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Amaris is looking for a Data Manager with strong experience in clinical data management for CRO environments. The position focuses on supervising data management activities to ensure the smooth progress and quality of clinical projects. 🔥 Your Responsibilities • Act as the main point of contact for all data management topics and participate in project/study meetings, • Contribute to the selection of subcontractors by preparing specifications and evaluating proposals, • Participate in study design, including data management sections in protocols and CRF specifications, • Oversee outsourced data management activities, ensuring compliance with cost, timelines, and data quality, • Validate deliverables such as data management plans, validation plans, transfer specifications, eCRF completion guides, and coding instructions, • Test eCRF before production deployment and after each protocol amendment, • Implement targeted quality control of data based on risk assessment, • Monitor progress of data management steps (entry, cleaning, coding, external data transfers, SAE reconciliation, etc.), • Approve SDTM specifications and verify SDTM packages as needed, • Regularly assess subcontractor service quality, establish action plans for deviations, and discuss corrective measures, • Participate in data review meetings and validate associated reports, • Ensure responsibility for database lock and unlock, verifying all prerequisites, • Provide statisticians with data for statistical analysis, • Verify the presence of all data management documentation in the Trial Master File (TMF) 🎯 Your Qualifications • Experience in clinical data management for CROs (5–10 years), • Proficiency with industry-standard data management tools and software, • Academic background in Life Sciences, Pharmacy, or related field, • English fluent. French is a plus., • You demonstrate strong analytical and problem-solving skills, • You demonstrate excellent communication skills 💡 What You’ll Get From Us • An international community bringing together 110+ different nationalities, • An environment where trust has a central place: 70% of our key leaders started their careers at the first level of responsibilities, • A robust training system with our internal Academy and 250+ available modules, • A vibrant workplace that frequently gathers for internal events (afterworks, team buildings, etc.), • At Mantu, sustainability is part of everything we do. You’ll have the opportunity to turn your ideas into action and make a tangible impact. Every day, our teams bring our ESG commitments to life, from reducing our footprint to driving positive change within our communities. Through our WeCare Together program, you’ll be empowered to design and lead projects that create real social or environmental impact, with the company’s full support. Amaris Consulting is proud to be an equal-opportunity workplace. We are committed to promoting diversity within the workforce and creating an inclusive working environment. For this purpose, we welcome applications from all qualified candidates regardless of gender, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics.

🚦 Únete a NTT DATA y lidera la movilidad del futuro En NTT DATA somos más de 190.000 profesionales en más de 50 países, conectados por una visión común: utilizar la tecnología para transformar la sociedad de forma sostenible, eficiente y responsable. Trabajamos en múltiples sectores —energía, industria, telecomunicaciones, banca, sector público, sanidad siempre desde la colaboración, la innovación y una mirada a largo plazo. 🌱 Green Deal & Sustainability | Movilidad Sostenible: Desde el equipo de Movilidad Sostenible, lideramos proyectos clave para la transformación del transporte público y la movilidad urbana. Acompañamos a administraciones y operadores en la digitalización del transporte, la implantación de sistemas inteligentes, y la evolución hacia modelos de movilidad más sostenibles, conectados y centrados en las personas. Buscamos perfiles con visión, liderazgo y experiencia, capaces de convertir la complejidad en impacto real. 💡 Buscamos: • Jefes/as de Proyecto – Project Managers IT con experiencia en movilidad, transporte y tecnología, que quieran liderar proyectos estratégicos y de gran escala, guiando a clientes públicos en su proceso de transformación digital. 🧩 ¿Qué nos gustaría que aportaras? • Experiencia demostrable gestionando grandes proyectos tecnológicos y de software, preferiblemente con clientes del sector público., • Experiencia en proyectos de transporte público y movilidad., • Conocimiento del ecosistema de movilidad: sistemas de pago, ticketing, información al viajero, SAE, MaaS, ABT, EMV, contactless, GTFS, etc., • Formación en Ingeniería (Informática, Telecomunicaciones, Industrial u otras)., • Experiencia liderando equipos multidisciplinares., • Certificaciones PMP, SCRUM, ITIL (muy valoradas)., • Conocimiento técnico en arquitecturas modernas (API REST, microservicios, NoSQL, Ruby on Rails – nice to have)., • Nivel alto de inglés (imprescindible)., • Disponibilidad para viajar. 🧭 ¿Cuál será tu rol en el equipo? • Liderar proyectos tecnológicos complejos en el ámbito del transporte y la movilidad., • Gestionar la relación con clientes públicos, incluyendo contratos de larga duración., • Definir alcance, planificación, estimaciones, plazos y calidad de los proyectos., • Coordinar y liderar equipos técnicos y funcionales., • Gestionar la productividad, capacidades y evolución del equipo., • Participar en la elaboración de propuestas y en el desarrollo de negocio., • Asegurar la correcta ejecución y entrega de los proyectos, alineando expectativas y resultados. 