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Experiencia y titulación en terapias manuales y en tratamientos de estética. Asesorar al cliente según sus necesidades tanto en tratamientos como en productos. Tareas de recepción: bienvenida y despedida del cliente.

Tu misión principal será ofrecer de manera cualificada las diferentes terapias de bienestar y tratamientos de masaje profesionales y atractivos para nuestros clientes.Ofrecer a los clientes los diferentes tratamientos corporales y faciales, así como masajes terapéuticos y de relax.Mantener la ca

Busco a alguien de confianza para acompañarme a mis citas médicas.Necesito apoyo para organizar la visita, recordar preguntas al médico y asistir durante la consulta si es necesario.Requiero que la persona sea amable, puntual y capaz de comunicarse en español.La visita podría durar entre 1 y 2

Busco a alguien confiable para acompañarme a una cita médica y ayudar con el traslado si es necesario.Soy una persona mayor/con movilidad reducida y me gustaría que la persona tenga paciencia, buena comunicación y experiencia en acompañamiento.La cita es en horario de mañana, con duración est

Quieres que tu vocación de cuidar transforme vidas en un entorno de máxima empatía?.Tiene su CV preparado? Si es así y confía en que este es el puesto ideal para usted, asegúrese de enviar su solicitud lo antes posible.Eres de esas personas que ven en la enfermería no solo una profesión, sin

Te incorporarás al laboratorio trabajando de forma muy estrecha con la Responsable del Laboratorio y Calidad, con el objetivo de asumir progresivamente mayores funciones y responsabilidad dentro del departamento. Oportunidad de evolucionar hacia una posición de referencia técnica dentro del labor

Modalidad: presencial en centro residencial. Capacidad para trabajar en coordinación con equipos sanitarios y educativos y para registrar actividad asistencial en soporte informático. Atender derivaciones médicas y realizar seguimiento psiquiátrico de las personas residentes.

No espere a enviar su solicitud después de leer esta descripción; se espera un gran volumen de candidaturas para esta oportunidad.Infermer / Infermera especialista en Infermeria del Treball.Som un servei de prevenció responsable, proper i equilibrat.Busquem persones que connectin amb aquests valo

En Clínica Diagonal buscamos Enfermeros y Enfermeras con experiencia en Servicios Especiales de Urgencias y UCI.

Assessor/a Genètic/a - Desenvolupa la teva carrera en un entorn clínic d'alt nivell.A continuación, encontrará un desglose completo de todo lo que se requiere de los posibles candidatos, así como la forma de presentar su candidatura.T'agradaria desenvolupar-te en un entorn hospitlaari de refer�

Descripción del empleo Para reforzar nuestro equipo ante una demanda en fuerte crecimiento, nuestra clínica dental busca un(a) Odontólogo(a) a tiempo completo o parcial y completar así su equipo dinámico, concienzudo y familiar. Inscríbase (haciendo clic en el botón correspondiente) después de revisar toda la información relacionada con el trabajo a continuación. • Tratamientos polivalentes (profilaxis, endodoncia, pequeñas intervenciones quirúrgicas, prótesis, etc.), • Posibilidad de colocar implantes (implantes: ETK o Biotech según los centros; biomateriales: Geistlich), • Posibilidad de tratar casos con alineadores si se cuenta con la formación adecuada (Invisalign y/o Smilers) Requisitos LO QUE LE OFRECE NUESTRA CLÍNICA • Atractiva retrocesión en función de su experiencia y especialidad, • Cartera de pacientes existente, • Auxiliares dentales dedicados, • Personal administrativo formado y polivalente, • Seguro médico y seguro de prevención sanitaria, • Reembolso del 50 % de los gastos de transporte público RAZONES PARA UNIRSE A NOSOTROS • Compañeros con un verdadero sentido de la ética y los valores humanos, • Personal dedicado a la gestión del consultorio (administrativo, material, mantenimiento, etc.), • Plataforma técnica de calidad (equipo radiográfico, cámara 3Shape o Medit, quirófano y motor de implantología), • Intercambio de conocimientos y experiencias entre compañeros, • Seguimiento de la formación continua DPC, • Formación interna y en colaboración xqysrnh con profesionales reconocidos en la profesión, • Programa de integración específico para profesionales junior: experiencia, asesoramiento y formación ¿Tienes un título en odontología de la Unión Europea ? ¿Tienes un nivel básico de francés (A2 / B1) y estás dispuesto a mejorarlo? ¿Te apetece la aventura Dentego ? Postula directamente a esta oferta o contáctanos a nuestra dirección de correo electrónico : Información adicional

Factorial is seeking a Senior Procurement Associate to lead and scale the procurement function across the Finance team. Haga clic en "Solicitar" a continuación para enviar su candidatura. Asegúrese de que su CV está actualizado y de que ha leído primero las especificaciones del puesto. You’ll manage the tech stack, negotiate contracts, and work with cross-functional teams to optimize spend and operations. xkdbapo In this role you’ll set purchasing strategy for multiple departments, oversee PO creation in NetSuite, and drive cost efficiencies while ensuring compliance and smooth vendor management. #J-18808-Ljbffr

Empresa del sector amplía su bolsa de empleo y precisa personal para el cuidado de personas mayores a domicilio por horas bajo el régimen de empleados del hogar.Es necesario acreditar experiencia laboral en este ámbito, contar con referencias telefónicas y disponer de la documentación en regla.

¿Buscas trabajo en ayuda a la dependencia? Este mes de julio surgen nuevas oportunidades para cuidadores en Canyelles. ¡Inscríbete gratis hoy mismo!

