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Responsibilities (a) Site management • Study site selection, initiation (SIV) and clinical monitoring. • Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience. • Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and relevant regulations. • Ensure Principal Investigator/study staff complies with safety reporting requirements, as defined in protocol, SOP, ICH-GCP and GCP. • Track study recruitment to ensure recruitment target is achieved in all studies. • Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner coordinating. • Ensure timely coordination of study materials (drug, non-drug, equipments, CRFs) to the site for start-up and throughout the study. • Assemble site specific EC submission dossier, and ensure submission to EC. Training • Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol and requirements. • Conduct site initiation to ensure that the site has a thorough understanding of the study protocol and requirements. Documentation • Ensure timely collection of essential documents in compliance with protocol and regulations at study start-up, during and at study close-down. Maintain and update these documents in investigator files, trial master files. • Prepare/complete study records’ archiving according to protocol and sponsor requirements. (b) Drug Safety • Ensure safety information is disseminated to all sites according SOP and applicable regulations. • Ensure SAE is reported within the timeline in compliance with SOPs and applicable regulations. (c) Finance and Administration • Finalize budget and obtain signed contract from site, prior to site initiation visit. • Ensure Study Payment Schedule is executed and retain relevant documents/receipts. (d) Study Tools and system • Update and maintain Study tools/systems in a timely manner. 1. Qualifications 3.1 Bachelor degree or above in Medical, Pharmacology or Biology related major. 3.2 At least 8 year of CRA experience; 3.3 Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/procedures; 3.4 Good skills on Microsoft Word, Excel, PPT and Outlook, etc.

Responsibilities Cualquier información adicional que necesite para este trabajo se encuentra en el texto a continuación. Asegúrese de leerla detenidamente y luego envíe su solicitud. (a) Site management • Study site selection, initiation (SIV) and clinical monitoring., • Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience., • Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and relevant regulations., • Ensure Principal Investigator/study staff complies with safety reporting requirements, as defined in protocol, SOP, ICH-GCP and GCP., • Track study recruitment to ensure recruitment target is achieved in all studies., • Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner coordinating., • Ensure timely coordination of study materials (drug, non-drug, equipments, CRFs) to the site for start-up and throughout the study., • Assemble site specific EC submission dossier, and ensure submission to EC. Training • Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol and requirements., • Conduct site initiation to ensure that the site has a thorough understanding of the study protocol and requirements. Documentation • Ensure timely collection of essential documents in compliance with protocol and regulations at study start-up, during and at study close-down. Maintain and update these documents in investigator files, trial master files., • Prepare/complete study records’ archiving according to protocol and sponsor requirements. (b) Drug Safety • Ensure safety information is disseminated to all sites according SOP and applicable regulations., • Ensure SAE is reported within the timeline in compliance with SOPs and applicable regulations. (c) Finance and Administration • Finalize budget and obtain signed contract from site, prior to site initiation visit., • Ensure Study Payment Schedule is executed and retain relevant documents/receipts. (d) Study Tools and system • Update and maintain Study tools/systems in a timely manner. xqbhyrx 1. Qualifications 3.1 Bachelor degree or above in Medical, Pharmacology or Biology related major. 3.2 At least 8 year of CRA experience; 3.3 Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/procedures; 3.4 Good skills on Microsoft Word, Excel, PPT and Outlook, etc.

Responsibilities (a) Site management •br/br/Study site selection, initiation (SIV) and clinical monitoring. •br/br/Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience. •br/br/Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and relevant regulations. •br/br/Ensure Principal Investigator/study staff complies with safety reporting requirements, as defined in protocol, SOP, ICH-GCP and GCP. •br/br/Track study recruitment to ensure recruitment target is achieved in all studies. •br/br/Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner coordinating. •br/br/Ensure timely coordination of study materials (drug, non-drug, equipments, CRFs) to the site for start-up and throughout the study. •br/br/Assemble site specific EC submission dossier, and ensure submission to EC. Training •br/br/Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol and requirements. •br/br/Conduct site initiation to ensure that the site has a thorough understanding of the study protocol and requirements. Documentation •br/br/Ensure timely collection of essential documents in compliance with protocol and regulations at study start-up, during and at study close-down. Maintain and update these documents in investigator files, trial master files. •br/br/Prepare/complete study records’ archiving according to protocol and sponsor requirements. (b) Drug Safety •br/br/Ensure safety information is disseminated to all sites according SOP and applicable regulations. •br/br/Ensure SAE is reported within the timeline in compliance with SOPs and applicable regulations. (c) Finance and Administration •br/br/Finalize budget and obtain signed contract from site, prior to site initiation visit. •br/br/Ensure Study Payment Schedule is executed and retain relevant documents/receipts. (d) Study Tools and system •br/br/Update and maintain Study tools/systems in a timely manner.br/br/3. Qualifications 3.1 Bachelor degree or above in Medical, Pharmacology or Biology related major. 3.2 At least 8 year of CRA experience; 3.3 Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/procedures; 3.4 Good skills on Microsoft Word, Excel, PPT and Outlook, etc.

