Educación jobs in Sant Just DesvernCreate job alertsFull-time

General TasksUse project management software tools to manage, track, and report on projects throughout the entire project lifecycle. Create and manage key project documentation such as project charters, meeting minutes, KPIs, and project closure presentations. Job SummaryAs a Project Manager on our

Job descriptionYour mission As Global HEOR Lead, reporting to the Head of Market Access you will lead the development and execution of our global Health Economics and Outcomes Research strategy, generating robust, relevant and timely evidence to demonstrate the value of our medicines throughout

Job Description:About the RoleDow Jones Risk & Compliance is a global provider of third-party risk management and regulatory compliance solutions.Obtenga más información sobre las tareas generales relacionadas con esta oportunidad a continuación, así como sobre las habilidades requeridas.We deli

EURThe base salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically. Benefits: Read our handbook to learn about all the ways we’l

Are you being referred to one of our roles by a connection in Alira Health? If so, please apply using the referral link emailed to you.Join our global team dedicated to innovation and initiative, where physical walls and different time zones don’t limit, but encourage, collaboration.Tiene su CV pr

Clinical Research AssociateIQVIA Spain is looking for talented and motivated team member to join our Sponsor dedicated team as CRA.No espere a enviar su solicitud después de leer esta descripción; se espera un gran volumen de candidaturas para esta oportunidad.At this position you will have the op

Job Description:Job DescriptionR&C Data Research EditorAugust26Job Title: Research Editor, Risk & Compliance DataAbout the RoleDow Jones Risk & Compliance is a global provider of third-party risk management and regulatory compliance solutions.

We Are Waiting for YouHi there! I am Álvaro Gallego, the recruiter for this position.Envíe su solicitud a continuación después de leer todos los detalles y la información de apoyo sobre esta oportunidad de trabajo.Nice to meet you! First, a little bit about what I like the most about working at

IQVIA Biotech is hiring Clinical Research Associate in Spain!IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas.Si desea conocer los requisitos para este puesto, siga leyendo para obtener toda la in

You will report to the Research Manager, Business of Sports Initiative. Show flexibility to be a team player and collaborate on other projects as neededYou Have0-2 years of relevant experienceKnowledge of and interest in economics, financial markets and businessExpert-level research and investigativ

This is a hands-on senior individual-contributor role. Excellent written and spoken English and clear, credible communication with senior stakeholders.

Location & Work model: Spain | RemoteSalary & Benefits: 40,000 Desplácese hacia abajo para obtener una visión general completa de lo que requerirá este trabajo. ¿Es usted el candidato adecuado para esta oportunidad? - 55,000 gross per year (depending on experience)What's the project?Our client is a global Atlassian consulting leader on a mission to expand their reach and accelerate digital transformation within the Spanish market. With Atlassian shifting heavily toward Cloud ecosystems, enterprise organizations urgently require top-tier expert guidance to migrate, optimize, and manage their environments seamlessly.Having already transformed thousands of clients and achieved Platinum Partner status across multiple European regions, they are now bringing that same top-class expertise to boost Spanish businesses. You'll be joining a team positioned right at the heart of this regional expansion!And your role in this?As the Atlassian Consultant & Trainer, you will act as the trusted technical and strategic advisor guiding enterprise customers through complex Cloud migrations and ITSM implementations. Your main mission is to translate complex Atlassian ecosystems into clear, scalable, and operationally sound solutions while empowering customer teams through effective technical delivery and training.You will own end-to-end cloud transitions, customize Atlassian suites to align with client operations, and support pre-sales initiatives with high-impact technical expertise.More specifically, you will:Lead end-to-end cloud migration projects (Data Center Cloud), ensuring smooth transitions of data, apps, and custom workflows.Consult clients on service management, ITSM best practices, and workflow optimization across diverse business units.Configure, customize, and maintain Jira, Confluence, and broader Atlassian Cloud solutions.Support pre-sales by joining customer calls with expert input and technical direction.Deliver training and enablement sessions to help client teams adopt and master their Atlassian environments.Work across multiple clients and projects simultaneously, integrating quickly into delivery teams with strong initiative and proactivity.Ok, what should you bring?We’re looking for a skilled consultant who excels at tackling complex multi-client projects, values strategic problem-solving, and communicates technical concepts with ease.The Must-Haves:Experience: Background working in tech consulting environments managing multiple client accounts, projects, or enterprise workflows.Service & Cloud Mastery: Solid foundation in ITSM/service management principles and cloud consulting practices.Languages: High-level professional fluency in French paired with a good command of English. Clear communication skills that make complex technical topics simple are essential.Problem-Solving Agility: Hands-on ability to jump into varied client environments, assess pain points quickly, and drive continuous optimization.The Nice-to-Haves:Spanish proficiency is strongly preferred and a definite plus!Direct experience working within the Atlassian ecosystem (Jira, Confluence, Jira Service Management, etc.).Active or legacy Atlassian certifications.Team leadership experience (retrospectives, salary talks, people management).Strong background in Agile project management and delivery frameworks.Is that it?Not quite! Beyond the work itself, here is a glimpse into the vibe, package, and reality of the role:The Target & Challenge: Driving cloud transformations across traditional industries isn't always easy—you'll need to navigate cross-functional team dynamics, manage dependencies early, and bring diverse stakeholders along on the modern ITSM journey.The Salary & Package: A fixed annual salary ranging between 40,000 and 55,000 gross per year based on experience, accompanied by a remote setup and the stability of joining a recognized European market leader.The Vibes: Collaborative, growth-focused, and deeply flexible with a 100% remote working model. xiphteb You’ll be part of a forward-thinking delivery culture where continuous learning is supported and proactivity is genuinely rewarded.Discipline(s): Information TechnologiesJob type: Senior level - 3 to 5 years

