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Tengo varias estanterías de madera y metal que requieren anclajes adecuados y tornillos compatibles con la pared de yeso laminado. Quisiera alguien responsable, con experiencia en bricolaje y que pueda evaluar el tipo de fijación según el peso que soportarán las estanterías. Busco a alguien par

Equity Research VP (Multisector)Country: SpainIT STARTS HERESantander () is evolving from a global, high-impact brand into a technology-driven organization, and our people are at the heart of this journey.Descubra exactamente qué habilidades, experiencia y cualificaciones necesitará para tener éx

Job Description:We are looking for a key player to transform our technological roadmaps into reality by identifying strategic public funding opportunities, building collaborative consortia, and securing public financing for our R&T projects in Spain.The position is functionally attached to the Head

Economic Research & Business Intelligence Sr. Preferred)Familiarity with generative artificial intelligence and automation tools applied to economic analysis and information processing. Our mission is to contribute to help more people and businesses prosper.

Use your creativity and design workshops to help employees gain confidence and fluency in English – For example involving TV shows films, current affairs, • Estudiantes Universitarios, de preferencia, alumn@s nativos de habla inglesa • Incorporación a través de la firma de Convenio de Práct

IQVIA’s Global Site Activation Team of 2000 employees, drives best in class site and customer experience, with industry leading outcomes. We keep the patient at the forefront; ‘Always Impatient for the Patient’ and we excel in our collaboration with our external/internal customers. IQVIA’s Country Site Activation team are a global network who identify and activate sites to the highest quality to ensure patients on Clinical trials have access to safe and effective medication. We are leaders in innovation and first to new technologies, meaning a vast amount of career development opportunities are available. As a Senior Site Activation Specialist, you will work and lead complex projects under general supervision, serve as Single Point of Contact in assigned studies for investigative sites, Site Activation Manager, Project Management team, and other departments as necessary. You will also ensure adherence to standard operating procedures (SOPs), Work Instructions, quality of designated deliverables and project timelines. You will perform feasibility, site ID, start up and site activation activities according to applicable regulations, SOPs and work instructions, along with distributing completed documents to sites and internal project team members. You will also prepare site documents and review for completeness and accuracy, along with reviewing, tracking, and following up the progress, the approval and execution of documents, questionnaires, CDA/SIF, regulatory, ethics, Informed Consent Form, and Investigator Pack release documents, in line with project timelines. Coupled with informing team members of completion of feasibility, site ID, regulatory and contractual documents for individual sites, and providing local expertise to SAMs and project team during initial and on-going project timeline planning. Along with performing quality control of documents provided by sites. You may also act as an SME on specific subjects, mentor junior CSAs, and have a sponsor-facing role. • Bachelor’s Degree in Life Sciences or related field, • Minimum 3 - 4 years’ prior experience in Clinical Research, including 1 year in a leadership capacity., • Experience with activities such as submissions to Ethics Committees and Regulatory Authorities, contract and budget negotiations, study start-up activities, and overall site activation processes., • Familiarity with the day-to-day responsibilities within Global Site Activation, • Strong problem solving skills, • Ability to negotiate and have strong communication skills, • Ability to work on multiple projects, • Knowledge of applicable functional/regulatory requirements, including local regulations, SOPs and ICH/GCP, • Exposure across 21 Therapeutic Areas, • Be part of a global team who operate across 141 locations, • Exposure across a variety of studies and projects, • Access to new, innovative technologies, • Work within a collaborative and vibrant environment, • Own your career! It takes passion to make the extraordinary possible for patients. Our culture of innovation and collaboration enables us to explore new possibilities and help improve health around the world. When you join our diverse, global team, you’ll harness the power of unparalleled data, advanced analytics, cutting-edge technologies, and deep healthcare and scientific expertise to drive healthcare forward. IQVIA 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 https://jobs.iqvia.com. IQVIA 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. At 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. #J-18808-Ljbffr

We're looking for an experienced program or operations manager who is native or fluent in Spanish to run delivery for a team of senior domain experts training and evaluating AI agents. You'll own throughput, quality and expert performance for the Spanish (Spain) cohort across finance, consulting, law, medicine, STEM and HR. Requirements • 5+ years running delivery programs, ideally expert-data, AI training or professional-services operations, • Native or fluent in Spanish, • Degree from a top-20 university in Spain, • Experience managing distributed teams of senior professionals, quality control and review workflows, and daily delivery targets Details: Remote, 40 hours per week, hourly, pilot running Oct 23 to Nov 19. #J-18808-Ljbffr

Relix water se encuentra en búsqueda de Maestro Segunda Mecánico con 2 años de experiencia en el cargo y faena minera.

IQVIA is seeking a Clinical Monitoring Analyst (Cluepoints) for a remote role. The CMA will work with the client to manage delivery, perform setup, programming and refreshes of the CM platform, and contribute to CMP execution. Strong SAS skills and communication are required. Role involves collaborating with a sponsor-driven project, maintaining CM specifications, and ensuring compliance with regulatory standards across study activities. #J-18808-Ljbffr

Messy spend management is tricky business. And tedious processes are a lose-lose situation for all involved, not just finance. At Pleo, we're changing that. We build spend solutions that make managing money seamless, empowering, and surprisingly effective for finance teams and employees alike - with a vision to help all businesses ‘go beyond’. The word ‘Pleo’ actually means ‘more than you’d expect’, and living by that mantra has been the secret to our success over the last 10 years. Now, we’re at a pivotal moment in our journey; every move we make has a direct impact on our 40,000+ customers, our business, and our collective success. We need people who take pride in uncovering customer needs, who turn complex problems into simple solutions, challenge the way things are done (respectfully), and always aim high. With great ambitions driving us forward, we can’t say we’ve got this whole thing figured out. And frankly, that’s half the fun! What we can say is that we’re a driven, progressive, and, importantly, a kind bunch of 850+ people from over 100 nationalities, all committed to delivering the future of business spending, together. We’re looking for a Senior Transaction Monitoring and Fraud Framework Specialist at Pleo in the first line of defence (1LoD). You’ll be the architect of our defence strategy across transaction surveillance and fraud, with a clear focus on leading innovation and embedding AI into how we detect, investigate, and prevent financial crime. This isn’t a purely reactive role. Within our Financial Crime Framework & Innovation team, you’ll run cross-functional projects that bring together Financial Crime Operations, Engineering, 2LoD, and leadership to design controls and processes that scale. You’ll translate emerging threats and regulatory expectations into practical, automated, and measurable interventions and controls — including the thoughtful use of AI tools to improve decision quality, reduce manual effort, and strengthen governance. • Lead innovation in transaction monitoring and fraud by identifying high-impact opportunities for automation, model/rule optimisation, and AI-assisted investigation workflows., • Run end-to-end change and delivery projects (discovery design build rollout monitoring), coordinating stakeholders across 1LoD/2LoD, Operations, Product, Engineering, and Data., • Design and maintain our financial crime frameworks, controls, and procedures, ensuring they remain effective as our products, customer base, and threat landscape evolve., • Partner with Engineering on the development, deployment, and lifecycle management of transaction surveillance and fraud rules and models, including performance monitoring, drift detection, and continuous tuning., • Integrate AI tools into processes responsibly, including:, • improving alert triage and case prioritisation,, • enhancing investigation quality and consistency,, • accelerating root cause analysis and emerging-risk discovery,, • strengthening documentation, auditability, and control testing., • Turn insights from transaction alerts and fraud cases into actionable improvements across the framework, leading with data to reduce false positives, close control gaps, improve prevention and improve coverage of complex typologies., • File SARs for all EEA customers., • Act as Pleo’s go-to transaction monitoring and fraud subject matter expert, sharing learnings on threats, regulatory developments (including AML/CTF), and industry best practice., • You’re a builder and a problem-solver who can turn strategy into operational reality. You’re comfortable in ambiguity, confident leading cross-functional delivery and taking on responsibility, and you have a track record of driving meaningful change transaction monitoring., • You’re a builder and a problem-solver who can turn strategy into operational reality. You’re comfortable in ambiguity, confident leading cross-functional delivery and taking on responsibility, and you have a track record of driving meaningful change transaction monitoring., • You have significant experience designing and improving transaction monitoring and fraud frameworks, controls, and operating models in a scaling or high-volume environment., • You have demonstrable experience leading innovation (for example: new monitoring approaches, automation, analytics improvements, or AI-enabled workflows) with measurable outcomes., • You are experienced in running projects and change initiatives, including stakeholder management, prioritisation, and delivery planning., • You’re hands‑on with data: you can interpret performance metrics, investigate root causes, and translate findings into clear requirements and control enhancements., • You understand the practical governance needs of AI‑enabled and automated controls (documentation, explainability, testing, risk acceptance, and audit … #J-18808-Ljbffr