Responsibilities (a) Site management • Study site selection, initiation (SIV) and clinical monitoring., • Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience., • Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and relevant regulations., • Ensure Principal Investigator/study staff complies with safety reporting requirements, as defined in protocol, SOP, ICH-GCP and GCP., • Track study recruitment to ensure recruitment target is achieved in all studies., • Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner coordinating., • Ensure timely coordination of study materials (drug, non-drug, equipments, CRFs) to the site for start-up and throughout the study., • Assemble site specific EC submission dossier, and ensure submission to EC. Training • Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol and requirements., • Conduct site initiation to ensure that the site has a thorough understanding of the study protocol and requirements. Documentation • Ensure timely collection of essential documents in compliance with protocol and regulations at study start-up, during and at study close-down. Maintain and update these documents in investigator files, trial master files., • Prepare/complete study records’ archiving according to protocol and sponsor requirements. (b) Drug Safety • Ensure safety information is disseminated to all sites according SOP and applicable regulations., • Ensure SAE is reported within the timeline in compliance with SOPs and applicable regulations. (c) Finance and Administration • Finalize budget and obtain signed contract from site, prior to site initiation visit., • Ensure Study Payment Schedule is executed and retain relevant documents/receipts. (d) Study Tools and system • Update and maintain Study tools/systems in a timely manner. 1. Qualifications 3.1 Bachelor degree or above in Medical, Pharmacology or Biology related major. 3.2 At least 8 year of CRA experience; 3.3 Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/procedures; 3.4 Good skills on Microsoft Word, Excel, PPT and Outlook, etc.

Responsibilities Cualquier información adicional que necesite para este trabajo se encuentra en el texto a continuación. Asegúrese de leerla detenidamente y luego envíe su solicitud. (a) Site management • Study site selection, initiation (SIV) and clinical monitoring., • Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience., • Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and relevant regulations., • Ensure Principal Investigator/study staff complies with safety reporting requirements, as defined in protocol, SOP, ICH-GCP and GCP., • Track study recruitment to ensure recruitment target is achieved in all studies., • Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner coordinating., • Ensure timely coordination of study materials (drug, non-drug, equipments, CRFs) to the site for start-up and throughout the study., • Assemble site specific EC submission dossier, and ensure submission to EC. Training • Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol and requirements., • Conduct site initiation to ensure that the site has a thorough understanding of the study protocol and requirements. Documentation • Ensure timely collection of essential documents in compliance with protocol and regulations at study start-up, during and at study close-down. Maintain and update these documents in investigator files, trial master files., • Prepare/complete study records’ archiving according to protocol and sponsor requirements. (b) Drug Safety • Ensure safety information is disseminated to all sites according SOP and applicable regulations., • Ensure SAE is reported within the timeline in compliance with SOPs and applicable regulations. (c) Finance and Administration • Finalize budget and obtain signed contract from site, prior to site initiation visit., • Ensure Study Payment Schedule is executed and retain relevant documents/receipts. (d) Study Tools and system • Update and maintain Study tools/systems in a timely manner. xqbhyrx 1. Qualifications 3.1 Bachelor degree or above in Medical, Pharmacology or Biology related major. 3.2 At least 8 year of CRA experience; 3.3 Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/procedures; 3.4 Good skills on Microsoft Word, Excel, PPT and Outlook, etc.

ph3Responsibilities /h3ulliEnsure consistent processes and efficient review of critical clinical/safety data /liliReview of patient-level clinical/safety data on an ongoing basis to ensure medical accuracy and completeness, coding consistency and generate applicable queries as needed to obtain information for appropriate medical assessment and case closure /liliPrepare aggregated data visualization and facilitate meetings related to review of safety data on study level /liliContribute to study start-up activities according to the applicable process/procedures (ex. input to the applicable documents, tools set up) /liliServe as a member of the Extended Study Team and report on TRISARC deliverables /liliWork with the study physicians and/or clinical/project scientists to support standardized high-level data review and medical evaluation /liliEscalate urgent and critical medical cases to the study physician/medical scientist as appropriate /liliProvide input into the process of setting automated patient narratives, if applicable /liliProvide input to establishing the process for handwritten patient narratives, including guideline development and the quality control process if applicable /liliLead quality of own deliverables /liliTake on tasks as assigned by the Directors, Associate Directors Clinical Trial Safety /liliProvide input into non-drug project work including training activities, continuous improvement and development of procedures as needed /li /ulh3Education/Experience /h3ulliEducational degree (BSc/Msc/PhD) in Life Science or equivalent work experience in directly related fields /liliMinimum 2+ years of experience in Pharmacovigilance / Drug Safety /liliUnderstanding of the clinical study and drug development process /liliKnowledge of ICH/GCP Guidelines /liliKnowledge of SAE reporting requirements /liliExperience using data review tools is preferred /liliQuality focus, analytical skills, and ability to concisely summarize large amounts of complex information /liliProven ability to prioritize and manage multiple tasks with conflicting deadlines /liliExcellent time management /liliVery good interpersonal and communication skills /liliTeam player, able to work individually /liliAbility and willingness to work cross-functionally, e.g. with internal and external partners, on global studies, across different phases of drug development or different therapy areas /li /ulpIQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at /ppIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. /ppAt IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies. /p /p #J-18808-Ljbffr