🎯 ¿Qué te ofrecemos? • 💼 Contrato indefinido desde el primer día y participación en proyectos de alto impacto y visibilidad., • 📈 Plan de carrera individualizado y mentorizado, pensado para perfiles con ambición y visión de largo plazo., • 🧠 Formación continua y certificaciones alineadas con el mercado y tu desarrollo profesional., • 💰 Retribución competitiva, con revisiones anuales en función de desempeño y evolución., • 🏥 Beneficios sociales (seguro médico, seguro de vida, dietas y retribución flexible)., • 👩 💻 Modelo híbrido, flexibilidad horaria, jornada intensiva los viernes y durante el verano., • 🤝 Buen ambiente de equipo, con referentes técnicos y de gestión de los que aprender… y a los que también aportar., • 🏆 Top Employer & Cultura inclusiva En NTT DATA llevamos 10 años consecutivos siendo Top Employer en España, gracias a nuestro compromiso real con el desarrollo del talento, la conciliación y la diversidad. Creemos que cada persona es única, y que esa singularidad es la que impulsa la innovación y el crecimiento colectivo. Aquí podrás explorar, potenciar y desarrollar tu liderazgo en un entorno que apuesta por las personas y el impacto positivo. ¿Te unes a liderar la movilidad del mañana? #WeAreAllUnique #YouMakeUsUnique #Mobility #ProjectManagement #GreenDeal #FutureAtHeart

In a nutshell Position: Clinical Scientist Location: Madrid, Hibrid Want to know more? mAbxience is a global biopharmaceutical company committed to innovation and excellence in the development and manufacturing of biotechnological medicines. We operate with a strong focus on quality, regulatory compliance, and scientific rigor to improve patient outcomes worldwide. What are we looking for? The Clinical Scientist is a member of the Medical Department responsible for the execution of day-to-day medical and scientific activities within assigned clinical studies. The role supports the design, execution, and documentation of clinical trials under the accountability and strategic oversight of the Global Clinical Lead (GCL). This role is assigned to clinical development programs of sufficient complexity. In simplified programs where no Clinical Scientist is assigned (e.g. PK studies in healthy volunteers), the Global Clinical Lead will directly perform these operational medical activities 1. Operational Medical Oversight (Responsible) • Conduct ongoing medical review of clinical trials and report findings, risks, and recommendations to the Global Clinical Lead. - Perform routine AE/SAE medical review and follow-up in alignment with the Safety Medical Monitoring Plan. - Conduct medical monitoring activities including protocol deviations, eligibility assessments, and medication reviews. - Perform coding review and medical review of tables and listings. - Participate in internal and CRO medical meetings and support medical discussions with investigators. - Escalate safety signals, protocol concerns, and medical risks to the GCL. 2. Study Documentation & Data Review Support (Responsible) • Draft and support the review of Medical Management Plans, Medical Data Review Plans, and SAP-related medical sections. - Support interim and final data analyses by preparing medical review summaries. - Support sponsor execution of statistical dry runs. - Coordinate operational medical activities related to DSMB/IDMC under the direction and accountability of the GCL. 3. Study Design & Development Support • Contribute to the drafting and review of clinical study protocols, amendments, and informed consent forms. - Provide scientific input to study design discussions under GCL guidance. 4. Cross-Functional Medical Support • Act as first point of contact for day-to-day medical queries from Clinical Operations, Pharmacovigilance, and Regulatory Affairs. - Support routine safety activities in collaboration with the Pharmacovigilance Department. - Contribute to responses to regulatory queries and deficiency letters. - Assist in the development of scientific publications and congress materials. 5. Departmental Contribution & Development (CLOP, PV, Medical Affairs and regulatory,scientific) • Support development and maintenance of medical SOPs. - Participate in Medical Department meetings and educational initiatives. - Engage in structured training and continuous professional development. What do you need? • Medical Doctor. - Fluent in Spanish and English. - Minimum 1 year of clinical or research experience. - Foundational knowledge of clinical development and regulatory requirements. - Strong analytical, organizational, and communication skills. - Willingness to travel. Our benefits! ⏰ Flexible start time from Monday to Friday (full-time). Permanent contract. Attractive salary package. Life and accident insurance. ️ Ticket restaurant Benefits and Savings Club. Development plans, internal mobility policy. ⭐ Many more! What will the Selection process be like? ️ ➡️ Stay tuned to your phone and email! The first thing we will likely do is contact you through one of the two channels. ➡️ Prepare well! We will continue with an in-person/virtual interview depending on availability and what we agree upon; there may be one or two interviews in the process, and depending on the type of process, there may also be some kind of test. ➡️ Wait for the result! We care that you feel guided throughout each selection process and know what to expect from us, so we will always try to inform you of the status of the process. Do you think this offer is not for you? Follow us on social media like LinkedIn/Instagram and stay tuned for any offers we may release; the opportunity to be a new Insuder is waiting! #mAbxience #ClinicalStudyCoordinator #BiotechCareers COMMITMENT TO EQUAL OPPORTUNITIES mAbxience is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees regardless of gender, ethnicity, religion, sexual orientation, disability, or any other characteristic.