WalksDevour is a high-end tour operator, delivering best-in-class food tours, special access sightseeing tours, and day trips across Europe and North America. Our team is remote and geographically-dispersed, but connected by a passion for creating core memories for our guests. Travel is an exciting industry but one of constant disruption. On any given day we're dealing with tour guides calling in sick last minute, site closures at major attractions, or rough waters on the Amalfi Coast. Our Guide & Guest Support Team are at the forefront of resolving these problems. They find replacement guides, work with guests to find alternative tours and times, or with operations to find and communicate alternative itineraries – all so our guests’ experiences are smooth on the surface (no matter how hard we paddle underwater). They also interface directly with guests on standard issues such as, helping them find their meeting points or reunite with their guides when lost. We're looking for an experienced leader to take ownership of this function. You'll work in a complex system of stakeholders including local operations, sales, marketing and technology. This is a service and operations role, not a sales role: your focus is resolving customer issues quickly, consistently and well. You will own the Guide & Guest Support Team end to end — people, processes, workforce planning and the Zendesk, Tour Optima and Talkdesk platforms that underpin them. You will turn data into decisions, keep service levels on target, and build a team that customers and colleagues can rely on. • Run daily contact centre operations across voice, email, chat and messaging channels., • Own and report on core KPIs: service level, average speed of answer, abandonment rate, AHT, first contact resolution, CSAT and NPS., • Monitor real-time queues and make intraday decisions to protect service levels., • Identify root causes of contact demand and work with other teams to reduce avoidable contacts., • Work with operations to ensure coverage for guide emergencies via Whatsapp and other communication channels, • Ensure we are fully up to date with all processes, workflows and documentation to ensure optimal resolution of all issues. Work with senior business leaders to elevate trends negatively impacting guests, • Empower Team Leads and Tier 2 agents to own the function of last-minute issue resolution., • Track instances of refunds and cancellations and work cross-functionally to improve customer and financial outcomes., • Forecast contact volumes and build schedules, rotas and staffing plans to match demand., • Manage shrinkage, adherence and occupancy, and plan for seasonal peaks., • Prepare headcount and budget proposals backed by data., • Act as the operational owner of Zendesk: ticket workflows, triggers, automations, macros, views, SLAs and reporting., • Act as the operational owner of Talkdesk: IVR and call flows, routing and queues, skills, real-time dashboards and call recording., • Keep both platforms configured to support efficient routing and accurate reporting, working with IT and vendors on changes and integrations., • Build dashboards and reports in Zendesk Explore and Talkdesk Live/Explore for leadership and the floor., • Mentor team leads to increase people management capacity and establish lines of succession & progression. Manage performance review process for all Guide & Guest Support staff and ensure development plans exist for all staff members., • Recruit and onboard new team members, and own the training programme., • Build an engaged, accountable culture in a remote-first team, and lead the transition to hybrid working., • Build relationships with leaders across the business and use them to unlock performance rather than to manage escalations, • Understand all the contributing factors of performance and make deliberate trade-offs between quality, capacity and cost, • Run the quality assurance programme: scorecards, call and ticket reviews, calibration and feedback., • Write and maintain SOPs, knowledge base content and escalation paths., • Lead continuous improvement projects using customer feedback and operational data., • Meet regularly with key stakeholders to gather feedback on team performance. Identify and action areas with opportunity for improvement., • Ensure compliance with GDPR, call-recording rules and internal policies., • 5+ years in contact centre or customer service operations, with at least 3 years managing teams through Team Leaders., • Experience leading through operational incidents or crises, knowing who to pull in across the business and how to drive resolution, • Experience with Zendesk, including configuring workflows, triggers, automations, SLAs and Explore reporting., • Experience with Talkdesk, including IVR and routing design, queue management and real-time and historical reporting., • Proven track record of hitting service-level, quality and efficiency targets in a multi-channel environment., • Strong workforce management skills: forecasting, scheduling, capacity planning and intraday management., • Experience running QA programmes and leading process improvement., • Experience leading remote teams., • Fluent English, strong Spanish preferred., • Right to work in Spain, and able to commute to Madrid once hybrid working begins (unconfirmed, no sooner than mid-2027)., • Zendesk or Talkdesk administrator certification., • Experience with dedicated WFM tools (e.g. Talkdesk WEM, Assembled, NICE, Calabrio)., • Experience using AI and automation in customer service including chatbots, AI agent assist, auto-routing., • Experience setting up or scaling a contact centre, or migrating between platforms. The role starts fully remote, working from within Spain. In late 2027 there may be an opportunity to step into a group-level role serving multiple tour operators, based at our Madrid office. Preference will be given to candidates who live in or are willing to relocate to the Madrid area. Working hours will follow the operation's service hours, with occasional cover for peaks or escalations. #J-18808-Ljbffr

Scope Ratings is seeking motivated analysts at various experience levels to join the Monitoring & Methodology team within Scope’s Structured Finance Ratings group. The Analyst role is ideal for analysts with 3 to 5 years of structured finance experience and a strong interest in surveillance, methodologies and models across all asset classes. Scope Ratings is seeking motivated analysts at various experience levels to join the Monitoring & Methodology team within Scope’s Structured Finance Ratings group. The Analyst role is ideal for analysts with 3 to 5 years of structured finance experience and a strong interest in surveillance, methodologies and models across all asset classes. You will play a key role in assessing the performance of rated transactions, developing analytical tools, supporting the ongoing enhancement of our rating methodologies, and contributing to high-quality credit research. This position offers a strong long‑term career path for high‑performing analysts, combining hands‑on analytical work in the structured finance domain with opportunities to deepen technical expertise in programming, modelling, and data analysis. • Conduct performance reviews of structured finance transactions and articulate credit opinions clearly, • Serve as a voting member in rating committees, • Contribute to updates of structured finance methodologies, • Develop and maintain internal analytical tools and automation scripts, • Prepare data extracts, dashboards, and presentations for monitoring and reporting, • Engage with issuers, arrangers, originators and investors during rating analyses, • Produce high-quality, insightful research and sector‑level commentary, • At least 3 years of experience in the structured finance sector or closely related sectors, • Independent thinker with strong written and oral communication skills, • Accountable, proactive, and able to work autonomously while managing multiple priorities, • Inquisitive and detail‑oriented, with strong commitment to data quality and consistency, • Strong ability to identify key risks, interpret data, understand complex transaction documentation, and form independent credit opinions, • Solid understanding of securitization structures, cash‑flow dynamics, workflows, and contractual and legal frameworks, • Proficiency with quantitative tools (e.g. cash flow modelling tools, statistical databases, data visualization tools) and MS Office computer skills (Word, Excel, PowerPoint) are highly valued., • Fluency in English, • Technical skills such as the following are a plus: programming (Python, R, VBA), Power BI dashboard development, databases (SQL, Databricks), cloud environments (Azure), version control tools (Git). Multiple location possible: Frankfurt, Berlin, Madrid, Milan. Pay Band: Analyst - Structured Finance Minimum: 61,000.00 EUR Maximum: 73,000.00 EUR Discretionary Scope offers an extensive range of benefits, please check our benefits page for more details. Please note: For non‑EU applicants, a valid work and residence permit is a prerequisite for this job position. Unfortunately, we are unable to sponsor relocation from outside of the EU at this time. Scope Ratings GmbH is part of the Scope Group with headquarters in Berlin and offices in Frankfurt, London, Madrid, Milan, Oslo and Paris. As the leading European credit rating agency, the company specialises in the analysis and ratings of financial institutions, corporates, structured finance, project finance and public finance. Scope Ratings’ credit risk analysis is opinion‑driven, forward‑looking and non‑mechanistic, an approach that adds to a greater diversity of opinion for institutional investors. Scope Ratings is a credit rating agency registered in accordance with the EU rating regulation and operating in the European Union with ECAI status. At Scope Group, we are committed to fostering a diverse and inclusive workplace where everyone is treated with respect and fairness. We embrace people from all backgrounds, regardless of culture, ethnicity and gender. We ensure that our application processes are free from discrimination. By valuing each individual's unique background and perspectives, we strive to create an environment where all employees can thrive and contribute their best. Our dedication to equality and inclusivity reflects our belief that diversity drives innovation and success. #J-18808-Ljbffr

