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- ...experience Technical Mastery: Deep knowledge of ICH-GCP and ISO14155 (for medical devices). Leadership: A track record of overseeing CRAs and managing multi-disciplinary, international teams. Communication: Excellent English skills (written and verbal) and the...Ofertas de empleo recomendadasTiempo completoContrato
- ...preparation for audit and required follow-up actions. May provide direct supervision, training and/or mentorship to more junior level CRAs. Performs training and sign off visits for junior CRA staff, as assigned. May be mentored and assigned lead tasks under supervision...Ofertas de empleo recomendadasInterinoContratoRemotoInicio inmediato
- ...and process study documentation from sites, check content and quality as well as completeness Interact with site personnel, CPCs, CRAs and PMs, for document corrections, clarification or resolution of any incomplete and/or incorrect documentation found during...Ofertas de empleo recomendadasRemoto
Consulting, Inc.
Madrid1 día atrás - ...functional teams to ensure timely and accurate data collection and reporting. Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct. Building and maintaining effective relationships with site personnel and...Ofertas de empleo recomendadasAutónomo
ICON
Madrid4 días atrás - ...conducted in accordance with ICH GCP guidelines, local and global regulatory requirements, and Novotech/Client SOPs. Responsibilities CRAs primary responsibility is to build relationships with Principal Investigators, study co-ordinators, pharmacists, and all relevant...Ofertas de empleo recomendadasRemotoHorario flexible
Life Sciences WA
Madrid2 días atrás - ...monitoring plans and tools, ensuring effective study oversight. Optimizing Performance: Train and mentor Clinical Research Associates (CRAs) to optimize their performance. Timely Study Start-Up & Enrollment: Drive enrollment and lead study start-up activities, adhering...Ofertas de empleo recomendadasAutónomo
ICON
Madrid4 días atrás - ...teams, to ensure a complete and accurate Trial Master File delivery. **Essential Functions** • Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master...Ofertas de empleo recomendadasInicio inmediato
IQVIA LLC
Madrid20 horas atrás - ...doing: • You will monitor multiple Phase I, II, III & IV clinical trial sites, across different therapeutic areas. Assist other CRAs with co-monitoring activities both remote and on-site. • You will utilise your customer service mindset with your sites focusing...Ofertas de empleo recomendadasAutónomoEmpleo permanenteRemoto
- ...and Categorization Tool (RACT). Reviews the study scope of work, budget and protocol content and ensures the clinical project team (CRAs/CeMs) is aware of the contractual obligations and parameters. Uses prior clinical experience, operational data, metrics and reports...Ofertas de empleo recomendadasTemporalContratoInicio inmediato
Syneos Health, Inc.
Madrid1 día atrás - ...investigators meetings and internal meetings related to study execution and operational excellence Interact with investigation sites and CRAs/CROs/vendors to ensure appropriate study setup and conduct Monitor site performance, review site visit reports and monitor...Ofertas de empleo recomendadasEmpleo permanenteContratoTrabajar en la oficinaRemoto