Are you looking for the next challenge in your career? Would you like to be part of an exciting highly qualified team of professionals in an international environment? We are currently looking for a qualified S ystems Engineer – Aircraft Systems & V&V to join cutting‑edge electric aviation program s. Join an international division and work alongside some of the most talented engineers and technicians from all over the world. Your Benefits Competitive Salary. Long‑term secure contract. International project exposure with top technologies. Possibility of working remotely with a flexible schedule. Integration in a highly qualified team of professionals. Travel abroad with your project. Specialized training and continuous professional development. Social benefits and flexible compensation plan. Role Overview You will support the development, certification, and verification of aircraft systems for electric aviation platforms (eVTOL, electric propulsion, cabin systems). The role sits at the intersection of systems engineering, safety, certification, and V&V, with hands‑on involvement across requirements definition, modeling, testing, and compliance demonstration at Component, System, and Aircraft levels. Responsibilities Systems Engineering & Requirements Develop, manage, and validate aircraft‑, system‑, and component‑level requirements. Generate and maintain requirements aligned with customer, regulatory, and certification needs. Ensure bidirectional traceability between requirements, verification methods, and compliance evidence. Manage requirements in ALM environments (Polarion). Provide design feedback related to safety, requirements completeness, and verification readiness. Safety & Certification Apply SAE ARP4754A and ARP4761 processes throughout the system lifecycle. Support Functional Hazard Assessments (FHA), Fault Tree Analysis (FTA), and FMEA. Participate in certification planning and compliance demonstrations. Interface with certification engineers and DERs to support FAA approval activities. Support certification programs under Part 23 / 27 / 33, including electric propulsion systems. Verification & Validation Author, execute, and maintain verification plans, procedures, and test reports. Define and execute requirements‑based test strategies at Component, System, and Aircraft levels. Coordinate and execute lab, integration, and system‑level tests. Verify systems including: vibrations, airframe, fuselage, interiors, doors, transparencies, ECS, interior lighting, smoke detection, and more. Ensure verification activities align with certification schedules. Track and report verification status with full traceability. Modeling, Analysis & Test Support Perform system behavior modeling for validation. Support test automation and data analysis. Ensure verification deliverables meet certification expectations. Minimum Qualifications Bachelor’s degree in Mechanical, Electrical, Software Engineering, or related field. 10+ years of experience on Part 23 or 27 aircraft or rotorcraft programs. Strong knowledge of: SAE ARP4754A SAE ARP4761 FAA Order 8110.4C RTCA DO‑160G, DO‑331, DO‑178C Experience with ARP4754A‑based verification. Experience with requirements‑based testing and traceability audits. Proficiency with ALM tools (Polarion, JIRA, Confluence). Experience with modeling tools (Onshape, SolidWorks, CATIA, etc.). Comfortable working in certification‑focused environments. Preferred Qualifications Experience with Part 23 Amendment 64, ASTM F3338, Part 33 certification, or electric propulsion systems. Familiarity with: Polarion ALM CATIA ANSYS Mil‑HDBK‑217 / Mil‑HDBK‑21 Reliability tools (PTC Windchill, Isograph, Relyence) Test & automation experience with LabVIEW, Python, and automation frameworks. Background in aerospace verification & validation. Experience in certifying environments (Part 23, 25, 27, 29 or DO‑based programs under EASA/FAA). Tools & Work Environment Google G‑Suite (Docs, Sheets, Slides, Drive, Calendar). Slack & collaborative engineering workflows. ALM‑driven, traceability‑heavy certification environment.

Are you looking for the next challenge in your career? Would you like to be part of an exciting highly qualified team of professionals in an international environment? We are currently looking for a qualified S ystems Engineer – Aircraft Systems & V&V to join cutting‑edge electric aviation program s. Join an international division and work alongside some of the most talented engineers and technicians from all over the world. Your Benefits Competitive Salary. Long‑term secure contract. International project exposure with top technologies. Possibility of working remotely with a flexible schedule. Integration in a highly qualified team of professionals. Travel abroad with your project. Specialized training and continuous professional development. Social benefits and flexible compensation plan. Role Overview You will support the development, certification, and verification of aircraft systems for electric aviation platforms (eVTOL, electric propulsion, cabin systems). The role sits at the intersection of systems engineering, safety, certification, and V&V, with hands‑on involvement across requirements definition, modeling, testing, and compliance demonstration at Component, System, and Aircraft levels. Responsibilities Systems Engineering & Requirements Develop, manage, and validate aircraft‑, system‑, and component‑level requirements. Generate and maintain requirements aligned with customer, regulatory, and certification needs. Ensure bidirectional traceability between requirements, verification methods, and compliance evidence. Manage requirements in ALM environments (Polarion). Provide design feedback related to safety, requirements completeness, and verification readiness. Safety & Certification Apply SAE ARP4754A and ARP4761 processes throughout the system lifecycle. Support Functional Hazard Assessments (FHA), Fault Tree Analysis (FTA), and FMEA. Participate in certification planning and compliance demonstrations. Interface with certification engineers and DERs to support FAA approval activities. Support certification programs under Part 23 / 27 / 33, including electric propulsion systems. Verification & Validation Author, execute, and maintain verification plans, procedures, and test reports. Define and execute requirements‑based test strategies at Component, System, and Aircraft levels. Coordinate and execute lab, integration, and system‑level tests. Verify systems including: vibrations, airframe, fuselage, interiors, doors, transparencies, ECS, interior lighting, smoke detection, and more. Ensure verification activities align with certification schedules. Track and report verification status with full traceability. Modeling, Analysis & Test Support Perform system behavior modeling for validation. Support test automation and data analysis. Ensure verification deliverables meet certification expectations. Minimum Qualifications Bachelor’s degree in Mechanical, Electrical, Software Engineering, or related field. 10+ years of experience on Part 23 or 27 aircraft or rotorcraft programs. Strong knowledge of: SAE ARP4754A SAE ARP4761 FAA Order 8110.4C RTCA DO‑160G, DO‑331, DO‑178C Experience with ARP4754A‑based verification. Experience with requirements‑based testing and traceability audits. Proficiency with ALM tools (Polarion, JIRA, Confluence). Experience with modeling tools (Onshape, SolidWorks, CATIA, etc.). Comfortable working in certification‑focused environments. Preferred Qualifications Experience with Part 23 Amendment 64, ASTM F3338, Part 33 certification, or electric propulsion systems. Familiarity with: Polarion ALM CATIA ANSYS Mil‑HDBK‑217 / Mil‑HDBK‑21 Reliability tools (PTC Windchill, Isograph, Relyence) Test & automation experience with LabVIEW, Python, and automation frameworks. Background in aerospace verification & validation. Experience in certifying environments (Part 23, 25, 27, 29 or DO‑based programs under EASA/FAA). Tools & Work Environment Google G‑Suite (Docs, Sheets, Slides, Drive, Calendar). Slack & collaborative engineering workflows. ALM‑driven, traceability‑heavy certification environment.

