Formador/a Escuela de Ocio y Tiempo Libre - Cardahmomo

-EASA B1 or/and B2 CL215T Licensed Engineer or more than 7 years of experience on this type -Proven of experience as the previous role -Good level of English, Spanish is a plus

In few words Position: Senior Data Analyst & Clinical Data Manager Location: Madrid (onsite) Experience:+5 years of experience in similar positions in Pharma sector with experience at international level. 👇Global Responsibility The Senior Data Analyst & Clinical Data Manager is a hybrid role responsible for driving the development of reporting and visualization activities that enable data-driven decision-making across Exeltis’ portfolio of clinical studies, while leading and ensuring accountability in all data management activities related to clinical trial projects. This role is responsible for managing and overseeing all aspects of clinical trial data management, from study start-up to final database lock, while also delivering new solutions that optimize data workflows, facilitating the interpretation of clinical data trends, and ensuring compliance with regulatory and industry quality standards. Specific Responsibilities 📌 Data Analytics: • Analyzing and interpreting data to identify patterns that help drive decision-making in clinical trials., • Implementing clinical data standardization and developing new solutions to ensure optimal management and interpretation of the clinical data., • Developing key performance indicators (KPIs) to evaluate clinical trial progress., • Generating data visualization strategies and dashboards through the use of data from various databases and sources., • Collaborate cross-departmentally to develop new machine learning and artificial intelligence tools related to clinical data., • Ensuring that study team members from different functional areas understand and deliver components affecting data to ensure the successful execution of deliverables. Clinical Data Management For the clinical trials conducted internally (in-house model): • Serves as a primary point of contact for data management deliverables. Understands, mediates and solves issues related to data management study deliverables and escalates as required to Study Team or Manager (as applicable)., • Establishes strong communication with Study Team, functional leads and other stakeholders., • Provides data management operational input into the study design, protocol development, study planning, study documents including the study risk register., • Leads all data management aspects of a clinical study, including study planning, start-up activities, conduct and database lock., • Ensures data management study deliverables are in compliance with applicable SOPs and regulatory guidelines., • Creates or reviews study level timelines for data management deliverables and ensures they are met on time., • Develops study-specific electronic data capture (EDC) systems: electronic case report form (eCRF) specifications, edit checks specifications., • Validates and tests clinical database during User Acceptance Testing., • Creates key functional plans and specifications, tailored to the study needs (e.g. Data Management Plan, eCRF Completion Guidelines, Data Review Plan)., • Develops data transfer agreements and specifications with vendors providing external data (e.g. laboratory results)., • Develops or provides support to Study Team in the development of other external systems capturing clinical data, e.g. ePRO/eCOA, RTSM/IRT and ensures that any data transfer requirements between the systems are documented and tested appropriately., • Conducts training for site users/monitors/other study team members on some of the clinical systems, e.g. EDC, RTSM, eCOA., • Manages user accounts in clinical systems governed by data management (activates / de-activates users in the database in response to requests e.g. from Project Manager or Trial Manager)., • Performs review / data cleaning activities such as, but not limited to, study team data reviews, edit check and manual queries review, coding, SAE reconciliation and non-eCRF data reconciliation (e.g. lab data, eCOA/ePRO)., • Supports coding of medical terms in the clinical database, if required., • Evaluates different options and uses careful judgment to choose the most efficient and effective way to resolve issues that arise during study lifetime., • Generates data listings and reports needed for data review by the other Study Team members., • Monitors study status (e.g. enrollment, eCRFs completion, query rates) on an ongoing basis and provides data status reports to the Study Team., • Updates applicable databases, as a result of change order and protocol amendment(s)., • Prepares/reviews database for data freeze and/or lock and archives it with related documentation., • Providing