MIO Group es un ecosistema integrado de talento especialista en estrategia de marketing, creación de activos digitales y activación de medios, orientada a aportar un impacto medible en la cuenta de resultados de sus clientes mediante el uso de la tecnología. Nuestro desarrollo ha venido de la mano de una estrategia de crecimiento orgánico e inorgánico, adquiriendo compañías con servicios o tecnologías diferenciales para incorporar y expandir su cartera de servicios para acabar así construyendo un líder nacional. MIO Group está compuesto por diferentes compañías altamente especializadas en distintos ámbitos del marketing y la publicidad: creatividad, compra de medios, analítica de datos, social media, desarrollo web, marketing automation y tecnología. Actualmente, el Grupo está formado por MIO One, SuperReal y Firma. ¿Quieres saber más de nosotros? Esta es nuestra web Beneficios de formar parte de nuestro grupo • Estabilidad, nos gustan las relaciones a largo plazo., • Maximiza el salario con nuestro Plan de Retribución Flexible., • Healthcare: Seguro médico a cargo de la compañía y fisioterapeuta en la oficina., • Teletrabajo: bolsa de días al mes para usar como mejor te venga y ampliación de éstos en periodos vacacionales., • Conciliación: jornada intensiva, horario flexible..., • Formación y plan de carrera individualizado, • Cultura y gran ambiente laboral Liderar la función de Research de la compañía, transformando datos de mercado, audiencia, consumo y negocio en conocimiento accionable que impulse la toma de decisiones estratégicas de clientes y equipos internos. Será el referente en inteligencia de mercado, metodologías de investigación y análisis de datos, asegurando la calidad de los insights y promoviendo una cultura data-driven en toda la organización. • Liderar la extracción, análisis e interpretación de información procedente de las principales fuentes del mercado (Kantar, EGM, InfoAdex, IOPE, GfK, Nielsen, Comscore, Similarweb, GWI y otras herramientas de investigación)., • Identificar tendencias de mercado, consumo, audiencias y competencia para generar oportunidades de negocio., • Elaborar informes de mercado, análisis sectoriales, benchmarkings y estudios ad hoc para clientes y equipos internos., • Convertir grandes volúmenes de datos en recomendaciones estratégicas claras y accionables., • Diseñar metodologías de investigación cuantitativa y cualitativa., • Definir objetivos, hipótesis, muestras y métricas de análisis., • Coordinar proveedores externos cuando sea necesario., • Garantizar la calidad metodológica de todos los estudios realizados., • Trabajar con grandes volúmenes de datos estructurados y no estructurados., • Diseñar procesos de limpieza, integración y explotación de datos., • Crear dashboards e indicadores de negocio mediante herramientas de Business Intelligence (Power BI, Tableau, Looker Studio o similares)., • Automatizar procesos de reporting siempre que sea posible., • Colaborar con los equipos de Estrategia, Comunicación, Marketing y Comercial para aportar evidencia y datos en la definición de propuestas y recomendaciones., • Participar en el desarrollo de propuestas para clientes aportando análisis de mercado e insights diferenciales., • Traducir resultados complejos en mensajes comprensibles para perfiles tanto técnicos como de negocio., • Elaborar informes ejecutivos, whitepapers, artículos y contenidos basados en datos., • Participar en presentaciones internas y externas., • Actuar como referente interno en materia de investigación y análisis., • Evaluar continuamente nuevas fuentes de datos, metodologías y herramientas de análisis., • Detectar oportunidades para incorporar Inteligencia Artificial y analítica avanzada en los procesos de investigación., • Impulsar la evolución del área de Research hacia modelos más predictivos y automatizados., • Experiencia en investigación de mercados, análisis de datos o inteligencia de negocio., • Dominio avanzado de herramientas de investigación de mercado (Kantar, EGM, InfoAdex, IOPE y similares)., • Nivel avanzado de PowerPoint para la elaboración de informes ejecutivos., • Experiencia trabajando con grandes volúmenes de datos., • Manejo avanzado de herramientas de Business Intelligence (Power BI, Tableau, Looker Studio o equivalentes)., • Capacidad para sintetizar información compleja y convertirla en insights de negocio., • Conocimientos de SQL., • Conocimientos de Python o R aplicados al análisis de datos., • Experiencia con IA aplicada a investigación y análisis., • Conocimiento de herramientas de visualización y automatización., • Experiencia en agencias de medios, consultoría o departamentos de estrategia. #J-18808-Ljbffr

A leading design firm in Madrid is seeking a Strategist to collaborate with designers and developers throughout the product lifecycle. This role involves conducting user research, formulating hypotheses, and presenting ideas to clients. The ideal candidate has strong storytelling and analytical skills, along with over a year of experience in the field. Familiarity with statistical software and an interest in technology are advantageous. This position requires the ability to communicate effectively in English and a willingness to travel for research and client meetings. #J-18808-Ljbffr

The Cocktail es una consultora tecnológica multinacional cuya misión es acelerar el crecimiento sostenible de nuestros clientes. Movilizamos grandes organizaciones para mejorar la relación entre las marcas y personas mediante el diseño, los datos y la tecnología. Entendemos lo que nuestros clientes necesitan y orquestamos capacidades para lograr esos objetivos a una velocidad de vértigo. Nuestra cultura se basa en la diversidad, creatividad y en la mezcla de especialistas (estrategia, diseño, tecnología, data, investigación…) Nuestras carreras se caracterizan por un crecimiento profesional exponencial, y por la participación en proyectos con impacto real en grandes clientes. Formar parte de The Cocktail implica rodearse de un equipo inspirador del que aprender y que te ayudará a crecer. Trabajamos bajo la máxima de que es mejor pedir perdón que permiso, por eso, esperamos de ti una visión disruptiva y challenger, inconformismo y pasión por la excelencia y los desafíos. Si quieres moverte en un entorno retador, crear proyectos innovadores y hacer que las cosas pasen, The Cocktail es para ti. Somos una consultora internacional referente en el mundo de la transformación digital. Trabajamos en proyectos endto end con nuestros clientes, desde que surge una necesidad hasta el desarrollo y la implementación de soluciones orientadas al impacto. Nos gusta entender a fondo el reto de cada proyecto y, con todo el talento que tenemos en casa, nos aseguramos de llevarlo a cabo con éxito. Personas con experiencia en la investigación cuantitativa ad-hoc con una decidida vocación y ganas de desarrollar su potencial en un entorno abierto a la creatividad y a la innovación tanto en técnicas como en enfoques. • Diseñarás investigaciones ad-hoc para grandes clientes de distintos sectores., • Desarrollarás proyectos de investigación cuantitativaend-to-end., • Participarás en: briefings y recogida de necesidades de clientes, definición de metodologías avanzadas e innovadoras, gestión integral de proyectos, presentación de informes y gestión de clientes., • Trabajarás en inglés, teniendo interlocución con diferentes países., • Gestionarás personas en contexto de proyecto, ayudando al crecimiento de otras personas del equipo., • Te sumergirás en el mundo de la transformación digital., • Ser referentedentro del equipo a nivel técnico., • +10 años de experienciacon historial comprobado liderando proyectos de investigación cuantitativaend-to-end(desde la toma de requerimientos hasta el análisis y presentación final) para grandes cuentas o marcas., • Experienciasque demuestren capacidad en metodologías complejas (ClusterizaciónMaxdiff,Conjoint, Ecuaciones estructurales, etc.) y su traducción ainsightsde negocio accionables, no solo entrega de datos., • Has tenido experiencia conSPSS, R o Pythony Excel avanzado. Se valora muy positivamente experiencia en herramientas de visualización de datos (PowerBI,Tableau) y conocimiento de herramientas de IA aplicadas al análisis y procesamiento de datos., • Liderazgo de pensamiento:punto de vista sólido, capacidad para elevar el dato a estrategia, construir unstorytellingconvincente y defender recomendaciones antestakeholdersde alto nivel., • Ambición de participar en proyectos internacionales y, por tanto, que te manejes perfectamente eninglés(imprescindible fluidez para presentaciones yreporting)., • Te adaptas bien en ambientes cambiantes y situaciones de incertidumbre, gestionando múltiples proyectos otimingsajustados con rigor metodológico., • Experiencia engestión y desarrollo de equipo(mentoringde perfiles Junior/Middle), pero que no se te caigan los anillos si hay que "bajar al barro" a revisar una tabulación, codificar o chequear un cuestionario., • Que seas curioso/a, que lacalidad del datoy la innovación metodológica sean tu objetivo constante., • Profesionalismo superior y presencia madura en todos los aspectos del trabajo, con mentalidad de consultoría y orientaciónacliente., • Modelo de trabajo basado en la autorresponsabilidad y la autogestión con horario flexible y teletrabajo., • 25 días de vacaciones al año., • Plan de carrera personalizado y formación continua., • No tenemos dress code. Ven como quieras a trabajar., • Descuentos exclusivos y tiempo para tu crecimiento., • Acceso a Cobee, el mejor sistema de retribución flexible., • Iniciativas de apoyo a la maternidad y políticas de igualdad y diversidad. WPP (The Cocktail/VML) es una empresa que ofrece igualdad de oportunidades y considera a los candidatos para todos los puestos sin discriminación ni consideración de características. Nos comprometemos a fomentar una cultura de respeto en la que todos se sientan parte de la empresa y tengan las mismas oportunidades de progresar en sus carreras. #J-18808-Ljbffr