🚦 Únete a NTT DATA y lidera la movilidad del futuro En NTT DATA somos más de 190.000 profesionales en más de 50 países, conectados por una visión común: utilizar la tecnología para transformar la sociedad de forma sostenible, eficiente y responsable. Trabajamos en múltiples sectores —energía, industria, telecomunicaciones, banca, sector público, sanidad siempre desde la colaboración, la innovación y una mirada a largo plazo. 🌱 Green Deal & Sustainability | Movilidad Sostenible: Desde el equipo de Movilidad Sostenible, lideramos proyectos clave para la transformación del transporte público y la movilidad urbana. Acompañamos a administraciones y operadores en la digitalización del transporte, la implantación de sistemas inteligentes, y la evolución hacia modelos de movilidad más sostenibles, conectados y centrados en las personas. Buscamos perfiles con visión, liderazgo y experiencia, capaces de convertir la complejidad en impacto real. 💡 Buscamos: • Jefes/as de Proyecto – Project Managers IT con experiencia en movilidad, transporte y tecnología, que quieran liderar proyectos estratégicos y de gran escala, guiando a clientes públicos en su proceso de transformación digital. 🧩 ¿Qué nos gustaría que aportaras? • Experiencia demostrable gestionando grandes proyectos tecnológicos y de software, preferiblemente con clientes del sector público., • Experiencia en proyectos de transporte público y movilidad., • Conocimiento del ecosistema de movilidad: sistemas de pago, ticketing, información al viajero, SAE, MaaS, ABT, EMV, contactless, GTFS, etc., • Formación en Ingeniería (Informática, Telecomunicaciones, Industrial u otras)., • Experiencia liderando equipos multidisciplinares., • Certificaciones PMP, SCRUM, ITIL (muy valoradas)., • Conocimiento técnico en arquitecturas modernas (API REST, microservicios, NoSQL, Ruby on Rails – nice to have)., • Nivel alto de inglés (imprescindible)., • Disponibilidad para viajar. 🧭 ¿Cuál será tu rol en el equipo? • Liderar proyectos tecnológicos complejos en el ámbito del transporte y la movilidad., • Gestionar la relación con clientes públicos, incluyendo contratos de larga duración., • Definir alcance, planificación, estimaciones, plazos y calidad de los proyectos., • Coordinar y liderar equipos técnicos y funcionales., • Gestionar la productividad, capacidades y evolución del equipo., • Participar en la elaboración de propuestas y en el desarrollo de negocio., • Asegurar la correcta ejecución y entrega de los proyectos, alineando expectativas y resultados. 🎯 ¿Qué te ofrecemos? • 💼 Contrato indefinido desde el primer día y participación en proyectos de alto impacto y visibilidad., • 📈 Plan de carrera individualizado y mentorizado, pensado para perfiles con ambición y visión de largo plazo., • 🧠 Formación continua y certificaciones alineadas con el mercado y tu desarrollo profesional., • 💰 Retribución competitiva, con revisiones anuales en función de desempeño y evolución., • 🏥 Beneficios sociales (seguro médico, seguro de vida, dietas y retribución flexible)., • 👩 💻 Modelo híbrido, flexibilidad horaria, jornada intensiva los viernes y durante el verano., • 🤝 Buen ambiente de equipo, con referentes técnicos y de gestión de los que aprender… y a los que también aportar., • 🏆 Top Employer & Cultura inclusiva En NTT DATA llevamos 10 años consecutivos siendo Top Employer en España, gracias a nuestro compromiso real con el desarrollo del talento, la conciliación y la diversidad. Creemos que cada persona es única, y que esa singularidad es la que impulsa la innovación y el crecimiento colectivo. Aquí podrás explorar, potenciar y desarrollar tu liderazgo en un entorno que apuesta por las personas y el impacto positivo. ¿Te unes a liderar la movilidad del mañana? #WeAreAllUnique #YouMakeUsUnique #Mobility #ProjectManagement #GreenDeal #FutureAtHeart

Amaris is looking for a Data Manager with strong experience in clinical data management for CRO environments. The position focuses on supervising data management activities to ensure the smooth progress and quality of clinical projects. 🔥 Your Responsibilities • Act as the main point of contact for all data management topics and participate in project/study meetings, • Contribute to the selection of subcontractors by preparing specifications and evaluating proposals, • Participate in study design, including data management sections in protocols and CRF specifications, • Oversee outsourced data management activities, ensuring compliance with cost, timelines, and data quality, • Validate deliverables such as data management plans, validation plans, transfer specifications, eCRF completion guides, and coding instructions, • Test eCRF before production deployment and after each protocol amendment, • Implement targeted quality control of data based on risk assessment, • Monitor progress of data management steps (entry, cleaning, coding, external data transfers, SAE reconciliation, etc.), • Approve SDTM specifications and verify SDTM packages as needed, • Regularly assess subcontractor service quality, establish action plans for deviations, and discuss corrective measures, • Participate in data review meetings and validate associated reports, • Ensure responsibility for database lock and unlock, verifying all prerequisites, • Provide statisticians with data for statistical analysis, • Verify the presence of all data management documentation in the Trial Master File (TMF) 🎯 Your Qualifications • Experience in clinical data management for CROs (5–10 years), • Proficiency with industry-standard data management tools and software, • Academic background in Life Sciences, Pharmacy, or related field, • English fluent. French is a plus., • You demonstrate strong analytical and problem-solving skills, • You demonstrate excellent communication skills 💡 What You’ll Get From Us • An international community bringing together 110+ different nationalities, • An environment where trust has a central place: 70% of our key leaders started their careers at the first level of responsibilities, • A robust training system with our internal Academy and 250+ available modules, • A vibrant workplace that frequently gathers for internal events (afterworks, team buildings, etc.), • At Mantu, sustainability is part of everything we do. You’ll have the opportunity to turn your ideas into action and make a tangible impact. Every day, our teams bring our ESG commitments to life, from reducing our footprint to driving positive change within our communities. Through our WeCare Together program, you’ll be empowered to design and lead projects that create real social or environmental impact, with the company’s full support. Amaris Consulting is proud to be an equal-opportunity workplace. We are committed to promoting diversity within the workforce and creating an inclusive working environment. For this purpose, we welcome applications from all qualified candidates regardless of gender, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics.

