Salario promedio: €1702 /mensual
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- ...role to ensure sustainable trial start-up at Site. The Study Start-Up CRA is accountable for site selections as well as study-specific start-up activities and deliverables of assigned sites for Phase I-IV trials in the country in accordance with monitoring procedures and...Ofertas de empleo recomendadas
- ...trial start‑up at site. Responsible for site selections, study‑specific start‑up activities and deliverables of assigned sites for Phase I‑IV trials in the country in accordance with monitoring procedures and processes following ICH/GCP, local regulations and SOPs. Job...Ofertas de empleo recomendadas
- ...Associate in Madrid, Spain. The candidate will be responsible for site management and ensuring timely trial start-up activities for Phase I-IV studies. Key responsibilities include site selection, relationship management, and collaboration with various stakeholders....Ofertas de empleo recomendadas
- Syneos Health, Inc. is looking for a Senior Clinical Research Associate I based in Barcelona or Madrid to manage clinical trials in oncology. This role requires strong experience in site qualification and monitoring, ensuring compliance with regulations and documentation...Ofertas de empleo recomendadas
- Syneos Health is looking for a Sr. CRA I to join their team in Spain. This role involves site management from qualification to close-out for oncology clinical trials across the country. The ideal candidate will have a Bachelor’s degree or RN, strong experience in oncology...Ofertas de empleo recomendadasRemoto
- Syneos Health, Inc. is seeking a Senior Clinical Research Associate (SrCRA I) to manage clinical trial sites in Madrid or Barcelona. This role requires a strong background in oncology clinical trials and entails performing site qualifications, initiations, and compliance...Ofertas de empleo recomendadasRemotoTrabajo híbrido
- ...CRA II - Sr CRA I. Spain. Sponsor dedicated. Experience in dermatology, CNS and cardiology studies. Updated: Yesterday Location: Madrid, Spain Job ID: 25108540 Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate...Ofertas de empleo recomendadasInterinoContratoRemoto
- Syneos Health, Inc. is seeking a Study Start-Up CRA in Barcelona, Spain. The role focuses on relationship management to ensure sustainable trial start-up across assigned sites. Responsibilities include conducting site selection visits, managing study start-up activities...Ofertas de empleo recomendadasContrato
- Syneos Health, Inc. is seeking a Study Start-Up CRA in Madrid, Spain. The role involves managing site selection and ensuring timely progression of trials through effective collaboration with various stakeholders. Responsibilities include preparing necessary documents, negotiating...Ofertas de empleo recomendadas
- ...in Madrid, Spain. This role involves managing relationships with clinical trial sites, ensuring timely start-up activities for Phase I-IV trials. Responsibilities include conducting site selection visits, coordinating with Study Start-Up Teams, and ensuring compliance...Ofertas de empleo recomendadas
- ...met. Must be able to quickly adapt, with the oversight of the Lead CRA, to changing priorities to achieve goals / targets. May act as... ...required follow‑up actions. For Real World Late Phase, the CRA I will use the business card title of Site Management Associate I. Additional...Ofertas de empleo recomendadasInterinoContratoRemotoInicio inmediato
- ...met. Must be able to quickly adapt, with the oversight of the Lead CRA, to changing priorities to achieve goals/targets. May act as... ...required follow‑up actions. For Real World Late Phase, the CRA I will use the business card title of Site Management Associate I. Additional...Ofertas de empleo recomendadasInterinoContratoRemotoInicio inmediato
- Syneos Health, Inc. is seeking a CRA II - Sr CRA I based in Madrid. This role involves managing site-level activities in clinical studies, ensuring compliance with regulations while monitoring data integrity. Candidates should have a Bachelor’s degree and 2-3 years of CRA...Ofertas de empleo recomendadas
- Syneos Health, Inc. is looking for a Study Start‑Up CRA based in Madrid, Spain. The role involves managing site relationships and ensuring timely trial start-ups for Phase I‑IV studies. Key responsibilities include site selection, preparation of essential documents, and...Ofertas de empleo recomendadas
- ...a Catalunya cerca personal tècnic amb experiència en laboratori bioquímic per donar suport a l'equip en anàlisis, gestió d'inventari i manteniment d'equips. Les responsabilitats inclouen la gestió de compres, residus i cura d'animals d'experimentació. Aquesta és una oportunitat...Ofertas de empleo recomendadas
- ...requirements and all applicable laws. Key Requirements Bachelor degree in life-science Min 1 year monitoring experience as CRA within a CRO, Pharma, Biotech Experience in commercial studies Experience with site initiation, site close out Experience in...