Experteer Overview Las cualificaciones, habilidades y toda la experiencia relevante necesaria para este puesto se pueden encontrar en la descripción completa a continuación. In this role you provide medical, clinical, and scientific advisory support across IQVIA divisions and trial projects. You act as a medical expert throughout the project lifecycle and contribute to business development with medically grounded insights. You lead medical monitoring and strategic input to ensure protocol and safety quality. This position blends hands-on medical oversight with cross-functional collaboration to advance trial delivery and science-driven proposals. Compensaciones / Beneficios • Serve as Global and/or Regional Medical Advisor on assigned projects and provide guidance to project leaders on medical and scientific aspects, • Support investigative sites and project staff on protocol clarifications, eligibility, and patient safety, • Review protocols, IDB, and CRFs for medical accuracy and safety considerations, • Provide therapeutic area/trial training to the clinical team and participate in Investigator Meetings, • Review and clarify adverse events (AEs) and potentially handle SAE case reviews with Pharmacovigilance, • Support AOSE analysis and adverse event coding review as needed, • Review CSR and patient narratives; participate in kick-off and regular team/client meetings, • Be available 24/7 to respond to urgent protocol-related questions from sites, • Contribute to medical strategy for multi-region studies and client proposals, including medical budget, • Present at bid defense meetings and engage in strategic BD activities; stay updated on industry developments, • Travel regionally and internationally as required, • Maintain relationships with coworkers, managers, and clients with strong communication and presentation skills Responsabilidades • Medical degree from an accredited medical school with relevant medical education, • Specialty board certification xqbhyrx in Neurology, • Ideally 2 years clinical trials experience as investigator or medical/clinical expert in pharma/CRO/biotech, • Strong communication, presentation, and interpersonal skills in English, • Robust knowledge of scientific, clinical, regulatory, and competitive landscape in the therapeutic area, • Ability to work independently and collaboratively in cross-functional settings, • Proven ability to provide consultation across multiple assignments with initiative and flexibility, • Experience in establishing working relationships with colleagues and clients Requisitos principales

ppbLocation: /b Madrid, Spain /p pbWork Regime: /b Full-time | Hybrid/remote /p h3Responsibilities and Tasks /h3 ul liSupport the definition, development and implementation of cybersecurity requirements for automotive systems and components, ensuring compliance with applicable standards and regulations. /li liEnsure the application of ISO/SAE 21434 throughout the relevant phases of the automotive product development lifecycle. /li liPerform and support cybersecurity risk assessment activities, including Threat Analysis and Risk Assessment (TARA), identifying potential threats, attack paths and associated risks. /li liContribute to the definition and development of cybersecurity concepts, goals and requirements, ensuring their correct implementation and traceability throughout the project lifecycle. /li liAct as a technical interface between Product Compliance, systems, software, hardware and engineering teams, translating cybersecurity and regulatory requirements into clear and actionable technical specifications. /li liReview system architectures, technical specifications and engineering deliverables from a cybersecurity perspective, identifying potential vulnerabilities and areas of non-compliance. /li liSupport the definition and follow-up of cybersecurity mitigation measures and contribute to the resolution of complex cybersecurity-related technical issues. /li liParticipate in technical reviews, cybersecurity assessments and compliance activities, ensuring that project deliverables meet the applicable cybersecurity requirements. /li liCollaborate closely with cross-functional engineering teams and relevant stakeholders to ensure the consistent integration of cybersecurity requirements into automotive systems and products. /li liSupport the preparation and maintenance of cybersecurity-related technical documentation and evidence required for compliance and assessment activities. /li /ul h3Mandatory Requirements /h3 ul liDegree in Automotive, Electrical, Electronics, Computer, Telecommunications Engineering or a similar technical field. /li liAt least 5 years of professional experience in the automotive industry. /li liProfessional experience in automotive cybersecurity or cybersecurity engineering applied to embedded automotive systems. /li liStrong knowledge of ISO/SAE 21434 and automotive cybersecurity engineering principles. /li liExperience with cybersecurity risk assessment methodologies, particularly Threat Analysis and Risk Assessment (TARA). /li liGood understanding of automotive electrical/electronic architectures, embedded systems and software development processes. /li liAbility to analyse complex systems and translate cybersecurity and regulatory requirements into actionable engineering requirements. /li liStrong analytical and problem-solving skills. /li liGood command of English, both written and spoken. /li /ul h3Complementary Requirements /h3 ul liKnowledge of UNECE R155 and automotive Cybersecurity Management Systems (CSMS) is considered a strong advantage. /li liKnowledge of UNECE R156 and Software Update Management Systems (SUMS) is a plus. /li liExperience with cybersecurity concepts, cybersecurity requirements, cybersecurity case development and compliance evidence is an advantage. /li liKnowledge of ISO 26262 and automotive Functional Safety is considered a plus. /li liKnowledge of ASPICE and AUTOSAR is considered a plus. /li liExperience with hybrid or electrified powertrains and their electronic architectures is an advantage. /li liKnowledge of French is considered a plus. /li /ul h3Benefits /h3 h3Important /h3 ul liOur company does not sponsor work visas or work permits. All applicants must have the legal right to work in the country where the position is based. /li liOnly candidates who meet the required qualifications and match the profile requested by our clients will be contacted. /li /ul p#VisionaryFuture - Build the future, join our living ecosystem! /p /p #J-18808-Ljbffr