BSBI's mission is to educate students to effectively shape the future and become excellent leaders of tomorrow in an ever-changing business world. It also aims to teach students to understand how businesses function and how economic success is generated. BSBI offers industry-relevant programs that focus on the development of practical entrepreneurial skills necessary for professional success. Located in the heart of Berlin and with campuses in Paris, Barcelona, Hamburg and Athens, we are an international business school that offers academic excellence, is a member of Global University Systems (GUS) and provides unlimited career opportunities for its students and staff. We are looking for a new colleague to join our team as a freelance lecturer in Global MBA with expertise in System Operations, Project Management and Leadership, starting July 2026. The Opportunity: The Freelance Lecturer at Berlin School of Business and Innovation (all campuses, all faculties) will be the principal academic contact and leader for the assigned Course/Unit/Module/Dissertation/Project/Internship. Please note that there is no differentiation in the standards or requirements of the tasks for Freelance or Full‑time faculty. The Freelance arrangement is just a mode of engagement to offer you greater flexibility. As a Freelance Lecturer, you will be requested to contribute to one or more of the following: A. Teaching B. Research Supervision C. Combination of Teaching and Research. RESPONSIBILITIES • Teaching in English and/or Spanish the assigned academic modules according to the curriculum., • Administering, proctoring and marking all students’ assignments and exam papers of all assigned classes., • Amending or designing and developing a new curriculum for a module, if required., • Updating a syllabus or syllabi, if required., • Supervising a number of dissertations per academic year (if required)., • Providing consultation and mentoring to students., • Creating assignment briefs and exam papers., • Providing feedback to students using positive reinforcement techniques to encourage, motivate or build confidence., • Teaching students study skills relevant to programmes and exam‑taking strategies., • Providing, if needed, private instruction to individual or small groups of students to improve academic performance and to prepare for exams., • Assessing students’ progress throughout tutoring sessions., • Scheduling tutoring appointments with students., • Monitoring student performance or assisting students in academic environments, such as classrooms, laboratories or computing centres., • Organising the tutoring environment to promote productivity and learning., • Participating in training and development sessions to improve tutoring practices or learn new tutoring techniques., • Communicating effectively with students and conveying passion for learning., • Maintaining records of students’ assessment results, progress, feedback or school performance, ensuring confidentiality of all records., • Preparing lesson plans or learning modules for tutoring sessions according to the programme’s needs and goals., • Creatively designing teaching materials that maximises students’ experience., • Developing content, both written and recorded, as directed by the Chief Academic Officer., • Researching or recommending textbooks, software, equipment or other learning materials to complement tutoring., • Communicating students’ progress to students in written progress reports, in person, by phone, by e‑mail and/or teleconferencing., • Identifying, developing or implementing intervention strategies, tutoring plans or individualised education plans (IEPs) for students., • Performing day‑to‑day tasks such as maintaining information files and processing paperwork related to teaching activities., • Providing feedback to students on their progress., • Playing a proactive role in promoting the school., • Providing all students with tutor support to develop their assignments., • Participating in the school’s activities as required by the Chief Academic Officer. PROFESSIONAL COMPETENCIES • PhD / PhDc or DBA / DBAc or MBA or Master’s Degree (in a business discipline), • Prior teaching experience in higher education at university level, • Very good knowledge of Windows OS, of MS Office suite (Excel, Word, Outlook, PowerPoint) and Microsoft Teams, • Scientific publications in a related discipline, • Fluent in spoken and written English (minimum 6.5 IELTS), • Fluent in Spanish, • Knowledge of educational platforms (i.e. Canvas, Blackboard etc.), • Working knowledge of timetabling software, • Sound knowledge of study regulations and rules PERSONAL COMPETENCIES • Very good organisational and communication skills, • High social competence and assertiveness, • Maintaining an overview even with high workloads, • Entrepreneurial and economic way of thinking and working, • Resilient and flexible, • Motivated for further academic and professional development BSBI’s mission is to educate students to effectively shape the future and become excellent leaders of tomorrow in an ever‑changing business world. It also aims to teach students to understand how businesses function and how economic success is generated. BSBI offers industry‑relevant programmes that focus on the development of practical entrepreneurial skills necessary for professional success. Located in the heart of Berlin, we are an international business school that offers academic excellence. We are a member of Global University Systems (GUS) and provide unlimited career opportunities for its students and staff. #J-18808-Ljbffr

CUNEF Universidad in Madrid invites applications for a tenure-track Assistant Professor of Accounting, starting September 2027. The position offers a dynamic, international, and research-oriented environment with access to research data and funding, and a highly competitive salary and benefits package. Responsibilities include conducting high-quality research and publishing in leading journals, teaching undergraduate and graduate courses, and contributing to the intellectual life of the #J-18808-Ljbffr

Select how often (in days) to receive an alert: Welcome to the future of nuclear energy, where Westinghouse Electric Company is leading the field with expertise and innovation to shape the power of tomorrow. At Westinghouse, innovation is in our DNA. We are creative. We think differently. We reimagine the possible across the nuclear industry every day. As a Senior I&C instructor you will you will help deliver high-quality technical training programs focused on Instrumentation & Control systems for nuclear power plants. You will combine your technical expertise in teaching to develop training materials and deliver engaging classroom, laboratory, and practical training sessions. You will be part of a global I&C Training team, working with colleagues in both Spain and the United States to ensure training programs reflect operational needs, industry best practices. This is a full-time job with a hybrid mode with a mix of on-site and remote work. You will report to the Operations and Technical Training Managerand be located at our HQ in San Sebastián de los Reyes. • Develop and review technical training materials for Instrumentation & Control systems., • Support the digitalization of training programs by providing technical expertise for the development and adaptation of instructional content to new learning platforms and digital training tools., • Deliver classroom, laboratory, and practical training sessions to internal and external audiences., • Prepare, administer, and evaluate examinations and trainee performance., • Apply adult learning principles instructional techniques to enhance knowledge retention and engagement., • Incorporate operating experience, lessons learned, and industry best practices into training programs., • Maintain training records and documentation within learning management systems., • Collaborate with engineering, operations, and project teams to ensure technical accuracy of training content., • Support qualification programs and workforce development plans., • Contribute to the continuous improvement of training materials, methods, and processes., • Provide technical support to company partners and customers., • Technical degree or Bachelor's degree in Engineering, Instrumentation & Control, Electrical Engineering, Electronics, or a related technical discipline., • Minimum of 7 years of experience in Instrumentation & Control, plant operations, maintenance, engineering, commissioning, or related industrial environments., • Knowledge of Instrumentation & Control systems and industrial processes., • Experience in technical training, technical documentation, or knowledge transfer activities., • Commitment to safety, quality, and continuous improvement., • Experience with teaching and developing technical talent., • Customer-focused mindset and collaborative approach., • Availability for occasional international travel. #LI-Hybrid We know that to put forth your best effort, you need to be challenged and enjoy what you do in a supportive and respectful environment. We aim to maintain this balance by offering our employees the amenities, benefits and training they need to reach personal and professional goals. Below is an example of what employees in Spain can expect: • Attractive remuneration, • Hybrid model of work., • High flexibility and autonomy., • Great benefits for your convenience and safety:, • Peer-to-peer recognition program., • Lunch allowance., • Private health insurance, • Employee Assistance Program: confidential counseling and resources for employees, eligible dependents, and household members, • Learning and development opportunities., • We encourage our employees to participate in community service events and other team-building activities to strengthen their bonds and inspire each other. Westinghouse is an Equal Opportunity Employer including Veterans and Individuals with Disabilities. #J-18808-Ljbffr

London, United Kingdom Budapest, Hungary Reading, Berkshire, United Kingdom Bloemfontein, South Africa Dublin, Ireland Centurion, South Africa Barcelona, Spain Sofia, Bulgaria Madrid, Spain Full time R This unique role within IQVIA lends itself to a Lead programmer on Cluepoints called Centralized Monitoring Analyst (CMA) with strong communication and organisation skills. Having experience with SAS programming is necessary. This role is part of a sponsor dedicated project where you will be working with the client directly to manage deliveries. The CMA contributes to the execution of the Centralized Monitoring process by performing the setup, programming and refresh(es) of the Centralized Monitoring platform, according to the study-specific Centralized Monitoring Plan (CMP). • Supports the Centralized Monitoring Lead (CML) in the development of the fit-for purpose CM strategy by contributing to the identification of the relevant CM elements to be implemented for the study (Quality Tolerance Limits (QTL), Key Risk Indicators, data visualizations and Data Quality Assessments), • Setup/Program QTL, KRI and Data Quality Assessments according to the study CMP, • Refresh the Centralized Monitoring Platform at predefined frequency to enable signal identification, • Generate and maintain the Centralized Monitoring Platform specifications document and file it in eTMF, • Review and understanding of protocol is key, • Understand the data sources for the study, the data transfer specifications and the data structure, • Execute and document peer-review of CM platform setup done by other CMA colleagues, • At least 3 years relevant experience in the area of pharmaceutical research and development or related field preferably in centralized Monitoring, data management, and/or biostatistics, • 2-3 years SAS experience including macro language, • Knowledge/ experience working on Cluepoints, • Ability to work in an autonomous way and engage with relevant stakeholders to execute activities related to study level centralized monitoring process., • Ability to understand basic statistical analysis concepts and to interpret their outcome., • Ability to maintain confidentiality of data and information during interactions with staff at all levels, • Ability to work with limited close supervision., • Demonstrated communication, interpersonal, organizational and problem-solving skills, • High levels of initiative, drive and commitment., • Prior experience in a Data Management related field is required, • Experience with relational databases, preferably Clinical Data Management and EDC Systems, • Experience communicating with all levels of personnel and participating in collaborative work team (locally and globally)., • Advanced knowledge of federal regulations, Good Clinical Practice, and Good Clinical Data Management Practices., • Excellent command, both verbal and written, of English This role is not eligible for UK visa sponsorship #J-18808-Ljbffr

Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need. Discover what your 25,000 future colleagues already know: • We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program., • We are committed to building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life., • We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress. Responsible for the quality deliverables at the country level; follows project requirements and aapplicable country rules with moderate oversight from the SSU Country Manager. Works within the forecasted submission/approval timelines and ensures they are complied with and tracks milestone progress in agreed upon SSU tracking system in real time; if forecasted timelines are not reached: investigates and provides clear rationale for delays, provides support on contingency plan to mitigate impact, and escalates the issue as soon as identified. Monitors basic financial aspects of the project and the number of hours/tasks available per contract; escalates discrepancies in a timely fashion. Reviews and complies with Standard Operating Procedures (SOPs) and Work Instructions (WI) in a timely manner, keeps training records updated accordingly and ensures timesheet compliance. Supports continuous improvement of quality in all Site Start-Up (SSU) components at the country level where assigned (submissions, essential document collection, communication to Competent Authorities and ECs, etc.). Ensure all relevant documents are submitted to the Trial Master File (TMF) as per Company SOP/Sponsor requirements. Responsible for the Local Submissions Specialist - Follows the project direction provided by the designated country start-up advisor (CSA) and SAM. May serve as a point of contact for the PM/SAM (or designee) during start-up on allocated projects. Complies and/or reviews essential document packages for site activation and may also be involved in essential document collection from site. Prepares and submits Central EC Applications, Local EC Applications, RA Applications, and other local regulatory authorities or hospital approval submissions as required. Prepares ongoing submissions, amendments, and periodic notifications required by central and local EC and RA and other local regulatory authorities as needed within the country; includes safety notifications as required by local rules, with moderate oversight from the SSU Country Manager. May act as liaison and facilitator between investigational sites and functional leads for related tasks and/or issues. Oversee site activation end to end process at country/ site level. Country Start-Up Advisor - Acts as Subject Matter Advisor for in-country performance within the Site Start-Up. Supports country-level intelligence on start-up (SU) and clinical trial regulatory (CTR). Ensures that local country regulatory intelligence, as it pertains to the activities of the local SU and CTR team, is maintained on the central repository, e.g., Competent Authority submissions, EC submissions, notifications to data protection authorities, notifications/applications to any other local/federal/national body, and import/export license applications where these are obtained with RA applications. In absence of legal advisor or dedicated subject matter may provide support for data protection at the country and provide guidance at a country level on data protection statements that need to be included on those documents which the Sponsor has contracted to the Company start-up group to adapt to local requirements. This may include the Principal Investigator/Informed Consent and the Confidential Disclosure Agreement/contract template. Provides input in local SOPs and WI. Supports the creation of internal training materials on local legislation requirements. Provides input to the team to assist with EC or CA issue resolution at the country level. Local Site ID and Feasibility Support – Provides support with site selection lead and PM/SAM to ensure that the appropriate sites are selected for individual studies based on the requirements of the clinical trial. Qualifications Bachelor’s Degree, Over 2 years of experience on the role. Detailed understanding of clinical trial process across Phases II-IV and ICH GCP. Ability to understand clinical protocols and associated study specifications. Detailed understanding of clinical trial start-up processes. Ability to manage external vendors to contract effectively. Strong organizational skills with ability to handle multiple tasks effectively. Strong written and verbal communication and interpersonal skills. Ability to manage multiple project budgets with increased complexity and value. Quality-driven in all managed activities. Good negotiating skills. Good problem-solving skills. Demonstrated ability to work independently as well as part of a team. Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. #J-18808-Ljbffr

osapiens is seeking a Team Lead, Customer Success in Madrid to lead a 6–8 member CS team and personally manage a small portfolio of strategic accounts (~25% of time). You will drive retention and expansion, escalate effectively, train the team, and shape renewal processes while collaborating with Sales, Product, Support, and Engineering. You will build a high-performing, consultative CS function, balancing hands-on work with leadership, and work from our Madrid office with up to 2 days home #J-18808-Ljbffr

IQVIA seeks a Clinical Monitoring Analyst (Cluepoints) to lead setup and programming of centralized monitoring using Cluepoints with SAS macros. The role supports a sponsor-dedicated project and requires strong communication across global teams. You will interpret study CMPs, coordinate CM activities, and ensure CM deliverables align with protocol and regulatory standards. Remote flexibility offered. #J-18808-Ljbffr

AbbVie seeks an experienced Senior/Global Site Management leader to direct CSM integrity, quality, and timeliness across assigned studies. You will shape the study-level CSM strategy and collaborate with global and country teams to drive site activation, engagement, and close-out, ensuring regulatory readiness. You will manage resources, monitor risk, and maintain TMF artifacts, with a focus on cross-functional leadership in a matrix environment and fluency in English to communicate with global #J-18808-Ljbffr

RESEARCH ANALYST BUSINESS EXECUTIONSolicitarremote type: Hybridlocations: 28050, MADRID, Madridtime type: Full timeposted on: Publicado hoytime left to apply: Fecha final: 24 de julio de 2026 (Quedan 17 días para realizar la solicitud)job requisition id: JR00108153¿Te entusiasma hacer crecer tu carrera?BBVA es una compañía global con más de 160 años de historia que opera en más de 25 países donde damos servicio a más de 80 millones de clientes. Somos más de 121.000 profesionales trabajando en equipos multidisciplinares con perfiles tan diversos como financieros, expertos legales, científicos de datos, desarrolladores, ingenieros y diseñadores.Conoce más sobre el área:BBVA Research es el área de estudios económicos de BBVA. Analiza y hace previsiones sobre las principales tendencias económicas, financieras, digitales y geopolíticas a nivel mundial, así como sus implicaciones en la evolución macro y microeconómica y en los sistemas financieros de los países de interés para BBVA, sobre todo aquellos en los que tiene presencia. Asimismo, BBVA Research elabora informes sobre estos temas de análisis para su difusión publica, y mantiene un dialogo permanente con los responsables de política económica en línea con su labor investigadora. BBVA Research busca permanentemente la excelencia en el análisis económico, que se logra con el empleo de herramientas analíticas de última generación, como la econometría y el análisis de Big Data.Sobre el puestoBuscamos un/una economista o científico de datos con sólida formación cuantitativa y experiencia en técnicas de Big Data y conocimientos en economía. El trabajo consistirá en participar en proyectos de Big Data explotando los datos BBVA Data para el análisis y desarrollo de indicadores Macroeconómicos y participación en Proyectos Internacionales junto a Universidades Internacionales, Organismos Públicos (Bancos Centrales y Ministerios) y Organismos Internacionales.Otra parte muy relevante del trabajo consiste en proyectos de Análisis Económico, Social y Geopolítico explotando y procesando Información No Estructurada (texto) y técnicas de Procesamiento de Lenguaje Natural incluyendo Grandes Modelos de Lenguaje (LLM). Habrá una fuerte colaboración con los países donde BBVA opera.Las tareas asociadas a esta posición consisten principalmente en: Colaborar en proyectos de Big Data, desde el tratamiento de los datos, análisis de los mismos y diseño del producto final, proyectos end-to-end. Desarrollar herramientas de análisis cuantitativo en el ámbito económico, social y geopolítico. Profundizar en el uso de los datos de BBVA para el análisis económico. Participar activamente en los proyectos, presentaciones e informes de la Unidad.* Colaborar activamente con los países del BBVA y dar soporte a ambas unidades en proyectos de Big Data y de IA y LLM.Cualificaciones necesarias: Grado en Economía/Ciencia de Datos y estudios de Máster / Postgrado Conocimientos de análisis macroeconómico y econométrico Conocimientos en ciencia de datos, con manejo de SQL, Python, PySpark Conocimiento en NLP (procesamiento de lenguaje natural) y LLM (grandes modelos de lenguaje) Dominio del inglés (oral y escrito) Buenas dotes de comunicación* LiderazgoHabilidades:Empatía, Ética, Innovación, Orientación al cliente, Pensamiento proactivo #J-18808-Ljbffr

NeXT Consultans in Madrid is seeking an International and Institutional Liaison Officer to lead the integration of scientific strategies and manage the Centre's research dissemination. The successful candidate will possess extensive project management experience, expertise in international communication, and a strong background in coordinating dissemination activities. This position offers access to advanced technologies and integration into a prominent research environment. #J-18808-Ljbffr

Syneos Health is seeking a Site Activation Specialist II for Madrid, operating in a hybrid model within our Clinical Solutions team. The role focuses on coordinating country-level site activation activities, ensuring timely submissions and adherence to SOPs. You will manage local EC/RA submissions, liaise with investigators and vendors, and support country startup processes from start-up through activation, contributing to high-quality regulatory deliverables and timelines. #J-18808-Ljbffr

IE University invites applications for the position of Associate Dean for Faculty and Research at the IE School of Architecture and Design, located in Segovia and Madrid, Spain. The Associate Dean will guide the school’s research strategy, mentor faculty, and support promotion and tenure decisions while fostering cross-disciplinary collaboration across campus. The successful candidate will be an internationally respected scholar with a strong track record in research leadership, external #J-18808-Ljbffr