This job is with IBEC, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Introduction to the vacant position The Nanoprobes and Nanoswitches Group is looking for a Laboratory Technician to join an international and dynamic lab under the supervision of Silvia Pittolo. The contract will be within the framework of a Neuroscience research project using fiber photometry in freely-moving mice aimed at studying how antidepressant treatment alters brain neuromodulatory signals. Main Tasks and Responsibilities - Perform includes animal surgery for AAV delivery - Conduct fiber photometry recordings and behavior in freely-moving mice - Simultaneous recordings of brain signaling molecules via fluorescent biosensors - Histological analysis of brain tissue - Data analysis and interpretation - Communication of results Knowledge, Skills, and Abilities Essential: - Degree in Biology, Biotechnology, Biomedical Engineering, or related field - Passion for Neuroscience research with a focus on psychiatric and neurodevelopmental disorders - Committed to purse a PhD in Neuroscience, Biomedicine, or related by applying to private and public doctoral fellowships - Independent, critical thinking and problem-solving attitude - Excellent communication and teamwork - Research integrity - Fluent English Desirable: - Accreditation to perform experiments in laboratory mice (FELASA or similar) - Experience with mouse surgeries, manipulation - Experience in brain histology (intracardial perfusion, IHC and smFISH) - Coding experience (Matlab/python) We Offer - Number of available positions: 1 - Starting date: 01/09/2026 - Working conditions: - Full time (37.5 hours/week), 1-year initial contract - Open-ended contract for scientific and technical activities, linked to the project and budget duration. - Competitive salary - Measures to reconcile work and family life (parental leave, flexible schedule working hours, 23 working days of paid holidays, 9 leave days for personal matters, among others). - Full access to IBEC's training catalogue (hard and soft skills for researchers, including tech transfer, grant writing, transition to industry, and more) - Access to IBEC's mentoring program for predoctoral researchers. - IBEC ensures equality of access to professional development opportunities irrespective of employment status, length at IBEC or other factors. The IBEC's yearly training catalogue offers a wide range of training in technical and transferable skills including mobility grants and a Mentoring programme for predoctoral and postdoctoral researchers. - Stimulating, interdisciplinary research and high-quality international scientific environment. - Induction programme to facilitate incorporation at IBEC and additional support is provided for foreigners to obtain Visa-working permit and to install in Barcelona. How to apply Until 08/08/2026 An online application form is available through IBEC's dedicated site: Only applications submitted before the deadline will be evaluated. Reference: LT-SP If you have any further question regarding your application, please contact us at jobs@ibecbarcelona.eu Principles of the selection process: IBEC is committed to the principles of the Code of Conduct for the Recruitment of Researchers of the European Commission and the Open, Transparent and Merit based Recruitment principles (OTM-R) IBEC ́s Commitment on equal opportunity, diversity, and Inclusion: Our strength and excellence as an international transdisciplinary Research Institute are based on diversity. Being an equal opportunity employer, we are committed to diversity and inclusion, so that we support employees irrespective of their gender, nationality, religion, disabilities, age, sexual identity or cultural and socioeconomic background. Visit our devoted webpage on Equality, Diversity and Inclusion. For candidates with children that come from outside Barcelona, we offer babysitting services during the interview, so you don't have to worry about anything else than doing a good interview. Contact us if you are interested in this service. In categories where women are underrepresented, such as Group Leader positions, and with the aim of ensuring gender balance in recruitment processes, women candidates must represent at least 50% of those interviewed for Junior-level positions and 40% for Senior-level positions, provided they have CVs comparable to those of male candidates. At the end of the evaluation process, in cases of equal merit, preference will be given to women candidates. IBEC, as a signatory of the San Francisco Declaration on Research Assessment (DORA), will consider, especially for early-stage investigators, much more the scientific content of research outputs, than publication metrics or the identity of the journal in which it were published. Protection of personal data: IBEC guarantees that candidates' personal data are processed in accordance with the requirements of the EU General Data Protection Regulation (GDPR) and Law 3/2018 on Data Protection. Personal data will be processed solely for the purposes of the selection process. Who we are? The Institute for Bioengineering of Catalonia, IBEC is an interdisciplinary research center focused on Bioengineering and Nanomedicine based in Barcelona. IBEC is one of the top research institutions named as a Severo Ochoa Research Centre by the Ministry of Science, Universities and Innovation, which recognizes excellence at the highest international level in terms of research, training, human resources, outreach and technology transfer. IBEC's mission is to develop international high-quality interdisciplinary research that, while creating knowledge, contributes to making a better quality of life, improving health and creating wealth. A close link with key universities, reference hospitals and corporations, are assets that facilitate achieving the mission. IBEC was established in 2005 by the Generalitat de Catalunya (Autonomous Government of Catalonia), the University of Barcelona (UB) and the Technical University of Catalonia (UPC). IBEC is located within the Barcelona Science Park and UPC Besós Campus, with an annual budget of 21 Mio€; 4.400 square meters of facilities; 25 research groups and a team of researchers and support services of 450 people from 40 different countries. www.ibecbarcelona.eu Share this... FacebookPinterestTwitterLinkedin

Experteer Overview As Associate Clinical Project Management Director, you will lead and oversee studies to ensure timely, high-quality delivery within contracts. You’ll work with cross-functional teams to implement study strategies, manage risks, and drive financial performance. You will own relationships with key customers and guide the team to achieve milestones across multi-country studies. This role offers impact in shaping immuno-oncology and cell/gene therapy programs at IQVIA, with a hybrid work setup and strong emphasis on leadership and collaboration. Compensaciones / Beneficios • Lead bid defense preparations and presentations with Business Development for large, multi-country studies • Develop or support integrated study management plans with the core project team • Oversee strategic delivery of clinical studies, optimizing speed, quality, and cost • Serve as primary project liaison with customers and coordinate with IQVIA BD as needed • Set objectives for the project team, monitor performance, and provide leadership feedback • Collaborate with functional groups to achieve milestones and manage issues • Monitor progress, communicate proactively to stakeholders, and manage risks and contingencies • Coach and mentor junior team members to ensure global alignment and development • Ensure study quality, manage quality risks, and implement CAPAs as needed • Participate in executive committees as part of program leadership • Ensure financial success through resource management, forecasting, and profitability • Forecast opportunities, accelerate activities, and manage scope changes with customer agreement • Capture lessons learned and promote continuous improvement • Support corporate initiatives and act as a change advocate • Provide input on team members’ performance and support staff development Responsabilidades • Bachelor’s degree in life sciences or related field with advanced knowledge of role • 10+ years of clinical research experience, including 6+ years in project management • Knowledge of clinical trials, regulatory requirements (ICH GCP, local laws) and protocol understanding • Strong communication, presentation, negotiation, and customer management skills • Problem solving, leadership, and organizational planning capabilities • Ability to manage priorities, strategic thinking, and cross-functional collaboration • Attention to quality, learning agility, and up-to-date knowledge • Proficiency with MS Office (Word, Excel, PowerPoint) and IT literacy • Experience in managing project finances, contracts, and change control • Ability to work across geographies and understand cultural differences Requisitos principales • Hybrid work model

