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Busco a alguien para que se encargue de las comidas (preparar los alimentos, servir y recoger) para un grupo de 11 nios.Los padres estarn presentes para solucionar cualquier problema.El men ser sencillo (fruta y verdura fresca, pasta con tomate y protenas simples como pechuga de pollo, salchichas o

It's a good feeling to know you're doing your best with purpose every day. At Artivion, we manufacture high-quality products and solutions for the treatment of aortic diseases. Together with surgeons worldwide, we save lives. In doing so, we rely on the strengths of each and every employee. Your strength counts, too: As an important link in the chain, you make a contribution to saving lives together with us. Bring your strengths and let us grow together. Solicitar este puesto es sencillo. Desplácese hacia abajo y haga clic en "Solicitar" para ser considerado para esta posición. We are hiring a Clinical Research Associate III – Home-Based in Spain (Spanish speaking candidates in France are also welcome) Your Strength Minimum of 4 years of advanced experience in clinical research monitoring In-depth knowledge of regulations and guidelines related to clinical trials involving human subjects (e.G., ISO 14155, GCP, MDR, EU, FDA) Ability to independently manage 10–15 study sites from start-up through close-out Excellent communication skills for site interaction, training, and issue resolution Strong collaboration and mentorship abilities, with a passion for supporting and guiding junior team members Hands-on experience with monitoring systems, source data verification, and compliance tracking Strong organizational skills with the ability to manage multiple priorities in a dynamic environment Willingness to travel regularly for site visits and investigator meetings across France and Spain Based in Spain (candidates from France may be considered in case a candidate lives nearby the Spain/France border and eager to do cross border monitoring) Fluent communication in English and Spanish (Catalan is preferred, French optional) Your Contribution Independently manage all phases of clinical trial site activities, including site identification, initiation, monitoring, and close-out Conduct monitoring visits in accordance with study protocols, GCP, and applicable regulatory requirements Act as the primary contact for investigational sites, ensuring compliance and providing ongoing support Build and maintain strong relationships with investigators, study coordinators, and site personnel Identify study risks, recommend solutions, and ensure timely resolution of site-related issues Perform source data verification and data review to ensure patient safety, protocol compliance, and data integrity Conduct site training, initiation visits, and support audit and inspection readiness Collaborate closely with Clinical Operations, Data Management, Medical Affairs, and other cross-functional teams Support investigator meetings, coordinator meetings, and deliver presentations or training sessions when required Mentor junior CRAs and contribute to process improvements and best practices Participate in CAPA activities, quality initiatives, audits, and continuous improvement efforts Our Strength A mission-driven company focused on saving lives International and collaborative MedTech environment Hybrid working model with flexibility Opportunities for growth and professional development Innovative products and meaningful clinical impact Contact Apply now and join the Artivion team. xhfqzwm We look forward to receiving your application documents in English through our online application system. Brian Russo T: JOTEC GmbH, a wholly owned subsidiary of Artivion, Inc. Lotzenäcker 23, 72379 Hechingen