Indra Group, líder en tecnología y consultoría, busca un Responsable Técnico de Producto – Plataforma SAE para coordinar equipos multidisciplinares en un entorno internacional. Consulte la descripción del puesto a continuación. Si confía en que tiene las habilidades y la experiencia adecuadas, envíe su solicitud hoy mismo. Se valorará experiencia en transporte y movilidad, integración de sistemas y diseño técnico de soluciones. Ofrecemos estabilidad, proyectos de gran alcance y formación continua, junto a un entorno transparente y colaborativo en Indra Mobility. xqbhyrx Inglés alto y disponibilidad para trabajar en España. #J-18808-Ljbffr

En Indra Group, protegemos lo que más importa. Somos una multinacional española de tecnología y consultoría que desarrolla sistemas y servicios avanzados en sectores clave como Defensa, Espacio, Movilidad y Tráfico Aéreo, con presencia internacional y proyectos de alto impacto tecnológico. ¿Posee las habilidades y la experiencia adecuadas para este puesto? Siga leyendo para descubrirlo y envíe su solicitud. Trabaja con nosotros en Indra Mobility! Nuestra división especializada en ofrecer soluciones tecnológicas innovadoras para el sector del transporte y la movilidad, desarrollando sistemas críticos de ticketing, control de acceso y gestión de pagos que utilizan millones de personas cada día en todo el mundo. En Indra, buscamos incorporar un/a Responsable Técnico de Producto – Plataforma SAE para participar coordinando equipos multidisciplinares en un entorno internacional. Responsabilidades principales • Ser responsable técnico de producto y plataforma SAE, colaborando en el diseño técnico y evolución de soluciones., • Coordinar equipos de desarrollo en proyectos del sector transporte., • Participar en el análisis funcional, implantación y puesta en marcha de soluciones con cliente., • Colaborar en el diseño técnico del producto y su evolución., • Aportar soporte técnico en la preparación de ofertas., • Asegurar la correcta integración de sistemas (planificadores, optimizadores, software de explotación)., • Interactuar con clientes para garantizar el éxito de las soluciones implantadas. No te preocupes si no cumples el 100% de lo que buscamos. ¡Anímate, conoce nuestra propuesta y así conoceremos lo que nos puedes aportar! Requisitos • Titulación en Telecomunicaciones o Informática., • Experiencia como responsable técnico o líder técnico en proyectos de transporte o movilidad, gestionando equipos de desarrollo (más de 4 años)., • Conocimiento en entornos SAE (Sistemas de Ayuda a la Explotación)., • Experiencia en análisis funcional, implantación y puesta en marcha., • Conocimiento en diseño técnico de soluciones y colaboración en ofertas., • Conocimientos en consultoría cloud, Java, XML, integración de aplicaciones, servicios web, Spring DI, orientación a objetos y arquitectura de microservicios., • Experiencia en movilidad: equipamiento embarcado, paneles informativos TFT, SAEs, integración de planificadores/optimizadores, software de gestión y planes de explotación., • Conocimiento en herramientas de gestión de proyectos (Project, Jira)., • Conocimiento en software de gestión y planes de explotación en movilidad., • Experiencia en integración con planificadores/optimizadores., • Nivel alto de inglés, hablado y escrito. Lo que te ofrecemos • Estabilidad y Futuro: Proyectos a largo plazo en una empresa líder con más de 60.000 profesionales, con seguridad financiera., • Proyectos Innovadores y de Alto Alcance: Trabajarás con tecnologías de vanguardia, con un impacto tanto a nivel nacional como internacional., • Ambiente Cercano y Transparente: Disfrutarás de una comunicación directa y fluida con responsables y compañeros, en un entorno colaborativo y abierto., • Autonomía y Flexibilidad: Tendrás libertad para organizar tu trabajo, con una conciliación real y adaptada a tu ritmo., • Plan de carrera adaptado a ti: Diseñado para impulsar tu crecimiento y desarrollo profesional., • Formación continua: en Open University y Udemy for Business (más de 6.000 cursos para especializarte!)., • Descuentos exclusivos para tu bienestar: Disfruta de ventajas en gimnasios, restaurantes, tiendas, ocio y mucho más al ser empleado de Indra., • Retribución competitiva y planes de compensación flexibles a tus necesidades. ¿Cómo es nuestro proceso de selección? • Revisión de tu perfil: Evaluamos tu experiencia y habilidades para determinar si encajas con lo que buscamos., • Primera toma de contacto (5-10 min): Si recibes una llamada de un número desconocido, será una conversación rápida para conocerte y resolver cualquier duda., • Entrevista técnica: Te reunirás con el equipo, quienes te explicarán el proyecto y las tareas diarias. También exploraremos tus conocimientos técnicos. Además, te realizaremos breves pruebas de competencias psicológicas e inglés (si es necesario)., • Entrevista con el equipo de atracción de talento: Queremos que nos conozcas mejor como empresa: valores, modelo de carrera, skills… para que tanto tú como el equipo podáis analizar si hay match., • Oferta y bienvenida: Si todo va bien, te incorporas a nuestro equipo y comenzamos esta nueva etapa juntos. ¿Listo para formar parte de un equipo que transforma el futuro de la movilidad? Nosu compromiso es promover ambientes de trabajo en los que se trate con respeto y dignidad a las personas, procurando el desarrollo profesional de la plantilla y garantizando la igualdad de oportunidades en su selección, formación y promoción ofreciendo un entorno de trabajo libre de cualquier discriminación por motivo de género, edad, discapacidad, orientación sexual, identidad o expresión de género, religión, etnia, estado civil o cualquier otra circunstancia personal o social. xcskxlj ¡INDRA es empresa Top Employer 2026! Incorpórate a una de las mejores empresas empleadoras de España, reconocida por su gestión integral de RRHH y el cuidado de sus profesionales. #J-18808-Ljbffr