Experteer Overview As a Principal Biostatistician, you lead statistical activities across studies, mentor biostatisticians, and shape study design and analysis. You will serve as the statistical contact for sponsors, oversee training, and ensure timely, high-quality deliverables. The role involves collaboration with cross-functional teams, regulatory interfaces, and contributing to proposals and budgets. This opportunity offers impact across programs and a path into a future live role within a global biostatistics team. Compensaciones / Beneficios • Serve as a statistical department resource and mentor statisticians • Prepare Statistical Analysis Plans (SAPs) and mock-ups for tables, listings, and figures • Handle statistical aspects of protocols and randomization input to clinical study reports • Review SAS CRFs, SAS database design, and study documentation for data quality • Create or review programming specs for analysis datasets, tables, listings, and figures • Direct and review work of biostatistics personnel to ensure timely, high-quality output • Contribute to company objectives and develop alternative solutions for operational challenges • Act as biostatistics representative on project teams and prepare for internal meetings • Ensure verification/quality control of deliverables and alignment with SAPs and specs • Manage multi-project scheduling, milestones, and time estimates; escalate when needed • Provide statistical programming support as needed • Participate in DSMB/DMC activities and possibly act as independent or voting statistician • Lead projects with integrated analyses and support regulatory meetings • Ensure SOPs, WIs, and regulatory guidelines are followed • Maintain organized project documentation and inspection readiness • Support business development through proposals and sponsor bid defenses • Perform other duties as assigned • Occasional travel; this posting may be for future opportunities Responsabilidades • Strong statistical leadership in clinical trials with experience guiding teams • Proven ability to develop SAPs and statistical plans • Experience with randomization, protocol input, and clinical study reports • SAS-based programming and review of CRFs and database design • Ability to manage multiple projects and deadlines; proactive communication • Exposure to DSMB/DMC processes and regulatory interactions • Knowledge of SOPs, WIs, and ICH guidelines • Experience with collaboration across sponsors and internal teams • Quality control and documentation management skills • Willingness to contribute to proposals and business development • Minimal travel as needed Requisitos principales • career development and progression • Total Self culture • supportive line management • technical and therapeutic area training • peer recognition • total rewards program

BUSCAMOS UN/A MÉDICO/CA GENERAL PARA FORMAR PARTE DE NUESTRO EQUIPO INTERDISCIPLINARIO EN UN CENTRO ESPECIALIZADO EN LA ATENCIÓN A PERSONAS CON DISCAPACIDAD INTELECTUAL (DI) Y TRASTORNO DEL ESPECTRO AUTISTA (TEA). SU FUNCIÓN PRINCIPAL SERÁ LA EVALUACIÓN, DIAGNÓSTICO Y TRATAMIENTO DE LOS TRASTORNOS SOMÁTICOS Y AGITACIONES CONDUCTUALES URGENTES DE LOS USUARIOS, COLABORANDO CON OTROS PROFESIONALES PARA OFRECER UNA ATENCIÓN INTEGRAL, ASÍ COMO LA PREVENCIÓN Y PROMOCIÓN DE LA SALUD. Datos de contacto: CÓDIGO DE OFERTA: 092026022130 La inscripción a esta oferta se efectúa a través del portal Feina Activa (https://feinaactiva.gencat.cat/web/guest/home ), donde encontrará más información sobre los detalles del puesto de trabajo. Puede acceder a la oferta indicando la referencia (Referencia número:92320796) en la búsqueda avanzada de Feina Activa. Para optar a las ofertas de este portal, se precisa una inscripción previa en él.

Centro sanitario privado, solicita incorporar un cirujano maxilofacial y un médico dermatólogo para colaborar en las áreas médicas. Jornadas y condiciones a convenir. Envía Currículum y disponibilidad.

Experteer Overview En Telefónica Tech, te incorporarás a la unidad de Ciberseguridad y Respuesta a Incidentes para proteger activos críticos ante amenazas digitales. Trabajarás en un entorno internacional y con equipos multidisciplinarios, identificando y respondiendo a incidentes en tiempo real. Implementarás prácticas de ciberseguridad, propondrás mejoras de políticas y colaborarás con N1 y N3 para minimizar impactos. Buscamos a alguien proactivo, analítico y orientado a la mejora continua que quiera contribuir a la seguridad de clientes y operaciones. Oportunidad de trabajar con tecnologías avanzadas y crecer en un entorno dinámico y colaborativo. Compensaciones / Beneficios • Monitorizar alertas de seguridad (SIEM, EDR, IDS/IPS) • Analizar y priorizar incidentes, identificando impacto y origen • Ejecutar planes de contención, erradicación y recuperación • Colaborar en investigaciones de incidentes complejos • Generar informes de eventos y tendencias • Proponer mejoras a políticas y procedimientos de ciberseguridad • Escalar incidentes a N3 cuando sea necesario • Mantener indicadores de compromiso (IoCs) actualizados • Participar en simulaciones de respuesta a incidentes Responsabilidades • Más de 2 años en análisis de ciberseguridad, gestión de incidentes y operaciones SOC/CERT • Experiencia en entornos de alta criticidad • Conocimientos en análisis forense digital, ciberinteligencia, hacking ético y análisis de malware • Familiaridad con marcos y estándares de seguridad (NIST, ISO 27001, MITRE ATTu0026CK) • Experiencia con herramientas SIEM (Splunk, QRadar) y soluciones EDR/XDR • Formación en Ingeniería técnica Informática o superior, Telecomunicaciones o equivalente • Certificaciones relevantes (GCFA, GCFE, CEH, CompTIA Security+ o similar) • Conocimientos de configuración y análisis de herramientas de seguridad (SIEM, IDS/IPS, EDR, firewalls, WAF) • Adquisición y análisis de artefactos forenses (KAPE, Velociraptor, Eric Zimmerman, Sysinternals, Nirsoft, xways, Wireshark, tcpdump) • Identificación de IoCs y análisis de TTPs • Scripting para automatización (Python, PowerShell, Bash) • Gestión de vulnerabilidades y análisis de riesgos Requisitos principales • Medidas de conciliación y flexibilidad horaria • Formación continua y certificaciones • Modelo híbrido de teletrabajo • Paquete de beneficios sociales • Ambiente de trabajo dinámico y multidisciplinar • Programas de voluntariado

