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Cra Spain- da El Paso de Cra Ii a Senior-single
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Madrid, España NonStop Consulting A tiempo completoSi eres uno de esos CRA II que quieres dar el salto a Senior CRA y te gustaria trabajar sponsor dedicated este es tu post!! Uno de nuestros clientes tiene varias vacantes como Senior CRA sponsor dedicated con distintos sponsors para CRAs con al menos 3 años de experiência monitorizando ensayos clinicos. Ademas, algunos sponsor no trabajan con oncologia,...
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Cra Ii y Senior- Madrid-promocion en Base a
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Madrid, España NonStop Consulting A tiempo completo¿Que te pareceria un puesto en el que la promocion depende de ti? En el que se te marcan unos objetivos en base al puesto que quieres y te entrenan para ello? Y como te quedas si te digo que ademas tienen un limite en el numero de visitas que puedes hacer por mes? Segun tu experiência se te llamara CRA II o Senior CRA, las vacantes son homebased pero si...
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Senior Cra Ii- Visitas On Site y Remotas
hace 2 días
Madrid, España NonStop Consulting A tiempo completoTengo un puesto como Senior CRA II single sponsor. Hay varias áreas terapéuticas entre las que puede elegir y también puede tener la opción de trabajar para un sponsor con varias áreas terapéuticas. Respecto a la promocion esta CRO promociona a los CRA muy rapido por lo que si quieres dar el salto a Line Manager o Project Manager esta es una buena...
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Cra Ii or Senior Cra
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Madrid, España ICON Plc A tiempo completoCRA II or Senior CRA ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Senior Clinical Research Associate (CRA) to join...
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Cra Ii
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Madrid, España ICON A tiempo completoAs a CRA sponsor dedicated, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. **What you will be 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...
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Cra Ii
hace 2 semanas
Madrid, España ICON A tiempo completoAs a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA manager the person ensures compliance of study conduct with ICH/GCP and country...
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Senior Cra Ii
hace 7 días
Madrid, España NonStop Consulting A tiempo completoEstoy trabajando con una de las mejores CRO a nível mundial para buscar a un Senior CRA para un solo sponsor. Hay muchas oportunidades de promocion interna ya que los managers siempre estan intentando promocionar a los empleados, ademas cualquiera que sea la progresion que quieras, sea a Project Manager o a otro tipo de puesto sera posible. Y puedes elegir...
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Cra Ii-madrid-sponsor-escoge El Área Terapéutica
hace 1 semana
Madrid, España NonStop Consulting A tiempo completoTengo un puesto de CRA II en el que puedes elegir el área terapéutica en la que trabajas. Est se debe a que nuestro cliente tiene varios sponsors y tendrán en cuenta tus preferencias, este es un puesto sponsor dedicated con sede en Madrid ya que los sponsors están ubicados en Madrid. Ademas, la empresa te intentara regionzalizar lo mas...
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Cra Spain-several Seniority Levels-cro
hace 1 semana
Madrid, España NonStop Consulting A tiempo completoTengo varias vacantes trabajar en una CRO mid siezed, buscan tanto perfiles de CRA II, CRA III y Senior CRA, y la vacante es homebased en cualquier parte de España, segun la experiência que tengas seras CRA II/III/Senior I/II/III. Ofrecen ademas flexibilidad en la fecha de inicio y horaria. **Responsabilidades**: Realizar visitas Administrar el protocolo...
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Senior Cra Ii
hace 2 días
Madrid, España NonStop Consulting A tiempo completoEstoy trabajando con una de las mejores CRO a nível mundial para buscar a un Senior CRA para un solo sponsor. Hay muchas oportunidades de promocion interna ya que los managers siempre estan intentando promocionar a los empleados, ademas cualquiera que sea la progresion que quieras, sea a Project Manager o a otro tipo de puesto sera posible. Y puedes elegir...
CRA II
hace 2 semanas
CRA II / Sr. CRA – Oncology Hybrid based. Oncology experience essential. Job Summary Roles within Clinical Monitoring/CRA are responsible for overseeing and ensuring the integrity of clinical research studies by monitoring data and processes from a centralized location. This includes conducting remote monitoring of trial sites to verify compliance with regulatory requirements and clinical protocols. Utilizes data analytics and risk-based monitoring techniques to identify potential issues and trends, ensuring that trials are conducted in accordance with established clinical practices. Collaborates with site teams to develop and implement tools, procedures, and processes that enhance quality monitoring and support the overall success of clinical trials. Responsibilities Perform site qualification, site initiation, interim monitoring, site management activities and close‑out visits (on‑site or remotely) ensuring regulatory, ICH‑GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance. Verify informed consent process and protect subject confidentiality, assessing safety and data integrity at investigator sites. Assess site processes, conduct source document review, verify CRF data accuracy, resolve inquiries, and support query resolution within agreed timelines. Perform investigational product inventory, reconciliation, and review of storage/security; ensure appropriate labeling, import/export, release/return. Review Investigator Site File accuracy, reconcile with Trial Master File, and advise on archiving requirements. Document activities and communicate via letters, reports, logs and other SOP‑compliant records; support recruitment, retention, and awareness strategies. Manage site‑level activities, budgets and timelines; adapt quickly to changing priorities and meet project objectives. Act as primary liaison with study site personnel, ensuring training and compliance; collaborate with central monitoring associates. Prepare for and attend investigator meetings, sponsor meetings, and global clinical monitoring/project staff meetings. Provide guidance towards audit readiness and support audit preparation and follow‑up actions. Maintain ICH/GCP and other regulatory knowledge, complete required training, and collaborate with sponsor affiliates, medical science liaisons, and local country staff. Impact & Contribution Individual contributors manage key components of projects, direct lower‑level professionals, and design, implement, or deliver processes and policies. The majority of time is devoted to process development, project management, and policy implementation using advanced education and experience. Qualifications Bachelor’s degree or RN in a related field or equivalent combination of education, training, and experience. Knowledge of Good Clinical Practice / ICH Guidelines and other applicable regulatory requirements. Strong computer skills and ability to embrace new technologies. Excellent communication, presentation, and interpersonal skills. Ability to manage required travel up to 75% on a regular basis. US ONLY: employee privacy notice compliance and confidentiality disclosure requirements. Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company is committed to compliance with the Americans with Disabilities Act, providing reasonable accommodations when appropriate. #J-18808-Ljbffr