feedback on SDTM datasets to ensure data are collected and represented in a manner that supports regulatory requirements to comply with CDISC standards (CDASH, SDTM and ADaM)., • Review the final SDTM, define.xml, annotated CRF and Clinical Study Data Reviewer’s Guides for EMA, FDA and PMDA submissions., • Ensures that data management documentation is complete and up-to date in the electronic trial master file (eTMF). For clinical trials where any of the above activities have been outsourced to an external service provider: • Oversees / manages the vendor to ensure that timelines and deliverables meet Exeltis and protocol requirements., • Ensures that their work is done in accordance with effective work orders and Exeltis SOPs (if applicable)., • Participates in and supports RFP process (review RFP documents, pricing, evaluates the needs)., • Performs quality controls according to applicable plans, e.g. Data Management Plan, Data Review Plan., • Review the creation and final SDTM, define.xml, annotated CRF and Clinical Study Data Reviewer’s Guides for EMA, FDA and PMDA submissions. Other: • Develops SOPs or guidelines to ensure data management activities are in accordance with Good Clinical Practice (GCP) and any other applicable regulations or local requirements., • Promotes the implementation of clinical data standards to increase consistency, efficiency & productivity (creation of eCRF standards, documents/plans templates etc)., • Provides input into activities associated with regulatory inspections / audits for assigned studies., • Provides input into activities associated with selection, validation and use of software systems, devices and vendors., • Mentors and trains junior data managers and data analyst; serves as Subject Matter Expert (SME). 🕵️Requirements and personal skills • Education: Bachelor’s Degree (or its international equivalent) in Life Science or Health Informatics., • Languages: Fluent English, knowledge of other languages will be an asset., • Experience (years/area): +5 years of experience in similar positions in Pharma sector with experience at international level., • Specific Knowledge: Strong understanding of Good Clinical Practice (GCP) guidelines and other relevant regulations (e.g., FDA, ICH, EMA). Strong working knowledge of data management tools and software. Knowledge of programming languages (e.g. Python, SQL), relational database terminology, reporting tools and data visualization software., • Travels: Willingness to travel 20%, • Personal skills: Demonstrated experience in managing multiple priorities in a highly dynamic environment.

¿Te apasiona liderar proyectos que cambian el futuro de la alimentación sostenible, la bioeconomía y la salud global? 🌍 En Yeeply, buscamos un/a Principal Investigator (PI) para liderar la estrategia científica y técnica de proyectos de investigación europeos e internacionales en el ámbito FoodTech, One Health y Bioeconomía. Tu misión será impulsar líneas de I+D de alto impacto, construir consorcios de excelencia y transformar la ciencia en innovación real para un sistema alimentario más sostenible, saludable y resiliente. 🍽️ 🚀 ¿Qué harás en tu día a día? 🔬 Liderazgo científico y técnico: • Diseñar, planificar y dirigir proyectos de investigación dentro del área de sistemas alimentarios sostenibles y bioinnovación., • Supervisar equipos de investigadores y técnicos, fomentando la colaboración y la excelencia científica., • Generar resultados tangibles: publicaciones, patentes y desarrollos tecnológicos transferibles a la industria o la sociedad., • Liderar la preparación de propuestas competitivas en programas como Horizon Europe, EIC, CBE-JU, LIFE o EDF, redactando secciones clave de Excelencia, Metodología e Impacto., • Coordinar la creación de consorcios internacionales con socios industriales, académicos e institucionales., • Dirigir la ejecución técnica de proyectos adjudicados, garantizando la entrega de hitos, resultados y KPIs., • Colaborar con los Project Managers en la planificación presupuestaria, gobernanza y reporting., • Promover la innovación responsable, el impacto y la sostenibilidad de los resultados. 🧠 ¿Qué puedes aportarnos? • Experiencia demostrada en redacción y coordinación de propuestas europeas de I+D (Horizon Europe o programas similares)., • Excelente capacidad de redacción científica en inglés (nivel C1 o superior)., • Experiencia estructurando y liderando consorcios internacionales y multidisciplinares., • Sólido conocimiento de los marcos europeos de investigación, su lógica de financiación y las vías de impacto., • Habilidades de gestión de proyectos, liderazgo y resolución de problemas., • Orientación a resultados, integridad y visión estratégica. 