Experteer Overview En Telefónica Tech, te incorporas a la unidad de Ciberseguridad y Respuesta a Incidentes para identificar, analizar y responder ante incidentes de seguridad en tiempo real. Trabajarás con equipos N1 y N3 y gestionarás alertas de seguridad, priorizando incidentes y ejecutando planes de contención y recuperación. Colaborarás en investigaciones complejas y contribuirás a mejorar políticas de ciberseguridad. Es una oportunidad para impactar en la protección de activos críticos a través de prácticas avanzadas y herramientas de seguridad. Compensaciones / Beneficios • Monitorizar y gestionar alertas de seguridad (SIEM, EDR, IDS/IPS) • Analizar y priorizar incidentes, identificando impacto y origen • Ejecutar contención, erradicación y recuperación de incidentes • Colaborar en investigaciones con equipos internos/externos • Generar informes sobre eventos, incidentes y tendencias • Proponer mejoras a políticas y procedimientos de ciberseguridad • Escalar incidentes a N3 cuando sea necesario • Actualizar y mantener indicadores de compromiso (IoCs) • Participar en simulaciones de respuesta a incidentes y ejercicios de ciberseguridad Responsabilidades • Más de 2 años en análisis de ciberseguridad, gestión de incidentes y operaciones de SOC/CERT • Experiencia en entornos de alta criticidad • Conocimientos en análisis forense digital, ciberinteligencia y técnicas de hacking ético y análisis de malware • Conocimientos de marcos y estándares (NIST, ISO 27001, MITRE ATTu0026CK) • Experiencia en SIEM (Splunk, QRadar) y soluciones EDR/XDR • Titulación en Ingeniería técnica Informática o superior (equivalente) • Certificaciones relevantes como GCFA, GCFE, CEH, CompTIA Security+ (deseables) • Conocimientos de herramientas de seguridad (SIEM, IDS/IPS, EDR, firewalls, WAF) Requisitos principales • Medidas de conciliación y flexibilidad horaria • Formación continua y certificaciones • Modelo híbrido de teletrabajo • Paquete de beneficios sociales • Excelente ambiente de trabajo dinámico y multidisciplinar • Programas de voluntariado

Experteer Overview In this role you lead complex, global clinical trials from start-up to close-out, driving quality, timelines, budgets, and regulatory alignment. You will partner with sponsors and cross-functional teams to deliver multi-regional studies that advance innovative medicines. The position emphasizes strategic leadership, risk management, and stakeholder engagement in a fast-paced, data-driven environment. You’ll contribute to shaping clinical research at scale and work with industry-leading sponsors. Compensaciones / Beneficios • Lead delivery of complex global/multi-regional studies and drive operational excellence • Serve as primary strategic sponsor partner, offering leadership and innovative solutions • Provide direction to cross-functional teams across regions for collaboration and high performance • Oversee timelines, budgets, quality, risks, and operational delivery to successful study outcomes • Drive proactive risk management, issue resolution, and stakeholder alignment throughout study lifecycle • Ensure adherence to ICH-GCP, regulatory requirements, and contractual commitments Responsabilidades • Bachelor's degree in Life Sciences, Healthcare or related field • 7+ years of clinical research experience with global or multi-regional trials in CRO/pharma/biotech • Strong knowledge of clinical trial conduct, ICH-GCP guidelines and regulatory requirements • Proven track record leading cross-functional teams and managing study delivery (timelines, budgets, quality, risks) • Demonstrated ability to build trusted sponsor relationships and manage senior stakeholders in a global setting • Exceptional leadership, communication, problem-solving and decision-making skills • Passion for advancing clinical research and patient outcomes Requisitos principales •

Compensaciones / Beneficios • Captación de oportunidades identificando nuevos clientes • Asesorar a propietarios en el proceso de compraventa de farmacias • Gestión de cartera y relaciones comerciales con propuestas a medida • Colaborar en estrategias comerciales y seguimiento de resultado

Aristocrat, a global leader in entertainment tech, is seeking a Business Analyst for its Ad Tech team in Barcelona. Compruebe a continuación si tiene lo necesario para esta oportunidad y, si es así, envíe su solicitud lo antes posible. You will support Growth with operational marketing analytics, manage partner platforms, and ensure accurate campaign tracking and reporting. This role connects User Acquisition, Marketing, external partners, and centralized Data Analytics teams. xkdbapo You will oversee dashboards, validate data, and help translate business requirements into data requests while collaborating across data #J-18808-Ljbffr Hay opciones de teletrabajo/trabajo desde casa disponibles para este puesto.

¿Buscas trabajo en ayuda a la dependencia? Este mes de julio surgen nuevas oportunidades para trabajadores y educadores sociales en Sarria. ¡Inscríbete gratis hoy mismo!