pulliSupport the definition, development and implementation of Functional Safety requirements for automotive systems and components, ensuring compliance with ISO 26262 and applicable automotive safety requirements. /liliContribute to Functional Safety activities throughout the relevant phases of the automotive product development lifecycle, from concept definition to system, hardware and software development. /liliPerform and support Hazard Analysis and Risk Assessment (HARA) activities, including hazard identification, risk classification and Automotive Safety Integrity Level (ASIL) determination. /liliContribute to the definition and development of Safety Goals, Functional Safety Concepts and Technical Safety Concepts. /liliDefine, analyse and follow up Functional Safety requirements, ensuring their correct allocation, implementation, verification and traceability throughout the project lifecycle. /liliAct as a technical interface between Product Compliance, systems, software, hardware and engineering teams, translating Functional Safety requirements into clear and actionable technical specifications. /liliReview system architectures, technical specifications and engineering deliverables to ensure compliance with Functional Safety requirements and ISO 26262. /liliSupport safety analyses and the identification and resolution of complex safety-related issues in automotive systems. /liliParticipate in technical reviews, safety assessments and compliance activities, ensuring that the required Functional Safety deliverables and evidence are available and compliant. /liliCollaborate closely with cross-functional engineering teams to ensure the consistent integration of Functional Safety requirements across system, hardware and software development. /liliSupport the preparation and maintenance of Functional Safety documentation and safety-related work products throughout the project lifecycle. /li /ulpbLocation: /b Madrid, Spain /ppbWork Regime: /b Full-time | Hybrid/remote /ph3Responsibilities and Tasks /h3ulliSupport the definition, development and implementation of Functional Safety requirements for automotive systems and components, ensuring compliance with ISO 26262 and applicable automotive safety requirements. /liliContribute to Functional Safety activities throughout the relevant phases of the automotive product development lifecycle, from concept definition to system, hardware and software development. /liliPerform and support Hazard Analysis and Risk Assessment (HARA) activities, including hazard identification, risk classification and Automotive Safety Integrity Level (ASIL) determination. /liliContribute to the definition and development of Safety Goals, Functional Safety Concepts and Technical Safety Concepts. /liliDefine, analyse and follow up Functional Safety requirements, ensuring their correct allocation, implementation, verification and traceability throughout the project lifecycle. /liliAct as a technical interface between Product Compliance, systems, software, hardware and engineering teams, translating Functional Safety requirements into clear and actionable technical specifications. /liliReview system architectures, technical specifications and engineering deliverables to ensure compliance with Functional Safety requirements and ISO 26262. /liliSupport safety analyses and the identification and resolution of complex safety-related issues in automotive systems. /liliParticipate in technical reviews, safety assessments and compliance activities, ensuring that the required Functional Safety deliverables and evidence are available and compliant. /liliCollaborate closely with cross-functional engineering teams to ensure the consistent integration of Functional Safety requirements across system, hardware and software development. /liliSupport the preparation and maintenance of Functional Safety documentation and safety-related work products throughout the project lifecycle. /li /ulh3Mandatory Requirements /h3ulliDegree in Automotive, Electrical, Electronics, Mechanical Engineering or a similar technical field. /liliAt least 5 years of professional experience in the automotive industry. /liliProfessional experience in Functional Safety applied to automotive systems. /liliStrong knowledge of ISO 26262 and its application throughout the automotive product development lifecycle. /liliExperience with Hazard Analysis and Risk Assessment (HARA), Safety Goals and ASIL classification. /liliKnowledge of Functional Safety Concept and Technical Safety Concept development. /liliGood understanding of automotive electrical/electronic architectures, embedded systems and system development processes. /liliAbility to analyse complex systems and translate safety and regulatory requirements into actionable engineering requirements. /liliStrong analytical and problem-solving skills. /liliGood command of English, both written and spoken. /li /ulh3Complementary Requirements /h3ulliExperience with Functional Safety requirements management, traceability and verification activities is considered an advantage. /liliExperience with safety analyses such as FMEA, FTA or similar methodologies is a plus. /liliKnowledge of automotive powertrain systems, hybrid or electrified vehicles and their critical electronic components is an advantage. /liliKnowledge of ISO/SAE 21434 and automotive cybersecurity is considered a plus. /liliKnowledge of ASPICE and AUTOSAR is considered a plus. /liliExperience working with multidisciplinary system, software and hardware engineering teams is an advantage. /liliKnowledge of French is considered a plus. /li /ulh3Benefits /h3ulliOur company does not sponsor work visas or work permits. All applicants must have the legal right to work in the country where the position is based. /liliOnly candidates who meet the required qualifications and match the profile requested by our clients will be contacted. /li /ulh3Important /h3ulliOur company does not sponsor work visas or work permits. All applicants must have the legal right to work in the country where the position is based. /liliOnly candidates who meet the required qualifications and match the profile requested by our clients will be contacted. /li /ulp#VisionaryFuture - Build the future, join our living ecosystem! /p /p #J-18808-Ljbffr