💡 Expertise específica – Food Systems & Bioeconomy: • Microbioma & One Health: ecología microbiana, interacciones huésped-entorno y modelos experimentales multiecosistema., • Multi-omics & Bioinformática: integración de datos de metagenómica, transcriptómica y metabolómica (R, Python, QIIME2, Nextflow…)., • Modelos in-vitro y Organ-on-Chip aplicados a nutrición, salud o toxicología., • Conocimientos en agronomía o fisiología humana/animal., • Gestión de datos FAIR, metadatos y plataformas digitales europeas (ELIXIR, MIRRI, EOSC). 🌟 Valoraremos especialmente si también cuentas con… • Trayectoria demostrable en proyectos del Cluster 6 de Horizon Europe (Food, Bioeconomy, Agriculture, Environment)., • Experiencia en partenariados público-privados o iniciativas como EIT Food, CBE-JU, LIFE o PRIMA., • Participación activa en plataformas europeas como Food for Life, BIOVEGEN o SusChem., • Publicaciones científicas, patentes o resultados tecnológicos en ciencia alimentaria, microbiología o bioeconomía., • Conocimientos en transferencia tecnológica, gestión de IPR y explotación de resultados. 🌱 ¿Por qué unirte a este proyecto? En Yeeply, la innovación tiene impacto real. Trabajamos codo con codo con centros de investigación aplicada que impulsa soluciones tecnológicas sostenibles para afrontar los grandes retos globales. Te integrarás en un entorno colaborativo, internacional y orientado a la excelencia, donde la ciencia se transforma en valor para la sociedad y la industria. 👉 Si buscas liderar la frontera entre la ciencia, la innovación y el impacto, este es tu lugar. Únete a un equipo que combina visión, talento y propósito. 🌟 ¿Qué te ofrecemos? 📜 Contrato indefinido + plan de retribución flexible 🏡 Modalidad Presencial en primer punto con evolución: Madrid Norte, Zona Cantoblanco 💙 Beneficios sociales: • Seguro médico y de vida 🏥, • Plus de teletrabajo 💻, • Formación continua con bonificaciones 🎓, • Ambiente colaborativo y oportunidades reales de crecimiento 🚀 Envíanos tu candidatura y crece con nosotros hacia el futuro de la alimentación sostenible y la bioeconomía europea. 🌍✨

Taketalent está colaborando con PharmaMar, Laboratorio Farmacéutico, líder a nivel mundial en investigación y desarrollo de medicamentos innovadores de origen marino para el área terapéutica de oncología. Actualmente estamos en búsqueda de un/a Técnico/a de Control de Calidad para un puesto de carácter totalmente presencial. La misión del puesto consiste en asegurar la ejecución del plan de trabajo diario de ensayos microbiológicos y físico-químicos dando soporte microbiológico al área de Microbiología. Funciones: • Supervisar de forma continua el cumplimiento de los estándares y prácticas de trabajo propios del laboratorio en materia de calidad y seguridad en el trabajo., • Colaborar con el Jefe de Control de Calidad en el diseño e implantación del Sistema de Calidad que asegure el cumplimiento de los requisitos GMP aplicables., • Asegurar la ejecución del programa de trabajo diario., • Soporte técnico a análisis microbiológicos., • Supervisión de la monitorización ambiental y de instalaciones (planta de agua, gases técnicos) de la planta., • Revisión de los resultados de ensayo, sistemas informatizados y cuadernos de laboratorio., • Informar al Jefe de Control de Calidad de cualquier condición adversa a la calidad detectada en la ejecución de los ensayos., • Participar en las investigación de los resultados OOS, investigaciones microbiológicas, desviaciones, controles de cambios y gestionar la puesta en marcha de acciones correctoras / preventivas., • Colaborar en la formación en el puesto de trabajo y cualificación de analistas., • Asegurar que los equipos se mantienen, calibran, cualifican o re-cualifican en las fechas previstas., • Asegurar que se cumplen las medidas de seguridad establecidas., • Proponer acciones de mejora de la Calidad y Seguridad. Requisitos: • Licenciatura Ciencias de la Salud, Farmacia o Química o experiencia previa en análisis microbiológicos que avale el desempeño de las funciones anteriormente descritas. Deseable formación adicional en análisis físico-químicos., • Nivel de inglés alto, • Formación específica y al menos dos años en un puesto de técnico en un laboratorio de ensayos microbiológicos. Qué se ofrece • Salario bruto anual competitivo + variable vinculado a objetivos., • Paquete de beneficios sociales (seguro médico privado, plan de acciones, comedor de empresa, formación continua, entre otros)., • Horario de entrada flexible y viernes de jornada intensiva., • Un entorno de trabajo dinámico, colaborativo y enfocado en la innovación, con oportunidades de desarrollo profesional., • Un compromiso firme con la diversidad, la igualdad de oportunidades y un entorno inclusivo. ¿Te interesa dar el siguiente paso en tu carrera dentro de una compañía referente en innovación y oncología? Queremos conocerte.