In a nutshell 📌 Position: Clinical Scientist Location: Madrid, Hibrid Want to know more? 👇 mAbxience is a global biopharmaceutical company committed to innovation and excellence in the development and manufacturing of biotechnological medicines. We operate with a strong focus on quality, regulatory compliance, and scientific rigor to improve patient outcomes worldwide. What are we looking for? 🔎 The Clinical Scientist is a member of the Medical Department responsible for the execution of day-to-day medical and scientific activities within assigned clinical studies. The role supports the design, execution, and documentation of clinical trials under the accountability and strategic oversight of the Global Clinical Lead (GCL). This role is assigned to clinical development programs of sufficient complexity. In simplified programs where no Clinical Scientist is assigned (e.g. PK studies in healthy volunteers), the Global Clinical Lead will directly perform these operational medical activities 1. Operational Medical Oversight (Responsible) • Conduct ongoing medical review of clinical trials and report findings, risks, and recommendations to the Global Clinical Lead., • Perform routine AE/SAE medical review and follow-up in alignment with the Safety Medical Monitoring Plan., • Conduct medical monitoring activities including protocol deviations, eligibility assessments, and medication reviews., • Perform coding review and medical review of tables and listings., • Participate in internal and CRO medical meetings and support medical discussions with investigators., • Escalate safety signals, protocol concerns, and medical risks to the GCL. 2. Study Documentation & Data Review Support (Responsible) • Draft and support the review of Medical Management Plans, Medical Data Review Plans, and SAP-related medical sections., • Support interim and final data analyses by preparing medical review summaries., • Support sponsor execution of statistical dry runs., • Coordinate operational medical activities related to DSMB/IDMC under the direction and accountability of the GCL. 3. Study Design & Development Support • Contribute to the drafting and review of clinical study protocols, amendments, and informed consent forms., • Provide scientific input to study design discussions under GCL guidance. 4. Cross-Functional Medical Support • Act as first point of contact for day-to-day medical queries from Clinical Operations, Pharmacovigilance, and Regulatory Affairs., • Support routine safety activities in collaboration with the Pharmacovigilance Department., • Contribute to responses to regulatory queries and deficiency letters., • Assist in the development of scientific publications and congress materials. 5. Departmental Contribution & Development (CLOP, PV, Medical Affairs and regulatory,scientific) • Support development and maintenance of medical SOPs., • Participate in Medical Department meetings and educational initiatives., • Engage in structured training and continuous professional development. What do you need? 🤓 • Medical Doctor., • Fluent in Spanish and English., • Minimum 1 year of clinical or research experience., • Foundational knowledge of clinical development and regulatory requirements., • Strong analytical, organizational, and communication skills., • Willingness to travel. Our benefits! 👏 • ⏰ Flexible start time from Monday to Friday (full-time)., • 📜 Permanent contract., • 💸 Attractive salary package., • 🥼 Life and accident insurance., • 🍽️ Ticket restaurant, • 💸 Benefits and Savings Club., • 📈 Development plans, internal mobility policy., • ⭐ Many more! What will the Selection process be like? 🕵️ ➡️ Stay tuned to your phone and email! The first thing we will likely do is contact you through one of the two channels. ➡️ Prepare well! We will continue with an in-person/virtual interview depending on availability and what we agree upon; there may be one or two interviews in the process, and depending on the type of process, there may also be some kind of test. ➡️ Wait for the result! We care that you feel guided throughout each selection process and know what to expect from us, so we will always try to inform you of the status of the process. 🔷 Do you think this offer is not for you? 🔷 Follow us on social media like LinkedIn/Instagram and stay tuned for any offers we may release; the opportunity to be a new Insuder is waiting! #mAbxience #ClinicalStudyCoordinator #BiotechCareers COMMITMENT TO EQUAL OPPORTUNITIES mAbxience is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees regardless of gender, ethnicity, religion, sexual orientation, disability, or any other characteristic.