pResponsibilities /pp(a) Site management /pp• Study site selection, initiation (SIV) and clinical monitoring. Las cualificaciones, habilidades y toda la experiencia relevante necesaria para este puesto se pueden encontrar en la descripción completa a continuación. /pp• Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience. /pp• Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and relevant regulations. /pp• Ensure Principal Investigator/study staff complies with safety reporting requirements, as defined in protocol, SOP, ICH-GCP and GCP. /pp• Track study recruitment to ensure recruitment target is achieved in all studies. /pp• Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner coordinating. /pp• Ensure timely coordination of study materials (drug, non-drug, equipments, CRFs) to the site for start-up and throughout the study. /pp• Assemble site specific EC submission dossier, and ensure submission to EC. /ppTraining /pp• Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol and requirements. /pp• Conduct site initiation to ensure that the site has a thorough understanding of the study protocol and requirements. /ppDocumentation /pp• Ensure timely collection of essential documents in compliance with protocol and regulations at study start-up, during and at study close-down. Maintain and update these documents in investigator files, trial master files. /pp• Prepare/complete study records’ archiving according to protocol and sponsor requirements. /pp(b) Drug Safety /pp• Ensure safety information is disseminated to all sites according SOP and applicable regulations. /pp• Ensure SAE is reported within the timeline in compliance with SOPs and applicable regulations. /pp(c) Finance and Administration /pp• Finalize budget and obtain signed contract from site, prior to site initiation visit. /pp• Ensure Study Payment Schedule is executed and retain relevant documents/receipts. /pp(d) Study Tools and system /pp• Update and maintain Study tools/systems in a timely manner. xqbhyrx /p p3. Qualifications /pp3.1 Bachelor degree or above in Medical, Pharmacology or Biology related major. /pp3.2 At least 8 year of CRA experience; /pp3.3 Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/procedures; /pp3.4 Good skills on Microsoft Word, Excel, PPT and Outlook, etc. /p

pVectalia, grupo líder en servicios de transporte y movilidad, busca un/a Técnico/a de Planificación de Redes de Transporte para diseñar y desarrollar la parte gráfica de proyectos del área de transporte colectivo. Se trabajará con planos, GIS, y extracción de datos del SAE y de sistemas de ticketing. /ppSe valorará experiencia en herramientas de diseño gráfico (Illustrator, InDesign, Photoshop) y en Python/R para automatización. Contrato indefinido a jornada completa con horario flexible. /p #J-18808-Ljbffr

Como parte del Equipo de Ingeniería Eléctrica, participarás conjuntamente en el desarrollo de soluciones técnicas certificables a través de la realización de planos, documentos de ingeniería, informes y pruebas; brindando también soporte de ingeniería general bajo supervisión directa. Colaborará estrechamente con clientes internos de ingeniería, fabricación e instalación, ascendentes y descendentes, para garantizar que la producción esté alineada globalmente y se ejecute de manera efectiva. ¿Está pensando en solicitar este empleo? No se demore, desplácese hacia abajo y envíe su solicitud lo antes posible para no perder la oportunidad. Importante: solo aplicaciones en inglés serán tomadas en cuenta. Responsabilidades • Preparar planos y documentos de ingeniería que cumplan con todos los requisitos reconocidos de seguridad, certificación y del cliente bajo supervisión directa., • Revisar la configuración eléctrica de la aeronave para verificar la viabilidad, precisión e integridad del alcance del trabajo., • Realizar y analizar cálculos eléctricos (por ejemplo, análisis de carga, definición de protección o selección de cableado)., • Brindar información al ingeniero principal para completar un plan de publicación de planos para una tarea/proyecto específico., • Participar y/o presenciar pruebas y preparar los informes correspondientes según sea necesario., • Brindar información al ingeniero principal sobre el estado del proyecto., • Identificar cualquier desviación del proceso, así como oportunidades de reducción de costos en referencia al proyecto., • Participar en iniciativas de mejora continua, para simplificar el proceso y el trabajo de valor agregado.Requisitos, • Grado/licenciatura en electricidad o graduado/licenciado en aeronáutica con experiencia en electricidad)., • 5 años de experiencia en ingeniería eléctrica., • Conocimiento general de la normativa aeronáutica (EASA y/o FAA) y del proceso de desarrollo de documentación., • Fluidez en inglés y español (escrito y hablado)., • Conocimiento de diseño en Autocad Electrical es un plus., • Certificado técnico y/o experiencia práctica relevante en un entorno de producción, instalación o ingeniería en el sector aeroespacial., • Deseable tener conocimientos en conceptos de generación de energía, distribución eléctrica y/o arquitecturas de aire acondicionado., • Definición de cableado/cableado (es deseable tener conocimientos de EWIS), • Conocimientos normativos de aeronaves (p. ej., ambientales: RTCA DO-160 y MIL-STD-810, eléctricos: MIL-STD-704810, análisis de carga: MIL-E-7016, cableado: MIL-STD-5088 o SAE AS 50881, etc.)Beneficios, • Formar parte de un grupo internacional consolidado., • Proyecto de futuro, con oportunidades reales de crecimiento., • Buen ambiente de trabajo en entorno colaborativo y proactivo., • Salario competitivo, acorde al mercado y a tu experiencia., • Ticket restaurante., • Modelo de trabajo híbrido. xqbhyrx, • Seguro médico. #J-18808-Ljbffr