A ACS INFORMàTICS ESTEM SELECCIONANT UN TèCNIC/A DE SUPORT AL LLOC DE TREBALL PER INCORPORAR-SE A UN PROJECTE ESTABLE DE LA GENERALITAT DE CATALUNYA, DONANT SERVEI A L'àMBIT SANITARI DEL CENTRE DE TELECOMUNICACIONS I TECNOLOGIES DE LA INFORMACIÓ . LA PERSONA SELECCIONADA DESENVOLUPARà LA SEVA ACTIVITAT DE MANERA PRESENCIAL A L'HOSPITAL UNIVERSITARI DE BELLVITGE (BARCELONA), OFERINT SUPORT TèCNIC ALS USUARIS I GARANTINT EL CORRECTE FUNCIONAMENT DELS EQUIPS I SERVEIS INFORMàTICS. Datos de contacto: CÓDIGO DE OFERTA: 092026022248 La inscripción a esta oferta se efectúa a través del portal Feina Activa (https://feinaactiva.gencat.cat/web/guest/home ), donde encontrará más información sobre los detalles del puesto de trabajo. Puede acceder a la oferta indicando la referencia (Referencia número:92320891) en la búsqueda avanzada de Feina Activa. Para optar a las ofertas de este portal, se precisa una inscripción previa en él.

Experteer Overview As a Senior Tech TA Partner in SumUp’s Barcelona hub, you’ll own the end-to-end hiring for Engineering, Product, Data, and Design within Banking and Lending. You’ll shape hiring strategy, build and maintain strong relationships with hiring managers, and lead data-driven sourcing to scale core fintech products. You’ll engage with the Barcelona tech scene to position SumUp as an employer of choice and ensure an exceptional candidate experience. This role offers impact at scale in a fast-moving fintech environment. Compensaciones / Beneficios • Own end-to-end hiring for Engineering, Product, Design, and Data roles • Build trusted advisor relationships with hiring managers in Banking and Lending • Lead regular hiring cadences and maintain pipeline visibility • Create market maps of Spain's tech ecosystem to fuel sourcing • Champion SumUp’s presence in the Barcelona tech scene and networks • Track funnel health metrics and provide actionable recommendations • Create an inclusive, candidate-centric hiring process Responsabilidades • Proven track record in full-cycle TA for Engineering, Product, Data, and Design in fast-moving environments • Strong understanding of the Spanish and EU tech talent market • Expertise in advanced sourcing, market mapping, and diverse top-of-funnel strategies • Ability to advise on market realities, drive prioritization, and calibrate interviews • Experience using funnel analytics and market insights to inform hiring strategies • Genuine care for an outstanding candidate experience • English fluency; international team experience Requisitos principales • virtual stock option programme • annual Lu0026D budget of 2000 • 23 days of paid leave • subsidised restaurant tickets • Break4me sabbatical after 3 years • referral bonus

Experteer Overview As Clinical QA Manager, you will lead robust clinical quality assurance oversight at country and site levels. You will shape QA strategies, drive risk-based compliance, and safeguard patient safety and data integrity in collaboration with global and regional stakeholders. You’ll assess and audit processes, guide teams on quality policies, and help prepare for inspections. This role offers impact by strengthening quality management systems and enabling faster access to medicines within a values-driven culture. Compensaciones / Beneficios • Develop and implement QA strategies to support clinical trial activities • Conduct quality assessments and audits to ensure regulatory compliance • Collaborate with project teams to identify issues and implement corrective actions • Provide guidance on QA policies, procedures, and best practices to staff • Contribute to development and maintenance of quality management systems and documentation Responsabilidades • Bachelor's degree in relevant discipline • Minimum 5 years' QA experience in pharmaceutical, biotechnology, or CRO • Knowledge of regulatory requirements for clinical trials (ICH-GCP, FDA) • Strong analytical and problem-solving skills • Excellent communication and interpersonal skills, with cross-functional collaboration ability • Willingness to travel ~35% • Legal right to work in the country of employment Requisitos principales • Competitive base salary • Health and wellbeing programmes (medical, dental, vision) • Retirement and pension plans • Life assurance and disability coverage • Employee assistance programmes and wellbeing resources • Learning and development opportunities

OFRECEMOS CONTRATO DE TRABAJO O COLABORACIÓN. TÚ YO PSICÓLOGOS LGTBIQ+ ,ESPECIALIZADOS EN ATENCIÓN PSICOLÓGICA A PERSONAS DEL COLECTIVO LGTBIQ+ Y SU ENTORNO. TRABAJAMOS DESDE UNA PERSPECTIVA INCLUSIVA, LIBRE DE PREJUICIOS Y RESPETUOSA CON TODAS LAS IDENTIDADES Y ORIENTACIONES. APOSTAMOS POR UN AMBIENTE DE TRABAJO CERCANO, CUIDADO Y SEGURO TANTO PARA EL EQUIPO COMO PARA LAS PERSONAS QUE ATENDEMOS. Datos de contacto: CÓDIGO DE OFERTA: 092026023114 La inscripción a esta oferta se efectúa a través del portal Feina Activa (https://feinaactiva.gencat.cat/web/guest/home ), donde encontrará más información sobre los detalles del puesto de trabajo. Puede acceder a la oferta indicando la referencia (Referencia número:92321531) en la búsqueda avanzada de Feina Activa. Para optar a las ofertas de este portal, se precisa una inscripción previa en él.