In a nutshell 📌 Position: Clinical Scientist Location: Madrid, Hibrid Want to know more? 👇 mAbxience is a global biopharmaceutical company committed to innovation and excellence in the development and manufacturing of biotechnological medicines. We operate with a strong focus on quality, regulatory compliance, and scientific rigor to improve patient outcomes worldwide. What are we looking for? 🔎 The Clinical Scientist is a member of the Medical Department responsible for the execution of day-to-day medical and scientific activities within assigned clinical studies. The role supports the design, execution, and documentation of clinical trials under the accountability and strategic oversight of the Global Clinical Lead (GCL). This role is assigned to clinical development programs of sufficient complexity. In simplified programs where no Clinical Scientist is assigned (e.g. PK studies in healthy volunteers), the Global Clinical Lead will directly perform these operational medical activities 1. Operational Medical Oversight (Responsible) • Conduct ongoing medical review of clinical trials and report findings, risks, and recommendations to the Global Clinical Lead., • Perform routine AE/SAE medical review and follow-up in alignment with the Safety Medical Monitoring Plan., • Conduct medical monitoring activities including protocol deviations, eligibility assessments, and medication reviews., • Perform coding review and medical review of tables and listings., • Participate in internal and CRO medical meetings and support medical discussions with investigators., • Escalate safety signals, protocol concerns, and medical risks to the GCL. 2. Study Documentation & Data Review Support (Responsible) • Draft and support the review of Medical Management Plans, Medical Data Review Plans, and SAP-related medical sections., • Support interim and final data analyses by preparing medical review summaries., • Support sponsor execution of statistical dry runs., • Coordinate operational medical activities related to DSMB/IDMC under the direction and accountability of the GCL. 3. Study Design & Development Support • Contribute to the drafting and review of clinical study protocols, amendments, and informed consent forms., • Provide scientific input to study design discussions under GCL guidance. 4. Cross-Functional Medical Support • Act as first point of contact for day-to-day medical queries from Clinical Operations, Pharmacovigilance, and Regulatory Affairs., • Support routine safety activities in collaboration with the Pharmacovigilance Department., • Contribute to responses to regulatory queries and deficiency letters., • Assist in the development of scientific publications and congress materials. 5. Departmental Contribution & Development (CLOP, PV, Medical Affairs and regulatory,scientific) • Support development and maintenance of medical SOPs., • Participate in Medical Department meetings and educational initiatives., • Engage in structured training and continuous professional development. What do you need? 🤓 • Medical Doctor., • Fluent in Spanish and English., • Minimum 1 year of clinical or research experience., • Foundational knowledge of clinical development and regulatory requirements., • Strong analytical, organizational, and communication skills., • Willingness to travel. Our benefits! 👏 • ⏰ Flexible start time from Monday to Friday (full-time)., • 📜 Permanent contract., • 💸 Attractive salary package., • 🥼 Life and accident insurance., • 🍽️ Ticket restaurant, • 💸 Benefits and Savings Club., • 📈 Development plans, internal mobility policy., • ⭐ Many more! What will the Selection process be like? 🕵️ ➡️ Stay tuned to your phone and email! The first thing we will likely do is contact you through one of the two channels. ➡️ Prepare well! We will continue with an in-person/virtual interview depending on availability and what we agree upon; there may be one or two interviews in the process, and depending on the type of process, there may also be some kind of test. ➡️ Wait for the result! We care that you feel guided throughout each selection process and know what to expect from us, so we will always try to inform you of the status of the process. 🔷 Do you think this offer is not for you? 🔷 Follow us on social media like LinkedIn/Instagram and stay tuned for any offers we may release; the opportunity to be a new Insuder is waiting! #mAbxience #ClinicalStudyCoordinator #BiotechCareers COMMITMENT TO EQUAL OPPORTUNITIES mAbxience is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees regardless of gender, ethnicity, religion, sexual orientation, disability, or any other characteristic.

Amaris is looking for a Data Manager with strong experience in clinical data management for CRO environments. The position focuses on supervising data management activities to ensure the smooth progress and quality of clinical projects. 🔥 Your Responsibilities • Act as the main point of contact for all data management topics and participate in project/study meetings, • Contribute to the selection of subcontractors by preparing specifications and evaluating proposals, • Participate in study design, including data management sections in protocols and CRF specifications, • Oversee outsourced data management activities, ensuring compliance with cost, timelines, and data quality, • Validate deliverables such as data management plans, validation plans, transfer specifications, eCRF completion guides, and coding instructions, • Test eCRF before production deployment and after each protocol amendment, • Implement targeted quality control of data based on risk assessment, • Monitor progress of data management steps (entry, cleaning, coding, external data transfers, SAE reconciliation, etc.), • Approve SDTM specifications and verify SDTM packages as needed, • Regularly assess subcontractor service quality, establish action plans for deviations, and discuss corrective measures, • Participate in data review meetings and validate associated reports, • Ensure responsibility for database lock and unlock, verifying all prerequisites, • Provide statisticians with data for statistical analysis, • Verify the presence of all data management documentation in the Trial Master File (TMF) 🎯 Your Qualifications • Experience in clinical data management for CROs (5–10 years), • Proficiency with industry-standard data management tools and software, • Academic background in Life Sciences, Pharmacy, or related field, • English fluent. French is a plus., • You demonstrate strong analytical and problem-solving skills, • You demonstrate excellent communication skills 💡 What You’ll Get From Us • An international community bringing together 110+ different nationalities, • An environment where trust has a central place: 70% of our key leaders started their careers at the first level of responsibilities, • A robust training system with our internal Academy and 250+ available modules, • A vibrant workplace that frequently gathers for internal events (afterworks, team buildings, etc.), • At Mantu, sustainability is part of everything we do. You’ll have the opportunity to turn your ideas into action and make a tangible impact. Every day, our teams bring our ESG commitments to life, from reducing our footprint to driving positive change within our communities. Through our WeCare Together program, you’ll be empowered to design and lead projects that create real social or environmental impact, with the company’s full support. Amaris Consulting is proud to be an equal-opportunity workplace. We are committed to promoting diversity within the workforce and creating an inclusive working environment. For this purpose, we welcome applications from all qualified candidates regardless of gender, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics.