Únete a NTT DATA y diseña la movilidad inteligente del futuro Es posible que un gran número de candidatos se presenten a este puesto, así que asegúrese de enviar su CV y su solicitud lo antes posible. En NTT DATA somos más de 190.000 profesionales en más de 50 países, unidos por una misma ambición: utilizar la tecnología para transformar la sociedad de forma sostenible, eficiente y centrada en las personas. Trabajamos en sectores clave —energía, industria, telecomunicaciones, banca, sector público, sanidad impulsando soluciones innovadoras que generan impacto real. Green Deal & Sustainability | Transporte Público y Movilidad: En el equipo de Movilidad Sostenible lideramos la transformación digital del transporte público y la movilidad urbana. Diseñamos soluciones avanzadas que conectan tecnología, datos y experiencia de usuario para construir ciudades más inteligentes, accesibles y sostenibles. Para seguir creciendo, buscamos perfiles analíticos con visión de negocio, conocimiento funcional y pasión por la movilidad. • Analistas Funcionales / Analistas IT con experiencia o conocimiento en transporte público y movilidad, que quieran participar en el diseño de soluciones complejas, innovadoras y de alto impacto social., • Conocimiento o experiencia en ecosistemas de movilidad: MaaS, planificadores de ruta, sistemas de información y estándares de transporte., • Experiencia con estándares y modelos como Transmodel, GTFS, GTFS-RT, TRIAS, HAFAS, TAP-TSI, entre otros., • Interés o experiencia en sistemas de pago e información en transporte público (ABT, EMV, contactless, SAE, MaaS…)., • Capacidad para entender el viaje completo del usuario (búsqueda, reserva, viaje, cambios, devoluciones, alertas…)., • Conocimiento de tapping, Pay-as-you-go, virtualización de tarjetas, NFC y tokens (QR, Aztec, códigos de barras)., • Experiencia o familiaridad con arquitecturas de integración, colas de mensajería, sistemas síncronos y asíncronos, ESB., • Mentalidad analítica, curiosidad técnica y orientación a la mejora continua. ¿Cuál será tu rol en el equipo? • Actuar como puente entre negocio y tecnología, aportando conocimiento experto del sector transporte., • Definir y documentar diseños funcionales (alto, medio y bajo nivel)., • Acompañar al equipo de desarrollo, ayudándole a comprender las particularidades del dominio de movilidad., • Anticipar riesgos y proponer soluciones funcionales y técnicas., • Participar en estimaciones de esfuerzo y económicas., • Colaborar con áreas de ofertas y marketing, aportando visión de mercado., • Diseñar componentes funcionales reutilizables y parametrizables., • Investigar, innovar y proponer mejoras continuas en productos y soluciones., • Autogestionar y hacer seguimiento de los desarrollos., • Incorporarte a una comunidad de profesionales altamente cualificados, referentes en movilidad y tecnología., • Plan de carrera personalizado, donde tu crecimiento profesional es una realidad, no una promesa., • Formación continua desde el primer día (tecnología, arquitectura, dominio funcional, certificaciones)., • Programa de mentoring, con acompañamiento real en tu evolución., • Beneficios sociales (seguro médico, seguro de vida y retribución flexible)., • Modelo híbrido, flexibilidad horaria, jornada intensiva los viernes y en verano., • Excelente ambiente de trabajo, reconocido como Top Employer, donde el compañerismo y la colaboración son parte del ADN. Creemos que la diversidad impulsa la innovación. Cada persona aporta algo único, y aquí tendrás espacio para desarrollar tu singularidad, aprender continuamente y generar impacto real. xqbhyrx ¿Te animas a diseñar la movilidad del mañana con nosotros? #J-18808-Ljbffr

