systems to manage clinical/biomedical studies. Provides administrative support to project team members in clinical operations and project management. Works with the project team to ensure that p
Your mission is to provide customers the best clinical support: This position is mainly responsible for clinical communication and support to external and internal customers. The process includes interaction and communication with private-practicing
Empresa: PPD Europe. País: España. Provincia: Madrid. Sector: Legal. Fecha: 15 de octubre Requisitos: Ideally a legal degree, and up to 2 years' experience in the privacy field. Project management skil
Research es una función estratégica en CoStar Group. El equipo de Research es responsable del estudio, análisis y la actualización de la información de edificios de oficinas, locales comerciales, naves y otros inmuebles de inversión, proporcion
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
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