🚦 Únete a NTT DATA y lidera la movilidad del futuro En NTT DATA somos más de 190.000 profesionales en más de 50 países, conectados por una visión común: utilizar la tecnología para transformar la sociedad de forma sostenible, eficiente y responsable. Trabajamos en múltiples sectores —energía, industria, telecomunicaciones, banca, sector público, sanidad siempre desde la colaboración, la innovación y una mirada a largo plazo. 🌱 Green Deal & Sustainability | Movilidad Sostenible: Desde el equipo de Movilidad Sostenible, lideramos proyectos clave para la transformación del transporte público y la movilidad urbana. Acompañamos a administraciones y operadores en la digitalización del transporte, la implantación de sistemas inteligentes, y la evolución hacia modelos de movilidad más sostenibles, conectados y centrados en las personas. Buscamos perfiles con visión, liderazgo y experiencia, capaces de convertir la complejidad en impacto real. 💡 Buscamos: • Jefes/as de Proyecto – Project Managers IT con experiencia en movilidad, transporte y tecnología, que quieran liderar proyectos estratégicos y de gran escala, guiando a clientes públicos en su proceso de transformación digital. 🧩 ¿Qué nos gustaría que aportaras? • Experiencia demostrable gestionando grandes proyectos tecnológicos y de software, preferiblemente con clientes del sector público., • Experiencia en proyectos de transporte público y movilidad., • Conocimiento del ecosistema de movilidad: sistemas de pago, ticketing, información al viajero, SAE, MaaS, ABT, EMV, contactless, GTFS, etc., • Formación en Ingeniería (Informática, Telecomunicaciones, Industrial u otras)., • Experiencia liderando equipos multidisciplinares., • Certificaciones PMP, SCRUM, ITIL (muy valoradas)., • Conocimiento técnico en arquitecturas modernas (API REST, microservicios, NoSQL, Ruby on Rails – nice to have)., • Nivel alto de inglés (imprescindible)., • Disponibilidad para viajar. 🧭 ¿Cuál será tu rol en el equipo? • Liderar proyectos tecnológicos complejos en el ámbito del transporte y la movilidad., • Gestionar la relación con clientes públicos, incluyendo contratos de larga duración., • Definir alcance, planificación, estimaciones, plazos y calidad de los proyectos., • Coordinar y liderar equipos técnicos y funcionales., • Gestionar la productividad, capacidades y evolución del equipo., • Participar en la elaboración de propuestas y en el desarrollo de negocio., • Asegurar la correcta ejecución y entrega de los proyectos, alineando expectativas y resultados. 🎯 ¿Qué te ofrecemos? • 💼 Contrato indefinido desde el primer día y participación en proyectos de alto impacto y visibilidad., • 📈 Plan de carrera individualizado y mentorizado, pensado para perfiles con ambición y visión de largo plazo., • 🧠 Formación continua y certificaciones alineadas con el mercado y tu desarrollo profesional., • 💰 Retribución competitiva, con revisiones anuales en función de desempeño y evolución., • 🏥 Beneficios sociales (seguro médico, seguro de vida, dietas y retribución flexible)., • 👩 💻 Modelo híbrido, flexibilidad horaria, jornada intensiva los viernes y durante el verano., • 🤝 Buen ambiente de equipo, con referentes técnicos y de gestión de los que aprender… y a los que también aportar., • 🏆 Top Employer & Cultura inclusiva En NTT DATA llevamos 10 años consecutivos siendo Top Employer en España, gracias a nuestro compromiso real con el desarrollo del talento, la conciliación y la diversidad. Creemos que cada persona es única, y que esa singularidad es la que impulsa la innovación y el crecimiento colectivo. Aquí podrás explorar, potenciar y desarrollar tu liderazgo en un entorno que apuesta por las personas y el impacto positivo. ¿Te unes a liderar la movilidad del mañana? #WeAreAllUnique #YouMakeUsUnique #Mobility #ProjectManagement #GreenDeal #FutureAtHeart

Are you looking for the next challenge in your career? Would you like to be part of an exciting highly qualified team of professionals in an international environment? Sea uno de los primeros solicitantes, lea la descripción completa del puesto a continuación y luego envíe su candidatura para que sea considerada. We are currently looking for a qualified Systems Engineer – Aircraft Systems & V& V to join cutting‐edge electric aviation programs. Join an international division and work alongside some of the most talented engineers and technicians from all over the world. Your Benefits Competitive Salary. Long‐term secure contract. International project exposure with top technologies. Possibility of working remotely with a flexible schedule. Integration in a highly qualified team of professionals. Travel abroad with your project. Specialized training and continuous professional development. Social benefits and flexible compensation plan. Role Overview You will support the development, certification, and verification of aircraft systems for electric aviation platforms (e VTOL, electric propulsion, cabin systems). The role sits at the intersection of systems engineering, safety, certification, and V& V, with hands‐on involvement across requirements definition, modeling, testing, and compliance demonstration at Component, System, and Aircraft levels. Responsibilities Systems Engineering & Requirements Develop, manage, and validate aircraft‐, system‐, and component‐level requirements. Generate and maintain requirements aligned with customer, regulatory, and certification needs. Ensure bidirectional traceability between requirements, verification methods, and compliance evidence. Manage requirements in ALM environments (Polarion). Provide design feedback related to safety, requirements completeness, and verification readiness. Safety & Certification Apply SAE ARP4754 A and ARP4761 processes throughout the system lifecycle. Support Functional Hazard Assessments (FHA), Fault Tree Analysis (FTA), and FMEA. Participate in certification planning and compliance demonstrations. Interface with certification engineers and DERs to support FAA approval activities. Support certification programs under Part 23 / 27 / 33, including electric propulsion systems. Verification & Validation Author, execute, and maintain verification plans, procedures, and test reports. Define and execute requirements‐based test strategies at Component, System, and Aircraft levels. Coordinate and execute lab, integration, and system‐level tests. Verify systems including: vibrations, airframe, fuselage, interiors, doors, transparencies, ECS, interior lighting, smoke detection, and more. Ensure verification activities align with certification schedules. Track and report verification status with full traceability. Modeling, Analysis & Test Support Perform system behavior modeling for validation. Support test automation and data analysis. Ensure verification deliverables meet certification expectations. Minimum Qualifications Bachelor's degree in Mechanical, Electrical, Software Engineering, or related field. 