At Ayvens, progress starts with you. Our ambitions to shape the future of sustainable mobility are powered by our talent. Join us, and get better with every move. At Ayvens, progress starts with you. Our ambitions to shape the future of sustainable mobility are powered by our talent. Join us, and get better with every move. At Ayvens we have an opening for an User Researcher As our User Researcher, you will be responsible for driving user-centered decision making across our digital products by planning, executing, and communicating high-quality research that informs design and product strategy. • Planning and conducting qualitative and quantitative user research across the product lifecycle, • Translating research findings into clear, actionable insights for product and design teams, • Collaborating closely with product managers, designers, and engineers to shape product direction and vision, • Selecting appropriate research methods (e.g. interviews, usability testing, surveys, analytics) based on research questions, • Creating and maintaining research documentation, repositories, and insight tracking, • Advocating for user needs and embedding a user-centered mindset across the organization, • Supporting and mentoring designers and product teams in conducting lightweight research The ideal candidate has the experience and interpersonal skills necessary to gather user insights, translate these into meaningful product improvements and effectively collaborate across teams and geographies. Aside from being a skilled researcher, you are curious, proactive, and passionate about understanding user behavior. You will have relevant experience in a similar role, holding a Bachelor’s or Master’s degree in Human-Computer Interaction, Psychology, Design, or a related field. • 3–5 years of experience in user research within a multi-domain digital product environment, • Strong expertise in both qualitative and quantitative research methods, with the ability to effectively plan and execute studies, • Ability to clearly communicate insights and influence stakeholders up to C-level, • Experience working in cross-functional product teams, • Familiarity with research tools and platforms (e.g. UserTesting, Hotjar, Matomo, Google Analytics), • Strong organizational skills and ability to manage multiple research projects simultaneously, • Comfortable working in an international, collaborative environment, • Fluent in English is required. We’re on this journey together. By investing in professional growth, rewards and incentives, plus plenty of training and experience on the job, we create an inspiring environment for our colleagues that fosters high performance with positive impact. We believe in rewarding you holistically, through compensation, competitive benefits and rich development opportunities. We enable you to reach your full potential by offering you the opportunities and support to reach the next level in your career. We offer a wide variety of benefits to help keep you mentally and physically strong and to find the perfect work–life balance. We create an engaging environment where you can be your authentic self and harness your commitment, curiosity and collaboration. We’re conscious of our environment and the societies we’re part of and we work together to drive electrification and lead the way to decarbonisation. Ayvens provides a unique opportunity: the chance to accelerate the transition to electric, lead the way to decarbonisation and shape the industry’s digital transformation. Behind the wheel, our people make the difference, driving us towards our ambitions. Ayvens is home to the best talent in the industry – so if you’re looking for a fulfilling career with positive impact, we’d love to discuss your opportunities with us! Join a global leader in sustainable mobilityand follow @ayvens, @lifeatayvens, and Ayvens on LinkedIn to check out what’s happening at Ayvens! We’re committed to building a culture where everyone can be themselves and where everyone gets an equal chance to make their journey count. If you’d like to learn more about our DE&I journey – and how you can contribute – please find out more on Career pages of our website. With over 3.1 million vehicles managed across more than 40 countries, we provide full-service leasing, flexible subscription services, fleet management services and multi-mobility solutions to customers of all sizes, including large corporates, SMEs, professionals, and private individuals. By leveraging our unique position to lead the way to net zero and further shape the digital transformation of the industry, we are well-positioned to meet the evolving mobility needs of our clients and provide them with the solutions they need to thrive. At Ayvens, we believe that our success is driven by our commitment to customer satisfaction. Our team is dedicated to delivering innovative solutions and technology-enabled services that help our customers focus on their everyday business. We’re committed to sustainable mobility and have made it a core part of our strategy. In everything we do, we’re guided by the principles of authenticity, curiosity, commitment and collaboration. We aim to foster an organisation that's diverse in people and ideas, where everyone can thrive and be themselves, no matter who they are. Join us on this exciting journey as we continue to enable the transformation towards large scale adoption of sustainable mobility and provide our customers with the solutions they need to succeed. Follow our page for the latest updates, news, and insights. #J-18808-Ljbffr

Location in Madrid. FSP. Hybrid model. Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need. Discover what you 25,000 future colleagues already know: • We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program., • We are committed to building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life., • We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress., • Responsible for the quality deliverables at the country level; follows project requirements and aapplicable country rules with moderate oversight from the SSU Country Manager. Works within the forecasted submission/approval timelines and ensures they are complied with and tracks milestone progress in agreed upon SSU tracking system in real time; if forecasted timelines are not reached: investigates and provides clear rationale for delays, provides support on contingency plan to mitigate impact, and escalates the issue as soon as identified., • Monitors basic financial aspects of the project and the number of hours/tasks available per contract; escalates discrepancies in a timely fashion., • Reviews and complies with Standard Operating Procedures (SOPs) and Work Instructions (WI) in a timely manner, keeps training records updated accordingly and ensures timesheet compliance., • Supports continuous improvement of quality in all Site Start-Up (SSU) components at the country level where assigned (submissions, essential document collection, communication to Competent Authorities and ECs, etc.)., • Ensure all relevant documents are submitted to the Trial Master File (TMF) as per Company SOP/Sponsor requirements., • Responsible for the Local Submissions Specialist - Follows the project direction provided by the designated country start-up advisor (CSA) and SAM. May serve as a point of contact for the PM/SAM (or designee) during start-up on allocated projects. Complies and/or reviews essential document packages for site activation and may also be involved in essential document collection from site. Prepares and submits Central EC Applications, Local EC Applications, RA Applications, and other local regulatory authorities or hospital approval submissions as required. Prepares ongoing submissions, amendments, and periodic notifications required by central and local EC and RA and other local regulatory authorities as needed within the country; includes safety notifications as required by local rules, with moderate oversight from the SSU Country Manager., • May act as liaison and facilitator between investigational sites and functional leads for related tasks and/or issues. Oversee site activation end to end process at country/ site level., • Country Start-Up Advisor - Acts as Subject Matter Advisor for in-country performance within the Site Start-Up. Supports country-level intelligence on start-up (SU) and clinical trial regulatory (CTR). Ensures that local country regulatory intelligence, as it pertains to the activities of the local SU and CTR team, is maintained on the central repository, e.g., Competent Authority submissions, EC submissions, notifications to data protection authorities, notifications/applications to any other local/federal/national body, and import/export license applications where these are obtained with RA applications. In absence of legal advisor or dedicated subject matter may provide support for data protection at the country and provide guidance at a country level on data protection statements that need to be included on those documents which the Sponsor has contracted to the Company start-up group to adapt to local requirements. This may include the Principal Investigator/Informed Consent and the Confidential Disclosure Agreement/contract template. Provides input in local SOPs and WI. Supports the creation of internal training materials on local legislation requirements. Provides input to the team to assist with EC or CA issue resolution at the country level. Local Site ID and Feasibility Support – Provides support with site selection lead and PM/SAM to ensure that the appropriate sites are selected for individual studies based on the requirements of the clinical trial. • May be asked to perform: Local Investigator Contract and Budget Negotiator – Provides support to SAM to agree on country template contract and budget. Produces site-specific contracts from country template. Provide support in submissions for proposed contract and budget for site. Provides support in negotiating budget and contract with site via Site Contracts Service Centre and SAM with Sponsor until resolution of issues and contract execution. Performs quality control and arranges execution of CTAs as well as archival of documents into repositories and capture of metadata., • Bachelor’s Degree,, • Over 2 years of experience on the role., • Detailed understanding of clinical trial process across Phases II-IV and ICH GCP., • Ability to understand clinical protocols and associated study specifications., • Detailed understanding of clinical trial start-up processes., • Ability to manage external vendors to contract effectively., • Strong organizational skills with ability to handle multiple tasks effectively., • Strong written and verbal communication and interpersonal skills., • Ability to manage multiple project budgets with increased complexity and value., • Quality-driven in all managed activities., • Good negotiating skills., • Good problem-solving skills., • Demonstrated ability to work independently as well as part of a team. Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. #J-18808-Ljbffr

IE University in Madrid and Segovia, Spain, invites applications for scholars in political science, international relations, and related fields. The successful candidates will join SPEGA within the Political Science and International Relations group, with a strong record of empirical work and a focus on comparative politics, international relations, political economy, and political behavior. The department offers a competitive remuneration package, teaching commitments, and an English-working #J-18808-Ljbffr

BYD Group is a leading, high-tech multinational company based in Shenzhen, China. Operating in four core fields: IT, automotive, new energy, and rail transit, BYD employs over 300,000 people worldwide. At BYD Iberia, we are redefining the future of mobility. As part of the world's leading New Energy Vehicle company, we are committed to building a sustainable, zero-emission future where technology and nature coexist in harmony. Your mission is to strengthen BYD’s brand presence and accelerate its growth in the Spanish market by developing and executing impactful ATL media campaigns and brand activations. You will maximise media investment, increase brand awareness and consideration, and create engaging brand experiences that support vehicle launches, drive consumer engagement and contribute to business results. You will lead the planning, negotiation and execution of integrated Above-the-Line (ATL) marketing campaigns across TV, radio and audio, out-of-home (OOH), print, sponsorships and special media formats. You will manage media plans and budgets, negotiate with media owners and suppliers, monitor campaign performance and identify opportunities to maximise media investment and effectiveness. You will also coordinate brand activations and events, collaborating with internal teams, creative agencies, media partners and other stakeholders to ensure consistent brand communication across all customer touchpoints. In addition, you will analyse campaign results, prepare reports and dashboards, provide actionable recommendations and ensure all marketing activities comply with Spanish advertising regulations and brand guidelines. • University degree in Marketing, Communications, Business or a related discipline., • At least 5 years’ experience planning and delivering ATL media campaigns., • Experience across TV, OOH and radio or audio; print and event experience are an advantage., • Strong understanding of the Spanish media landscape and proven experience negotiating directly with media owners., • Experience managing budgets, media plans, campaign delivery and performance reporting., • Strong analytical skills and the ability to turn results into practical recommendations., • Knowledge of Spanish advertising regulation and self-regulation (Autocontrol), ideally in the automotive sector., • Familiarity with Spanish audience and investment measurement sources (Kantar, EGM/AIMC, Geomex, Infoadex) is a plus., • Native or C2-level Spanish, with excellent written and verbal communication skills in English., • Strong presentation skills and excellent working knowledge of Microsoft Office., • Able to manage priorities, deadlines and several projects at once., • Proactive, resilient, collaborative and results-oriented, with a hands-on approach., • Join a fast-growing company and industry that represents sustainable technology and innovation., • Competitive remuneration package based on experience and performance, including commuting allowance., • Team-building activities and continuous learning opportunities., • Supportive and inclusive work culture., • Opportunities for career growth and professional development., • Cross-national training: Participate in training sessions across various countries, gaining valuable global insights and experience. Our Purpose is to build a zero-emission future that reconnects humanity with nature and creates a world of clean air. We are looking for talented individuals who connect with this mission and want to create a positive impact by joining a diverse and dynamic team #J-18808-Ljbffr