Experteer Overview In this role you will lead the scientific strategy across global clinical development programs in neuroscience, driving translational insight into clinical execution and regulatory strategy. You collaborate with cross-functional teams and external experts to shape high-impact programs that advance innovative therapies to patients worldwide. You’ll influence regulatory submissions, safety monitoring, and decision-making across development lifecycles in a dynamic, collaborative environment. This is a chance to shape the future of medicine with a global organization committed to patient outcomes and scientific excellence. Compensaciones / Beneficios • Provide clinical leadership and strategic medical input across global clinical development programs • Lead development of clinical sections for regulatory submissions, briefing documents, and investigator materials • Drive execution of clinical programs in partnership with trial leaders and cross-functional global teams • Oversee trial data review, interpretation, and reporting including CSR and publications • Support benefit-risk assessment and safety monitoring with patient safety teams • Engage with regulatory authorities, key opinion leaders, and advisory boards • Contribute to clinical strategy, standards development, and global initiatives across development functions Responsabilidades • Medical degree • Specialization in Neuromuscular or Neuroscience/Neurodegeneration and/or Movement disorders • Experience in Gene Therapy research, especially CAR-T (highly desirable) • Several years in clinical research or global drug development across early and late phases • Proven experience leading or contributing to global clinical trials (planning, execution, reporting) • Strong knowledge of trial methodology, regulatory requirements, and GCP • Ability to analyse and communicate complex clinical data • Experience working in global, cross-functional, matrixed environments with diverse stakeholders • Strong leadership, collaboration, and communication skills to influence senior stakeholders Requisitos principales •

Experteer Overview In this Manager role, you oversee a portfolio of patient-centered research projects and translate findings into strategic client recommendations. You work closely with senior leaders and manage client relationships across multiple projects, guiding junior teammates and shaping evidence generation for regulatory and market access. You’ll collaborate with scientific colleagues to design studies, integrate results into actionable insights, and contribute to business development. The position blends scientific rigor with client impact in a global, fast-paced environment. Compensaciones / Beneficios • Manage a portfolio of consulting projects with delivery and client relationship accountability • Coach and direct junior team members • Develop knowledge of patient science for evidence generation and dissemination, regulatory and market access strategy • Partner with scientific colleagues to design study materials and conduct patient-centered research • Integrate research outputs into strategic recommendations • Create reports, presentations and facilitate workshops • Contribute to business development and assist with proposal development • Support people-related activities such as recruitment, training and development • Lead initiatives in knowledge management and process improvement • Mentor 1–3 junior team members Responsabilidades • Advanced academic science degree in public health, epidemiology, psychology, sociology, medical anthropology, health economics or related field • Minimum 5 years of experience in at least one of the stated fields • Experience in strategic consulting and project management • Exposure to COA/PRO, patient preference and/or real-world evidence methods • Advanced knowledge of healthcare regulatory processes and international payer systems • Excellent written and verbal communication, including presentations and report writing • Strong analytical, interpretative, and problem-solving skills • Excellent interpersonal skills and ability to work with others • Ability to work in a fast-paced environment and manage multiple tasks • Ability to work in multi-disciplinary, international teams Requisitos principales •

Experteer Overview In this role you drive clinical trial delivery and oversight within ICON, coordinating cross-functional activities to ensure high-quality outcomes. You mentor CRAs, manage trial start-up and enrollment, and safeguard study integrity while fostering strong relationships with sponsors and vendors. You operate in a global context, solving complex problems and scaling operations to support faster patient access to new medicines. This is a values-driven opportunity to shape trials and build high-performing teams. Compensaciones / Beneficios • Budget oversight to allocate resources efficiently • Develop monitoring plans and ensure robust study oversight • Train and mentor Clinical Research Associates to improve performance • Lead study start-up and enrollment, adhering to timelines • Review trip reports and implement CAPAs to improve study integrity • Foster productive relationships with Sponsors, vendors, and cross-functional teams Responsabilidades • 4+ years of clinical trial management experience at a CRO or pharmaceutical organization • Bachelor's degree in health, life sciences, or related field • At least 10+ years of relevant experience in clinical trial management • Preferred: 2+ years of monitoring experience • Experience in managing complex or global trials is advantageous • Experience in managing all trial components from start-up to database lock is preferred • Experience in coaching/mentoring CTMs and leading a team of CTMs • Willingness to travel ~25% Requisitos principales • Competitive base salary and performance-related incentives • Health, dental, and vision coverage where applicable • Retirement and pension plans • Life assurance and disability coverage • Employee assistance programmes and wellbeing resources • Learning and development opportunities

Se seleccionan odontólogos/as con experiencia para trabajar en clínicas de Galicia, Asturias, Castilla y León, Cantabria, País Vasco y La Rioja.Con posibilidad de cambio de residencia e incorporación inmediata.Envía tu Currículum y provincia de preferencia.

Experteer Overview In this role you drive strategic sourcing for Sanofi’s Digital domain, shaping category strategies and negotiations to deliver best-in-class savings. You’ll partner with Global Buyers and stakeholders to optimize the global procurement footprint, advance BOI improvements, and foster data-driven supplier partnerships. The position blends leadership, cross-functional collaboration, and strategic thinking to support Sanofi’s mission of delivering breakthrough medicines. This is a global, high-impact role located in Barcelona with a hybrid work model. Compensaciones / Beneficios • Build and execute sourcing initiatives aligned with budgets and long-range plans • Define and implement category strategies in collaboration with category managers • Lead global negotiations to optimize BOI and value, coordinating with stakeholders • Share supplier market knowledge and explore new suppliers, technologies, substitution products • Achieve savings targets and maintain a robust savings pipeline • Coach Global Buyers on sourcing strategies, tactics, and market knowledge • Communicate ongoing sourcing activities proactively within and outside the Domain • Engage with other Procurement Domains to leverage shared services • Manage supplier relationships with business reviews and performance management • Ensure mastery of procurement technical excellence (TCO, SRM, Market Intel, Risk, CSR, HSE, compliance) • Work with procurement services to leverage middle and back-office support • Engage upfront with key Digital stakeholders and other GBUs • Present procurement strategies to internal customers for input Responsabilidades • +5 years experience in Procurement or related field • Master degree from an accredited college or university • Fluent in English • Strong negotiation skills and mastery of negotiation techniques • Strategic thinking and innovative approach to business solutions • Good understanding of business operations, legal aspects, SLAs, KPIs • Strong analytical, problem-solving, and communication skills • Experience managing complex, multi-functional matrix organizations • Transversal management skills and high ethical standards Requisitos principales • employee benefit programs • hybrid work arrangement

¿Buscas trabajo en ayuda a la dependencia? Este mes de julio surgen nuevas oportunidades para auxiliares de enfermería en Barcelona. ¡Inscríbete gratis hoy mismo!