10+ years of experience on Part 23 or 27 aircraft or rotorcraft programs. Strong knowledge of: SAE ARP4754 A SAE ARP4761 FAA Order 8110.4 C RTCA DO‐160 G, DO‐331, DO‐178 C Experience with ARP4754 A‐based verification. Experience with requirements‐based testing and traceability audits. Proficiency with ALM tools (Polarion, JIRA, Confluence). Experience with modeling tools (Onshape, Solid Works, CATIA, etc.). Comfortable working in certification‐focused environments. Preferred Qualifications Experience with Part 23 Amendment 64, ASTM F3338, Part 33 certification, or electric propulsion systems. Familiarity with: Polarion ALM CATIA ANSYS Mil‐HDBK‐217 / Mil‐HDBK‐21 Reliability tools (PTC Windchill, Isograph, Relyence) Test & automation experience with Lab VIEW, Python, and automation frameworks. Background in aerospace verification & validation. Experience in certifying environments (Part 23, 25, 27, 29 or DO‐based programs under EASA/FAA). Tools & Work Environment Google G‐Suite (Docs, Sheets, Slides, Drive, Calendar). Slack & collaborative engineering workflows. xcskxlj ALM‐driven, traceability‐heavy certification environment.

Are you looking for the next challenge in your career? Would you like to be part of an exciting highly qualified team of professionals in an international environment? We are currently looking for a qualified Systems Engineer – Aircraft Systems & V&V to join cutting‑edge electric aviation program s. Join an international division and work alongside some of the most talented engineers and technicians from all over the world. Your Benefits • Competitive Salary., • Long‑term secure contract., • International project exposure with top technologies., • Possibility of working remotely with a flexible schedule., • Integration in a highly qualified team of professionals., • Travel abroad with your project., • Specialized training and continuous professional development., • Social benefits and flexible compensation plan. Role Overview You will support the development, certification, and verification of aircraft systems for electric aviation platforms (eVTOL, electric propulsion, cabin systems). The role sits at the intersection of systems engineering, safety, certification, and V&V, with hands‑on involvement across requirements definition, modeling, testing, and compliance demonstration at Component, System, and Aircraft levels. Responsibilities Systems Engineering & Requirements • Develop, manage, and validate aircraft‑, system‑, and component‑level requirements., • Generate and maintain requirements aligned with customer, regulatory, and certification needs., • Ensure bidirectional traceability between requirements, verification methods, and compliance evidence., • Manage requirements in ALM environments (Polarion)., • Apply SAE ARP4754A and ARP4761 processes throughout the system lifecycle., • Support Functional Hazard Assessments (FHA), Fault Tree Analysis (FTA), and FMEA., • Participate in certification planning and compliance demonstrations., • Interface with certification engineers and DERs to support FAA approval activities., • Author, execute, and maintain verification plans, procedures, and test reports., • Define and execute requirements‑based test strategies at Component, System, and Aircraft levels., • Coordinate and execute lab, integration, and system‑level tests., • Verify systems including: vibrations, airframe, fuselage, interiors, doors, transparencies, ECS, interior lighting, smoke detection, and more., • Ensure verification activities align with certification schedules., • Perform system behavior modeling for validation., • Support test automation and data analysis., • Ensure verification deliverables meet certification expectations. Minimum Qualifications • Bachelor’s degree in Mechanical, Electrical, Software Engineering, or related field., • 10+ years of experience on Part 23 or 27 aircraft or rotorcraft programs., • Strong knowledge of:, • SAE ARP4754A, • SAE ARP4761, • FAA Order 8110.4C, • RTCA DO‑160G, DO‑331, DO‑178C, • Experience with ARP4754A‑based verification., • Experience with requirements‑based testing and traceability audits., • Proficiency with ALM tools (Polarion, JIRA, Confluence)., • Experience with modeling tools (Onshape, SolidWorks, CATIA, etc.)., • Comfortable working in certification‑focused environments. Preferred Qualifications • Experience with Part 23 Amendment 64, ASTM F3338, Part 33 certification, or electric propulsion systems., • Familiarity with:, • Polarion ALM, • CATIA, • ANSYS, • Mil‑HDBK‑217 / Mil‑HDBK‑21, • Reliability tools (PTC Windchill, Isograph, Relyence), • Test & automation experience with LabVIEW, Python, and automation frameworks., • Background in aerospace verification & validation., • Experience in certifying environments (Part 23, 25, 27, 29 or DO‑based programs under EASA/FAA). Tools & Work Environment • Google G‑Suite (Docs, Sheets, Slides, Drive, Calendar)., • Slack & collaborative engineering workflows., • ALM‑driven, traceability‑heavy certification environment.

Preparación y mantenimiento de Certificación SAE nivel 3, revisión 4 (fichas de especificación, acuerdos, solicitud de lista en terceros países, gestión de auto precintados, solicitud de exportación CEXGAN, y demás carga documental). Apoyo al responsable para mantener el sistema de gestión

Ayuda al camarero en la preparación y servicio de comidas y bebidas, asegurando la rapidez en las entregas y manteniendo el orden y la limpieza en el área de trabajo.