Mercor connects elite creative and technical talent with leading AI research labs. Headquartered in San Francisco, our investors include Benchmark, General Catalyst, Peter Thiel, Adam D'Angelo, Larry Summers, and Jack Dorsey. Position: Music & Lyrics Expert - Spanish (ES) Type: Contract Compensation: $39–$54/hour Location: Remote Duration: Up to 6 months Commitment: 20+ hours/week Role Responsibilities • Evaluate AI-generated music across various genres. Rate against detailed quality standards in Spanish (ES) and English., • Compare AI-generated lyrics with published songs. Identify similarities and differences., • Rate lyrics on quality, creativity, prompt adherence, and originality., • Assess lyrics for naturalness, including word choice, slang, and regional expressions., • Work independently with flexible hours to meet project goals. Qualifications Must-Have • Native or near-native proficiency in Spanish (ES). Ability to follow detailed instructions in English., • Experience as a songwriter, lyricist, performer, composer, or music journalist. Knowledge of the Spanish (ES) music scene., • Headphones or studio monitors suitable for critical listening. Preferred • Formal training in music performance, theory, or composition., • Credited or published songwriting work., • Broad familiarity with contemporary Spanish (ES) genres, sub-genres, and artists. Start Date • Immediate #J-18808-Ljbffr

Scope Ratings GmbH seeks analysts to join the Monitoring & Methodology team in Structured Finance Ratings. The role targets candidates with 3–5 years in structured finance and a strong interest in surveillance, methodologies and models across asset classes. You will assess rated transactions, build analytical tools, and support ongoing methodological enhancements with opportunities to deepen programming and data analysis skills. #J-18808-Ljbffr

Travel: Availability to travel across Europe and internationally when required Want to know more? The successful candidate will play a key role in study execution, working closely with investigators, study coordinators, internal teams and other stakeholders to ensure data quality, patient safety, protocol compliance and the successful delivery of clinical trials within agreed timelines . We are looking for someone with strong clinical monitoring experience, a high level of autonomy, a risk-based mindset and a strong commitment to quality and continuous improvement. If you are motivated by taking ownership, working in an international environment and contributing directly to the successful delivery of clinical trials, we would love to hear from you . As a Senior CRA , you will be responsible for the management and oversight of assigned clinical trial sites throughout the different stages of the study. Your key responsibilities will include: • Independently manage assigned clinical trial sites throughout the study lifecycle., • Conduct site initiation, routine monitoring and close-out visits in accordance with the monitoring plan, study timelines and regulatory requirements., • Review source documentation, CRFs and site records to verify accuracy, completeness and protocol compliance., • Ensure essential study documentation is complete, up to date, accurate and inspection-ready., • Verify that informed consent is obtained and documented appropriately in accordance with the protocol, ICH-GCP and applicable regulations., • Identify, assess and manage site issues, protocol deviations and operational risks., • Drive the timely follow-up and resolution of issues and action items., • Prepare accurate, clear and timely monitoring visit reports and follow-up letters., • Review clinical and regulatory documentation to ensure consistency, completeness and quality., • Support data review and query resolution in collaboration with sites and study teams., • Act as the primary point of contact for assigned sites., • Maintain effective communication with investigators, study coordinators and site staff., • Advise sites on protocol requirements, study procedures, investigational product accountability and GCP requirements., • Work closely with Clinical Operations, Data Management, Medical, Regulatory and other cross-functional teams., • Proactively elevate significant site risks, quality concerns and relevant operational issues., • Contribute to study-level operational discussions and planning related to site management and trial execution., • Ensure compliance with ICH-GCP, corporate SOPs, study protocols and applicable local and international regulations ., • Drive site-level inspection readiness through proactive oversight of documentation, processes and outstanding actions., • Protect the rights, safety and well-being of clinical trial participants throughout the study., • Provide guidance and support to junior or less experienced CRAs and contribute to onboarding, training and knowledge-sharing initiatives., • Share best practices and lessons learned across the Clinical Operations team., • Contribute to overall study development through effective site-level leadership, risk management and cross-functional collaboration. We are looking for a strong clinical research professional who brings solid monitoring experience, operational leadership and a quality-focused mindset. • Bachelor's or Master's degree in Life Sciences, Pharmacy, Chemistry, Medicine, Nursing, Biotechnology or another relevant scientific discipline., • Additional certifications or qualifications will be considered a plus., • At least 5 years of experience in clinical research , including clinical trial monitoring and independent site management., • Experience within the pharmaceutical, biotechnology, CRO/service provider or healthcare sector., • Experience managing complex sites, operational issues and escalated situations., • Strong knowledge of ICH-GCP , applicable clinical research regulations and monitoring practices., • Solid understanding of clinical trial processes, site management, monitoring activities and essential study documentation., • Proven ability to identify, assess and manage complex site issues, protocol deviations and operational risks., • Knowledge of site-level quality standards and inspection readiness ., • Experience applying a risk-based oversight approach, with strong prioritisation and escalation skills., • Native-level French is required., • Fluent English , both written and spoken., • Additional European languages will be considered a plus., • Excellent communication and interpersonal skills., • Strong organisational, prioritisation and problem-solving abilities., • High level of autonomy and ability to make sound decisions in a dynamic environment., • Strong ability to collaborate with multidisciplinary and international teams., • Ability to coach and support junior or less experienced CRA profiles., • Good knowledge of Microsoft Office and clinical trial systems., • Strong reporting skills and attention to detail, with the ability to maintain accurate and well-organised study records., • Willingness and availability to travel across Europe and internationally when required . You will have the opportunity to work in an international environment, collaborate with multidisciplinary teams and contribute to clinical trials where your expertise can have a direct impact on study quality and execution. We are looking for people who want to continue growing, take on meaningful challenges and contribute to the advancement of clinical research. At CROVELIS , we are committed to fostering a diverse, inclusive and equal-opportunity workplace. All applications will be considered regardless of gender, gender identity or expression, age, ethnicity, nationality, religion, sexual orientation, disability or any other personal, physical or social condition. We are committed to ensuring fair and non-discriminatory recruitment processes. #J-18808-Ljbffr

Precision for Medicine in Spain seeks a Senior Clinical Research Associate to support a dedicated FSP partnership with a strategic sponsor in a highly collaborative and quality-focused environment. This evergreen posting allows consideration for future opportunities; role can be fully home-based within Spain with up to 50-60% travel for site monitoring and related activities. Fluency in Spanish and English is required. #J-18808-Ljbffr

A leading clinical research organization is looking for a Senior Clinical Research Associate in Madrid. The successful candidate will oversee clinical trial activities ensuring compliance with protocols and regulatory standards. Key responsibilities include monitoring trial sites, conducting visits for performance assessment, and ensuring data integrity. Candidates should have relevant advanced degrees and extensive CRA experience. This role offers competitive salary and comprehensive benefits aimed at promoting well-being and work-life balance. #J-18808-Ljbffr

Garaje de ideas busca un/a Senior UX Researcher con autonomía para definir y ejecutar investigación end-to-end en productos digitales complejos (B2B/Enterprise), transformando hallazgos en acciones para producto y diseño.Definirás objetivos, hipótesis y criterios de selección; realizarás entrevistas,pruebas de usabilidad y análisis de workflows; crearás journeys, personas y dashboards para comunicar recomendaciones respaldadas por evidencia, con foco en ética y privacidad de datos.#J-18808-Ljbffr

Garaje de ideas busca un Senior UX Researcher con autonomía para definir y ejecutar investigaciones end-to-end en productos digitales complejos B2B/Enterprise. El objetivo es entender necesidades, flujos y contextos de uso y convertir hallazgos en recomendaciones accionables que conecten con estrategia de producto. Trabajarás con equipos de producto y diseño, liderando entrevistas, pruebas de usabilidad, análisis de workflows y la definición de journeys, personas y dashboards para respaldar #J-18808-Ljbffr