Novartis is seeking an Associate Director to lead a Barcelona-based team shaping the next generation of clinical data capabilities. Descubra más sobre las tareas diarias, las responsabilidades generales y la experiencia requerida para esta oportunidad desplazándose hacia abajo ahora. The role connects business, science, data and technology to improve trial delivery, data quality, and patient outcomes. xohynlm The position is hybrid with 12 onsite days per month at Barcelona Gran Via. You will mentor Talent in RBQM, analytics and digital solutions across Global Clinical Operations. #J-18808-Ljbffr

Se seleccionan odontólogos/as con experiencia para trabajar en clínicas de Galicia, Asturias, Castilla y León, Cantabria, País Vasco y La Rioja.Con posibilidad de cambio de residencia e incorporación inmediata.Envía tu Currículum y provincia de preferencia.

Experteer Overview En Quirónsalud, Hospital Universitari Sagrat Cor, buscas un especialista en anestesia para brindar atención de alta calidad en diversas cirugías y colaborar en la mejora continua de los servicios.Formarás parte de un hospital de segundo nivel con vocación investigadora y do

Experteer Overview In this Principal Biostatistician role, you lead biomarker statistics across studies, shaping analytical plans and collaborating with cross-functional teams to advance biomarker research in clinical development. You will drive planning, execution, and interpretation of genomic and biomarker analyses, including RNA and related data, with an emphasis on rigor and independent leadership. You’ll leverage AI/ML approaches to enhance decision-making and contribute to Biomarker Evaluation Reports. This role focuses on biomarker data in a fast-paced, collaborative environment across Europe. Compensaciones / Beneficios • Plan, execute and analyze biomarker (including genomics) aspects of clinical or biomarker studies as the project biomarker statistician • Develop Biomarker Evaluation Plans ensuring consistency across projects • Provide statistical input in clinical development discussions and AI/ML usage • Coordinate statistical activities for biomarker Ru0026D across studies and projects • Conduct advanced data analysis for genomics and biomarker stats, including programming and complex algorithms • Handle RNA, olink and other biomarker data • Ensure production and accuracy of Biomarker Evaluation Reports and statistical deliverables • Work independently on routine and complex statistical questions and tasks • Develop and implement standard processes for biomarker analyses Responsabilidades • PhD or MSc in Biostatistics, Statistics or Mathematics, or related field • Strong communication and interpersonal skills • Ability to work independently and in teams; minimal supervision required • Experience with AI and ML approaches • Previous independent biomarker study leadership • Previous clinical trial or industry experience preferred • Strong knowledge of biomarker evaluation, particularly in immunology and infections, type I diabetes • Proficiency in statistical programming languages R (Bioconductor) and Python • Experience with high-dimensional data analysis Requisitos principales •

Experteer Overview In this role you will design and deliver TMF and CDGM learning programs to strengthen compliance and TMF health. You will partner with cross-functional teams to identify learning needs and implement knowledge solutions that scale across the organization. You’ll develop metrics to measure learning impact and act as SME for TMF processes, contributing to audit readiness and ongoing process improvements. This is a chance to drive capability building in a global, collaborative environment and help accelerate transformative therapies to patients. Compensaciones / Beneficios • Design and deliver learning and capability programs for TMF and CDGM services • Identify learning needs across functions and implement tailored knowledge solutions • Develop dashboards and KPIs to monitor learning effectiveness • Collaborate with internal teams and external partners on CDGM learning requirements • Serve as SME on TMF learning processes, tools, and capability development • Drive initiatives to improve TMF health and adoption of documentation standards • Support audit and inspection readiness, including root cause analysis and CAPAs • Coordinate with enterprise learning groups to align with best practices • Act as CDGM liaison for projects ensuring alignment with business initiatives • Create and manage knowledge management frameworks for continuous learning and improvement Responsabilidades • Bachelor’s degree or equivalent with relevant industry experience • Minimum five years in clinical research within pharma companies or CROs • Experience in clinical documentation, records management, or information management • Proven ability to plan and execute cross-functional projects • Strong communication, influencing, and presentation skills across all levels • Demonstrated ability to collaborate across global, cross-cultural, multidisciplinary teams Requisitos principales • insurance plans • retirement plans • wellbeing resources • global recognition programs • flexible and hybrid working options • minimum 14 weeks paid parental leave

T?AGRADA CUIDAR I MILLORAR LA QUALITAT DE VIDA DE LES PERSONES GRANS? VOLS FORMAR PART D?UN EQUIP HUMà, PROFESSIONAL I EN CONSTANT CREIXEMENT? AQUESTA ÉS LA TEVA OPORTUNITAT! Datos de contacto: CÓDIGO DE OFERTA: 092026021733 La inscripción a esta oferta se efectúa a través del portal Feina Activa (https://feinaactiva.gencat.cat/web/guest/home ), donde encontrará más información sobre los detalles del puesto de trabajo. Puede acceder a la oferta indicando la referencia (Referencia número:92320499) en la búsqueda avanzada de Feina Activa. Para optar a las ofertas de este portal, se precisa una inscripción previa en él.