Responsibilities Cualquier información adicional que necesite para este trabajo se encuentra en el texto a continuación. Asegúrese de leerla detenidamente y luego envíe su solicitud. (a) Site management • Study site selection, initiation (SIV) and clinical monitoring., • Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience., • Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and relevant regulations., • Ensure Principal Investigator/study staff complies with safety reporting requirements, as defined in protocol, SOP, ICH-GCP and GCP., • Track study recruitment to ensure recruitment target is achieved in all studies., • Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner coordinating., • Ensure timely coordination of study materials (drug, non-drug, equipments, CRFs) to the site for start-up and throughout the study., • Assemble site specific EC submission dossier, and ensure submission to EC. Training • Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol and requirements., • Conduct site initiation to ensure that the site has a thorough understanding of the study protocol and requirements. Documentation • Ensure timely collection of essential documents in compliance with protocol and regulations at study start-up, during and at study close-down. Maintain and update these documents in investigator files, trial master files., • Prepare/complete study records’ archiving according to protocol and sponsor requirements. (b) Drug Safety • Ensure safety information is disseminated to all sites according SOP and applicable regulations., • Ensure SAE is reported within the timeline in compliance with SOPs and applicable regulations. (c) Finance and Administration • Finalize budget and obtain signed contract from site, prior to site initiation visit., • Ensure Study Payment Schedule is executed and retain relevant documents/receipts. (d) Study Tools and system • Update and maintain Study tools/systems in a timely manner. xqbhyrx 1. Qualifications 3.1 Bachelor degree or above in Medical, Pharmacology or Biology related major. 3.2 At least 8 year of CRA experience; 3.3 Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/procedures; 3.4 Good skills on Microsoft Word, Excel, PPT and Outlook, etc.

ppVectalia es un Grupo Empresarial con más de cien años de experiencia, consolidándose como un referente a nivel nacional en la prestación de servicios, transporte y movilidad. /p pSomos una empresa, comprometidos plenamente con la Igualdad de Oportunidades. Creemos firmemente en el talento singular de cada individuo y reconocemos que la diversidad enriquece los equipos, promoviendo organizaciones más innovadoras, creativas y eficientes. /p pBuscamos incorporar un/a bTécnico/a de Planificación de Redes de Transporte /bpara nuestro equipo de ofertas y licitaciones, que tendrá como objetivo diseñar y desarrollar la parte gráfica de los proyectos de la compañía englobados en el área de transporte colectivo de viajeros. /p h3¿Cuáles serán tus funciones? /h3 ol liDiseñar y actualizar de planos de red (urbanos e interurbanos): líneas, paradas, frecuencias, zonas tarifarias. /li liElaborar de termómetros de líneas y esquemas de recorrido para paneles informativos, marquesinas, vehículos y web/app. /li liExtraer, tratar y depurar datos procedentes del SAE (Sistema de Ayuda a la Explotación) y del sistema de ticketing (validaciones, títulos de transporte, zonificación tarifaria). Integración de datos externos (callejeros, ortofotos, capas municipales, OpenStreetMap, catastro, etc.) en entornos GIS. /li liGeorreferenciación de paradas, recorridos, carriles bus e infraestructuras de la red. /li liElaborar planos técnicos de parkings y zonas de estacionamiento regulado. /li liRealizar el mantenimiento de una base de datos geoespacial de la red (paradas, líneas, horarios, tarifas) coherente y actualizada. /li liGenerar material gráfico para paneles de información en tiempo real, señalética de parada, folletos, web y app de movilidad. /li liColaborar con los departamentos de Explotación, Sistemas/IT, Marketing y Atención al Cliente para garantizar la coherencia de la información publicada. /li liAdaptar la cartografía a criterios de accesibilidad y diseño universal (contraste, legibilidad, iconografía normalizada). /li liControlar las versiones y archivo de los distintos formatos de planos. /li /ol ul liPersona con grado/clico superior en en diseño gráfico, Cartografía y Geodesia, geografía, Ingeniería Geomática/Topografía o similar. /li liExperiencia mínima de 3-4 años en posiciones similares. /li liValorable formación específica en sistemas GIS. /li liExperiencia con herramientas de diseño gráfico:: Adobe Illustrator, InDesign, photoshop. /li liConocimientos de base de datos y hojas de cálculo (SQL, Excel). /li liValorable experiencia con formatos y estándares de datos de transporte (GTFS, GTFS-Realtime), en sistemas SAE y lenguaje de tratamiento de datos (Python, R) para automatización de procesos. /li libContratación indefinida a jornada completa. /b /li liBuen ambiente de trabajo y apoyo continuo del equipo. Jornada laboral con flexibilidad de hora de entrada y de salida en horario de lunes a jueves con horario de 8h a 17:30h y los viernes de 8h a 15h. Del 15 de junio al 15 de septiembre de 8h a 15h. /li liDesarrollo profesional en una empresa referente en su sector. /li /ul /p #J-18808-Ljbffr

You will ensure ISO/SAE 21434 compliance across product development phases and perform risk assessments including TARA.

You will ensure ISO/SAE 21434 compliance across product development phases and perform risk assessments including TARA.

Kapres Technology está buscando un Especialista en Cumplimiento Normativo para el sector automotriz.Se valorará experiencia en cumplimiento normativo, seguridad de la información y auditorías en entornos técnicos.El puesto ofrece contrato indefinido y un modelo de trabajo híbrido con dos días