It's a good feeling to know you're doing your best with purpose every day. At Artivion, we manufacture high-quality products and solutions for the treatment of aortic diseases. Together with surgeons worldwide, we save lives. In doing so, we rely on the strengths of each and every employee. Your strength counts, too: As an important link in the chain, you make a contribution to saving lives together with us. Bring your strengths and let us grow together. Solicitar este puesto es sencillo. Desplácese hacia abajo y haga clic en "Solicitar" para ser considerado para esta posición. We are hiring a Clinical Research Associate III – Home-Based in Spain (Spanish speaking candidates in France are also welcome) Your Strength • Minimum of 4 years of advanced experience in clinical research monitoring, • In-depth knowledge of regulations and guidelines related to clinical trials involving human subjects (e.G., ISO 14155, GCP, MDR, EU, FDA), • Ability to independently manage 10–15 study sites from start-up through close-out, • Excellent communication skills for site interaction, training, and issue resolution, • Strong collaboration and mentorship abilities, with a passion for supporting and guiding junior team members, • Hands-on experience with monitoring systems, source data verification, and compliance tracking, • Strong organizational skills with the ability to manage multiple priorities in a dynamic environment, • Willingness to travel regularly for site visits and investigator meetings across France and Spain, • Based in Spain (candidates from France may be considered in case a candidate lives nearby the Spain/France border and eager to do cross border monitoring), • Fluent communication in English and Spanish (Catalan is preferred, French optional) Your Contribution • Independently manage all phases of clinical trial site activities, including site identification, initiation, monitoring, and close-out, • Conduct monitoring visits in accordance with study protocols, GCP, and applicable regulatory requirements, • Act as the primary contact for investigational sites, ensuring compliance and providing ongoing support, • Build and maintain strong relationships with investigators, study coordinators, and site personnel, • Identify study risks, recommend solutions, and ensure timely resolution of site-related issues, • Perform source data verification and data review to ensure patient safety, protocol compliance, and data integrity, • Conduct site training, initiation visits, and support audit and inspection readiness, • Collaborate closely with Clinical Operations, Data Management, Medical Affairs, and other cross-functional teams, • Support investigator meetings, coordinator meetings, and deliver presentations or training sessions when required, • Mentor junior CRAs and contribute to process improvements and best practices, • Participate in CAPA activities, quality initiatives, audits, and continuous improvement efforts Our Strength • A mission-driven company focused on saving lives, • International and collaborative MedTech environment, • Hybrid working model with flexibility, • Opportunities for growth and professional development, • Innovative products and meaningful clinical impact Contact Apply now and join the Artivion team. xkdbapo We look forward to receiving your application documents in English through our online application system. Brian Russo T: JOTEC GmbH, a wholly owned subsidiary of Artivion, Inc. Lotzenäcker 23, 72379 Hechingen

ppBuscamos para una de nuestras clínicas de MADRID un/a ODONTOPEDIATRA que nos ayuden a que tanto hijos como padres vivan una experiencia inolvidable. MOONZ es un grupo internacional de clínicas especializadas en Ortodoncia para niños, en pleno proceso de expansión, y con único pensamiento: máxima calidad en los tratamientos haciéndolo divertido y educativo a nuestros pacientes y lo más agradable y sencillo posible a sus padres. Cumplimos los más altos estándares internacionales en tecnología, innovación y atención al paciente. /p pNuestro ingrediente secreto es la implicación que tiene el equipo en la educación de los niños durante el período del tratamiento, fomentando en ellos la creatividad, el desarrollo y la adquisición de buenos hábitos, dentro y fuera de la clínica. /p h3Requisitos: /h3 ul liGrado en Odontología /li liMáster Oficial de 2 años en Especialidad Odontopediatría (valorable) /li liExperiencia previa demostrable como Odontopediatra /li /ul h3Se ofrece: /h3 ul liPosición estable /li liPlan de carrera y desarrollo dentro de la compañía /li liContrato autónomo /li /ul pSi estás interesado en el proyecto Moonz, agradecemos que nos facilites el CV actualizado a los siguientes contactos: /p /p #J-18808-Ljbffr

MÉDICOS/AS ESPECIALISTA APARATO DIGESTIVO ONLINE VIDEOCONFERENCIA Solicitar este puesto es sencillo. Desplácese hacia abajo y haga clic en "Solicitar" para ser considerado para esta posición. En QSalud, centro médico enfocado en consultas online, ampliamos equipo y buscamos Aparato Digestivo interesados en un entorno de trabajo flexible y compatible con su práctica habitual. Responsabilidades - Evaluación y seguimiento de pacientes a través de videoconsulta o consulta telefónica. - Colaboración presencial ocasional en nuestro centro de Cuenca. Requisitos - Licenciatura/Grado en Medicina con especialidad en Aparato Digestivo (homologada en España). - Colegiación en España y Seguro de Responsabilidad Civil vigente. - Disponibilidad para acudir al menos un día al mes a Cuenca (con gastos cubiertos y remuneración atractiva). Qué ofrecemos - Incorporación ágil. - Colaboración en régimen mercantil (autónomo). - Flexibilidad total en la gestión de agenda. - Condiciones económicas competitivas por actividad presencial. xqysrnh Si estás interesado/a o conoces a alguien que encaje, estaremos encantados de hablar contigo. Contacto: Verónica Ruiz 623602430