Experteer Overview In this role you will oversee end-to-end clinical trial operations in oncology, driving high-quality outcomes across programmes. You will work with cross-functional teams and investigators to implement protocols, ensure compliance, and manage timelines, budgets, and risk. The position anchors relationships with trial sites and stakeholders while navigating regulatory and ethical guidelines. You will help shape trial design decisions and vendor selections, contributing to ICON’s mission to bring new medicines to patients faster. This role offers a hands-on, impactful opportunity in a collaborative, values-driven environment. Compensaciones / Beneficios • Plan and manage all aspects of clinical trials, ensuring timelines, budget, and quality standards are met • Collaborate with cross-functional teams to implement trial protocols and procedures • Build and maintain strong relationships with trial investigators and stakeholders • Ensure trials comply with local, national, and international regulations and ethical guidelines • Problem-solve and make critical decisions on trial design, vendor selection, and risk management Responsabilidades • University degree in medicine, science, or equivalent combination of education u0026 experience • Demonstrated ability to drive clinical deliverables of a study • Subject matter expertise in the designated therapeutic area • Prior monitoring experience is preferred • Willingness to travel approximately 25% Requisitos principales • Competitive base salary and performance-related incentives • Health, dental, and vision coverage • Retirement and pension plans • Life assurance and disability coverage • Employee assistance programmes and wellbeing resources • Learning and development opportunities through structured training

En nuestras residencias de Barcelona, Amavir Diagonal y Amavir Horta, precisamos incorporar enfermeras/os. Si quieres trabajar con nosotros y tienes alguna disponibilidad, no dudes en dejarnos tu CV y nos pondremos en contacto contigo lo antes posible. Se ofrece salario por encima de convenio que incluye dos pluses. AMAVIR garantiza la aplicación del principio de igualdad de oportunidades y la no discriminación en la gestión de sus procesos de reclutamiento y selección.

Nuestra residencia Amavir Diagonal necesita incorporar un/a Enfermero/a para trabajar en turno de noche en semana corta / semana larga.

ph3Experteer Overview /h3 pIn this role you will lead integrated marketing communications to drive growth for Ecolab’s high-tech business in Europe, with a focus on data centers and microelectronics. You will partner with cross‑functional teams to shape messaging, enable sales, and execute demand‑gen campaigns across digital and traditional channels. You will manage agencies, align with global and regional teams, and contribute to commercialization of new products and digital solutions. Your work will blend market insights with technical storytelling to support scalable, multi‑channel campaigns that win in complex markets. /p h3Responsibilities /h3 ul liDevelop and execute integrated marketing campaigns aligned to growth priorities /li liTranslate technical solutions into compelling value propositions and customer‑facing content /li liLead demand generation and campaign activation across digital, paid, owned, and earned channels /li liCreate sales enablement tools (presentations, case studies, solution briefs, assets) to support commercial success /li liSupport commercialization of new products, services, and digital solutions with cross‑functional partners /li liLeverage customer insights, market trends, and competitive intelligence to inform messaging and strategy /li liManage agency partners to deliver high‑quality creative and on‑time execution /li liCollaborate with global and regional teams to ensure aligned, integrated execution /li liOrganize and participate in events, media, and thought leadership activities /li /ul h3Qualifications /h3 ul liBachelor’s degree in marketing, communications, or related field /li li5+ years of marketing communications experience with integrated campaign ownership /li liExperience in data center, microelectronics, or other high‑tech/industrial markets /li liProven ability to work across a matrix organization with global and regional teams /li liStrong written and verbal communication skills, with ability to simplify technical concepts /li liExperience across digital channels (web, email, social, paid media) /li /ul h3Benefits /h3 ul liAnnual bonus /li liComprehensive benefits /li liDEI commitment /li liCompetitive compensation /li liGlobal collaboration opportunities /li liProfessional development support /li /ul pMarketing Communications Manager - Europe High Tech Division • Barcelona, Kingdom Of Spain, ES /p /p #J-18808-Ljbffr

Se busca personal para una conocida clínica de reproducción asistida en Barcelona (zona Sant Gervasi) con el objetivo de atender a pacientes italianos. Las funciones principales incluyen gestionar y acompañar a pacientes internacionales, coordinar citas y procedimientos, actualizar historiales clínicos, y mantener una comunicación constante para resolver dudas y ofrecer orientación básica sobre tratamientos y protocolos. También se apoya al equipo médico en tareas administrativas y logísticas, se colabora en el seguimiento de indicaciones, se prepara documentación, se coordinan pruebas diagnósticas y se generan facturas, todo para asegurar una atención cálida y organizada en un proceso emocionalmente delicado. Los requisitos indispensables son tener un nivel bilingüe de italiano (se realizará prueba), formación profesional en el sector sanitario, y conocimientos demostrables en reproducción asistida junto con experiencia en clínicas de fertilidad desempeñando roles similares. Se ofrece un contrato estable y directo con la empresa, salario acorde a la valía, y horario de lunes a viernes de 8 a 16 h.

Experteer Overview En Marlex, acompaña a Farmaconsulting en la transmisión patrimonial de farmacias, liderando a los clientes en el proceso y ejercitando un enfoque de alto rendimiento. Te integrarás en un equipo en expansión y competirás por nuevos clientes estratégicos, aplicando un método ganador que garantiza calidad en cada paso. Serás un referente en la zona, con oportunidades de crecimiento continuo. Esta posición combina liderazgo, experticia sectorial y impacto directo en el patrimonio farmacéutico de España. Compensaciones / Beneficios • Guiar y liderar el proceso de transmisión patrimonial de farmacias para clientes • Prospectar y captar nuevos clientes estratégicos • Gestión de las necesidades de los clientes y seguimiento de sus procesos • Aplicar el método exclusivo y probado para asegurar satisfacción y calidad • Contribuir al crecimiento del equipo y de la presencia en la zona Responsabilidades • Formación en Administración de Empresas (o afines) • +3 años de experiencia en ventas o asesoría comercial • Habilidades de comunicación, negociación y enfoque al cliente • Proactividad y pasión por el sector farmacéutico Requisitos principales • Máster propio de 7 semanas • Más de 10.000 horas anuales de aprendizaje • Contrato indefinido • Fijo anual y variable sin techo • Equipo de 75 especialistas • Estabilidad en un sector en expansión

Buscas trabajo en salud y bienestar? Este mes de julio surgen nuevas oportunidades para enfermería y medicina en Barberà del Vallès.