- ...full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a CRA sponsor dedicated home based in Andalusia. Job Overview Monitoring clinical studies in phases II-III Assuring adherence to Good...Desde casa
- ...full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a CRA / Clinical Research Associate Regional Monitoring in Barcelona Job Overview Monitoring clinical studies in phases II-III Assuring...
- ...effective working relationships with coworkers, managers, and clients. • Awareness of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training. •...Inicio inmediato
- ...innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements...Autónomo
- A biopharmaceutical services company is seeking a Clinical Research Associate (CRA) to oversee site management and ensure compliance with clinical trials. As the primary contact at clinical sites, you will conduct visits, build relationships, and monitor data quality. The...
- A leading healthcare intelligence organization is seeking a Clinical Research Associate II to contribute to clinical trials by ensuring protocol compliance and data integrity. Ideal candidates will need a Bachelor's degree in a scientific field and at least 2 years of experience...
- ...Clinical Practices, and supervise study conduct. The ideal candidate should have a Bachelor degree in life-science, at least 1 year of CRA experience, and fluency in English and Spanish. Excellent communication skills and a full clean driver's license are required. #J-...
- A global CRO in Barcelona is seeking a Clinical Research Associate (CRA) for monitoring clinical studies in phases II-III. This role requires a Bachelor degree in life-science, at least one year of monitoring experience, and fluency in both English and Spanish. The ideal...
- Antares Consulting SA en Barcelona busca un/a Clinical Research Associate (CRA) para supervisar ensayos clínicos, garantizando el cumplimiento de protocolos y regulaciones. Se requiere una Licenciatura en Ciencias de la Salud, un Máster en Gestión de Ensayos Clínicos, y...Horario flexible
- ...and manage required documentation. You will manage procedures and guidelines from different sponsors and/or monitoring environments (i.e., FSO, FSP, Government, etc.). Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with...Trabajo remotoTrabajar en la oficinaDesde casaTurno de noche
- As a CRA sponsor dedicated, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare... ...What you will be doing: • You will monitor multiple Phase I, II, III & IV clinical trial sites, across different therapeutic...AutónomoEmpleo permanenteRemoto
- A global biopharmaceutical solutions company in Barcelona is seeking a Clinical Research Associate to oversee clinical research studies and ensure compliance with regulatory requirements and protocols. Responsibilities include conducting site management, verifying informed...Remoto
CSO: Data Manager/CRA in house MFAR, S.L. calendar_month hace 16 horas place Barcelona, Madrid,[...]
Overview Tipo de contrato: Indefinido, con 6 meses de prueba. Profesional de la salud con formación en el área de Ensayos Clínicos para la gestión de bases de datos de ensayos clínicos y EPAs (data specialist). Responsibilities Monitorización remota de ensayos...IndefinidoTrabajo de veranoTrabajar en la oficinaRemotoJornada intensiva- Una empresa del sector salud busca un especialista en ensayos clínicos con al menos 2 años de experiencia. La persona seleccionada será responsable de la monitorización remota de ensayos clínicos y la revisión de datos. Se valorará la formación en ensayos clínicos y el ...IndefinidoTrabajo de veranoRemotoJornada intensivaHorario flexible