We are seeking a Clinical Project Manager In the UK for international observational field studies and secondary data studies to join our team in Madrid. Applications from senior project associates acting as project managers shall also be considered. • Interviews with shortlisted candidates will be held in February 2026. OXON Epidemiology is a niche, late-phase international Contract Research Organisation (CRO) with Operations centred in our Madrid office, and home-based staff in the UK and USA. If you are looking to make an impact in a growing company and help to shape its growth, this is the place to be. By working in OXON, you can further your career in a dynamic, fast-paced, learning environment, be innovative and make an impact. Key elements of what OXON provides: • Close involvement with world-class science (epidemiologists and statisticians, hybrid field-database studies, and an eminent Professor of Medical Statistics, who visits Madrid monthly.), • Involvement in all aspects of field studies and secondary data studies, as well as pure operational areas: proposal, bid defence, protocol, SAP, eCRF development, PV, analyses, reports, manuscripts., • Deeper involvement in fewer studies rather than lots of studies., • Ability to implement your ideas and make improvements., • Maintain relationships by meeting F2F with your team(s) (frequency of visits to the Madrid office determined by whether you live in or away from Madrid) in a friendly, learning, fun environment., • A horizontal company, with access to upper management., • A passion for science and improving patient care, with medics who still see patients. You will receive broad experience in multi-country observational studies. You will have the opportunity to stay close to the science and interact closely with epidemiologists, medics, statisticians, data managers, EDC software developers, PV, as well the Operations group, and be involved in innovative developments in observational research, such as hybrid field-database studies and pragmatic trials, with leading academics in London, Oxford, and other EU countries. This experience is provided in a supportive, learning environment that will allow you to develop more rapidly than in a narrow silo-based job. We genuinely care about our people, and they share in our success. JOB DESCRIPTION: The successful candidate will have the chance to work across several non-interventional field and secondary data studies within numerous therapeutic indications. As a Clinical Project Manager, you will be responsible for the overall execution of the project, managing cross-functional teams across the organisation and acting as the principal liaison with the client to ensure the project is completed on time, within budget and with the expected level of quality. Responsibilities: • Managing and leading a Project Team., • Ensuring that the Project Team completes the project on budget, on schedule and within the scope., • Monitoring of project progress and level of performance., • Checking project progress toward its objectives, determining the cause of any deviations from the plan, and taking corrective actions to address these deviations., • Developing and maintaining a detailed Project Plan with the team and managing the team’s performance of project tasks., • Managing project deliverables in line with the Project Plan., • Managing project resources and availability according to the different project phases., • Key contact for client management., • Efficient communication throughout the entire project life, including the preparation of status reports on a regular basis, organisation of internal and external meetings and escalation of issues that cannot be resolved by the Project Team., • Keeping track of project issues and escalation where appropriate., • Coordinating activities across different organizational departments, • Participation in proposals and bid defences. Requirements: • Bachelor’s degree in health sciences, life sciences or related discipline is required; master’s degree is preferred or equivalent combination of education, training and experience., • Fluency in English (spoken and written)., • A minimum of 2–3 years of experience as Project Associate / Project Management Assistant or PM in a CRO or biopharmaceutical company., • Knowledge and experience working in international multi-country non-interventional studies/ pharmacoepidemiologic studies is preferred., • Knowledge of ICH, GPP and GCP guidelines, as well as European regulations., • Advanced computer skills including Office 365 (Word, PowerPoint, Excel) and other PM software., • Excellent communication skills (oral and written) and interpersonal skills., • Strong operational management with attention to detail., • Ability to lead a cross-functional team in a matrix environment., • Proven complex problem-solving and decision-making skills., • Ability and willingness to travel up to 10% of the time. WE OFFER: • Full-time, permanent contract., • Home-based position (with determined visits to the Madrid office.), • Flexible timetable., • A competitive salary according to experience., • Bonus scheme., • Health insurance., • Opportunities for career development and training., • Opportunities to participate in academic research., • An international working environment, working on international studies. OXON EPIDEMIOLOGY is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We encourage applications from candidates of all backgrounds and do not discriminate based on race, gender, age, religion, disability, sexual orientation, or any other protected status. Join us in building a diverse and talented team! COMPANY DESCRIPTION: OXON is a full service global scientific/operational service provider specialising in multi-country field, database, and hybrid observational studies, pragmatic trials and meta-analysis for safety, market access/HEOR and drug development. We have strong links with the prestigious London School of Hygiene & Tropical Medicine, and Oxford University, and are a preferred provider for several top-20 pharma companies. With offices in London and Madrid, OXON applies world-class epidemiological and operational experience and innovative technologies to help clients worldwide obtain high-quality (Lancet-hitting) real-world data with a passion for improving patient’s and public health. For more information, visit This job posting is published exclusively on LinkedIn and may not be reproduced, indexed, or redistributed on third-party job boards without prior written authorization.