IQVIA is the Human Data Science Company oriented to drive human health outcomes forward. When you join IQVIA Spain as a sponsor-dedicated CRA, you’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our customers. With access to world-class training and mentoring, you’ll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas. • Performing site selection, initiation, monitoring and close-out visits, • Supporting the development of a subject recruitment plan, • Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines, • Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution, • Collaborating with experts at study sites and with client representatives, • University degree in scientific discipline or health care, • At least 2 years of on-site monitoring experience, • Good knowledge of clinical research regulatory requirements, • Very good computer skills including MS Office, • Excellent command of Spanish and English language, • Organizational, time management and problem-solving skills, • Ability to establish and maintain effective working relationships with coworkers, managers, and clients, • Flexibility to travel, • Driver’s license class B, • Resources that promote your career growth, • Leaders that support flexible work schedules, • Programs to help you build your therapeutic knowledge, • Better Work-Life balance, optimal DOS, • Excellent working environment in a stabile, international, reputable company, • Mobile phone and attractive benefits package IQVIA 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 IQVIA 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. At 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. #J-18808-Ljbffr

A leading AI research firm in Spain seeks an experienced AI Research Engineer to advance large-scale pre-training systems. You will work directly with cutting-edge GPU architectures to design training pipelines and improve model performance. Ideal candidates have a PhD in Computer Science or related fields, hands-on experience in LLM pre-training, and strong collaboration skills. Enjoy a competitive compensation package and a remote-friendly work environment focused on frontier AI research. #J-18808-Ljbffr

EURAXESS Ireland is seeking a Principal Research Engineer in Applied Cybersecurity and Intelligent Systems in Madrid. The role involves leading R&D projects and managing cybersecurity initiatives focused on AI integration. Candidates should hold a relevant Bachelor’s and Master’s degree, with a PhD valued highly. A minimum of five years' experience in applied cybersecurity is required, alongside proven leadership in technical roles and excellent English language skills. This position offers an opportunity to contribute to innovative solutions across critical sectors. #J-18808-Ljbffr

Location: Spain (Madrid or Barcelona based) Optimapharm is a mid-sized, global Contract Research Organisation turning science into hope through agile, patient-focused clinical development. At Optimapharm, you'll have the opportunity to work on diverse and meaningful projects that help bring innovative therapies to patients worldwide. As part of our international team, you'll collaborate with experts across multiple disciplines, gain exposure to a broad range of therapeutic areas, and contribute to research that makes a real difference. With colleagues in 26 countries and operations in more than 40 countries, we combine global reach with the agility, collaboration, and supportive culture of a mid-sized organisation. Here, your expertise is valued, your growth is encouraged, and your work has a visible impact. We're searching for a CRA who is motivated by quality, driven by purpose, and eager to contribute to innovative clinical research that changes lives . At Optimapharm, your dedication is rewarded with meaningful growth opportunities, exposure to diverse studies, and the support needed to reach your full potential. • Working in a successful company that’s growing and developing every day, • Being part of a clinical research team that transforms science into hope for patients, • International projects and professional growth, • Performance bonus, • Referral bonus, • Flexible work hours, • Work from home allowance, • Additional Health Insurance, • Shopping discounts, • Employee engagement programs, • Well-being initiatives, • Training and development program, • University degree in medicine, pharmacy, dentistry, or equivalent, • At least 4 years of independent clinical trial monitoring experience (oncology, neurology, infectious diseases experience is a plus), • Strong interest in clinical research and excellent understanding of the clinical trial process, • Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements, • Fluent in local language and English, both written and verbal, • Computer proficiency is mandatory, • Ability to read, analyze, and interpret common scientific and technical journals, • Excellent verbal and written communication skills, • Excellent interpersonal and negotiation skills, • Ability to work with minimal supervision, pro-active, • Affinity to work effectively and efficiently in a matrix environment, • Excellent numerical skills and reasoning ability, • A current, valid driver’s license, • Perform routine site visits independently, including pre-study, initiation, interim monitoring and closeout visits across the region, • Manage assigned sites by regular contact with site personnel to ensure site compliance, adequate enrolment and understanding of study requirements, • Independently perform CRF review; generate and resolve queries against established data review guidelines or data management systems as applicable, • Identify and elevate potential risks and identify retraining opportunities, • Prepare corrective and preventive (CAPA) plans for issues identified during monitoring activities and pro-active follow-up on each individual CAPA until timely resolution, • Prepare documents required for EC submissions and notifications, translate study-related documents (where applicable), and perform other tasks as instructed by the supervisor, • Independently negotiate study budgets with potential investigators and institutions and assist with the execution of site contracts as applicable, • Support administration of site payments in accordance with relevant project instructions Compensation is competitive and final offers will reflect each candidate’s experience, skills, and qualifications. Disclaimer: Unsolicited CVs sent to Optimapharm (Talent Acquisition Team, Hiring Managers or any other OPT employee) by recruitment agencies will not be considered for this role. Optimapharm follows a direct sourcing strategy and collaborates exclusively with selected recruitment partners when external support is required. #J-18808-Ljbffr

LRQA Edinburgh is seeking experienced trainers to deliver face-to-face in-store training in Spain, ensuring operational teams meet global standards. Sessions blend technical procedures with soft skills to enhance customer experience and quality. Trainers conduct 150-minute in-store sessions, focusing on product prep, machine handling, service, food safety, compliance, leadership, and conflict resolution. Reports with observations and improvements follow each visit. #J-18808-Ljbffr

Optimapharm in Spain is seeking a Clinical Research Associate (CRA) to monitor sites across oncology, neurology, and infectious diseases. Based in Madrid or Barcelona, you will perform routine site visits, ensure regulatory compliance, and support data quality in active trials. You will join a global CRO focused on patient-centered development, offering international projects, a clear career path, and performance incentives. #J-18808-Ljbffr

Morningstar is a leading global provider of independent investment insights, serving both individual and institutional investors across public and private markets. Our offerings include a wide range of data, research, and investment management services, with $300+ billion in assets under management. Operating in 32 countries, Morningstar supports financial advisors, asset managers, retirement plan providers, and more with comprehensive investment solutions. Our EMEA Data Team is looking for an Associate Data Research Analyst to process our data across global markets. We are a team of data analysts who have effective relationships with other teams and are committed to deliver the best quality data. As an Associate Data Research Analyst in the Data Division, you will work closely with the global team, taking responsibility for data coverage, quality, and timeliness to the highest standards. The position will be based in our Data and Development Center EMEA in Madrid. • Work with our Data Research Analysts on the collection and maintenance of Morningstar data, ensuring high levels of data accuracy, completeness and coverage., • Assist the Data Research Analysts to meet the predetermined production deadlines., • Work as part of our project teams who evaluate procedures, create and enhance analytical tools., • Help analyzing investment data points and calculations, answering questions from other members of the data team., • Organize meetings and support the day to day activities of the Analyst team., • Utilize project management methodologies such as LEAN Six Sigma to track, evaluate and determine resolution approach for complex data issues., • Continuous communication with fund companies and 3rd party Data providers to collect data for our databases., • Fluency in Japanese and English is required, and fluency in any European language is a plus., • Solid understanding of the financial industry and passionate about investment data., • Solid analytical skills with the ability to collect, organize, analyze and disseminate large amounts of data with attention to detail and accuracy., • Previous experience in project management and knowledge of Microsoft Office are a plus. At Morningstar, every hire we make strengthens our mission to empower investor success. Apply now and help shape future of investing with us. #J-18808-Ljbffr

Amazon is seeking an ISX Partner Coach in Spain to lead in-store returns improvements across partner locations. You will field-train partner teams, analyze performance data, and drive scalable programs to elevate the customer experience. As a founding member of the EU ISX initiative, you will shape strategies, design rollout plans, and build processes while traveling frequently within Spain and across EU locations. Fluent Spanish and English required. #J-18808-Ljbffr

A leading data and investment firm located in Madrid is seeking an Associate Data Research Analyst to join their EMEA Data Team. The individual will work closely with Data Research Analysts to ensure high levels of data accuracy and meet production deadlines. Requirements include fluency in Japanese and English, strong analytical skills, and a solid understanding of the financial industry. The role offers the opportunity to apply project management methodologies and engage with various stakeholders, enhancing the quality of investment data. #J-18808-Ljbffr

We are seeking an experienced Clinical Research Associate (CRA) to support monitoring and site management activities across multiple studies. The role involves close collaboration with study teams, sites, and cross-functional stakeholders, with a strong commitment to patient safety, data integrity, and product quality. • Conduct on-site and remote monitoring activities , including visit preparation, follow-up, site contact, and report writing., • Support site start-up activities , including EC/CA submissions, contract negotiation, and essential document collection., • Attend study meetings and collaborate with cross-functional teams and sites throughout all study phases., • Provide support in audit preparation and responses ., • Schedule and conduct monitoring visits according to the study monitoring plan., • Review informed consents, regulatory files, and site study documentation , ensuring compliance with study protocols and applicable regulations (ISO 14155:2020, ICH-GCP)., • Identify and report compliance issues, working with project management to ensure timely resolution., • Ensure monitoring reports are finalized within 28 days of each site visit., • Provide interim site management services, including remote monitoring, as required., • Prior CRA experience (on-site and remote) within medical devices or pharma (ISO 14155:2020, ICH-GCP)., • Strong knowledge of EC/CA submission processes and regulatory requirements., • Excellent organizational and communication skills, with ability to collaborate across cross-functional teams., • Proactive, detail-oriented, and committed to patient safety and quality standards. ✨ This opportunity offers involvement in multiple excluively sponsor studies , exposure to a wide range of clinical operations, and the chance to work in a dynamic, high-quality environment. #J-18808-Ljbffr