IQVIA is seeking a Clinical Monitoring Analyst (Cluepoints) to work remotely across multiple geographies.The role focuses on setting up and refreshing the Centralised Monitoring platform, performing CM programming and data quality assessments, and ensuring alignment with the CMP and study protocol.T

En esta posición apoyarás la monitorización de ensayos clínicos de fases II–III para una empresa del sector farmacéutico/CRO con presencia nacional e internacional.Trabajarás en Barcelona desde un modelo híbrido, colaborando con centros hospitalarios y equipos clínicos para asegurar cumpli

In this Insurance Transformation Lead role, you guide cross-functional teams to deliver end-to-end transformations for claims, pricing, and underwriting.You will work with global, multi-disciplinary colleagues to scale insurance transformation programs across international engagements.You contribute

Dow Jones is seeking a Manager, Sports Franchise Data to lead a team of researchers responsible for building and maintaining a comprehensive database of global sports franchises.

• Design and implement the institution's strategic research plan, aligned with academic and accreditation objectives., • Identify and manage funding calls (national, European, and international) relevant to the school's research lines., • Coordinate the preparation, submission, and technical-financial justification of research projects., • Track the faculty's scientific output indicators (publications, conferences, patents, theses) and keep the institutional research database up to date., • Support faculty in preparing applications for research bonuses (sexenios), accreditations (AQU, ANECA), and research activity evaluation processes., • Manage research ethics committees and ensure regulatory compliance (intellectual property, data protection, scientific integrity)., • Establish and maintain partnerships with universities, research centers, companies, and public bodies for collaborative projects., • Prepare periodic monitoring reports and the annual research report for management and accreditation bodies., • Organize and promote scientific outreach activities (conferences, seminars, internal workshops)., • Oversee the budgetary management of research projects in coordination with the finance department., • Represent the institution before research networks and consortia in the education and creative sectors., • University degree (Master's or PhD preferred/valued) in fields related to academic management, research, business administration, or disciplines connected to LCI's teaching areas (design, fashion, art, management, technology)., • Minimum 3-5 years of experience in research management in a university or higher education setting., • Demonstrable experience managing competitive funding calls (H2020/Horizon Europe, Ministry, AGAUR, etc.)., • Knowledge of the Spanish and Catalan university system and accreditation processes (AQU Catalunya, ANECA)., • Native or advanced level (C1-C2) Spanish and Catalan., • Advanced English (C1), essential for drafting international proposals., • Proficiency with project management platforms and research databases., • Knowledge of intellectual property regulations and research ethics., • Analytical skills for reporting and KPI tracking., • Leadership and ability to work with faculty and research profiles., • Excellent communication and technical/scientific writing skills., • Results-oriented, able to manage multiple simultaneous projects., • Proactive, autonomous, with strong negotiation skills with external entities., • Commitment to academic quality and educational innovation. #J-18808-Ljbffr

Excellent program and project management skills.

Overview As a Clinical Research Associate at IQVIA in Spain, you will support sponsor-driven trials across multiple therapeutic areas. You will conduct site visits, contribute to recruitment planning, and ensure regulatory compliance and data integrity. You will work with study sites and client representatives to drive progress and quality. This role offers international exposure, growth resources, and a stable, reputable environment where your contributions advance patient outcomes. Compensaciones / Beneficios • Mobile phone, • attractive benefits package, • flexible work schedules, • resources for career growth, • programs to build therapeutic knowledge Responsabilidades, • Perform site selection, initiation, monitoring and close-out visits, • Support the development of a subject recruitment plan, • Evaluate site practices for regulatory compliance (GCP/ICH), • Manage progress by tracking regulatory submissions, recruitment, CRF completion, and data query resolutions, • Collaborate with study site experts and client representatives Requisitos principales, • University degree in scientific discipline or health care, • Experience in Pharma Industry and/or Clinical Trials, • Very good computer skills including MS Office, • Excellent command of Spanish and English, • 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, • Relationship-building and stakeholder management, • Communication and collaboration, • Adaptability and flexibility, • Problem-solving orientation, • MS Office, • GCP/ICH knowledge and compliance

En esta posición apoyarás la monitorización de ensayos clínicos de fases II–III para una empresa del sector farmacéutico/CRO con presencia nacional e internacional.Trabajarás en Barcelona desde un modelo híbrido, colaborando con centros hospitalarios y equipos clínicos para asegurar cumpli

Overview As a Junior CRA at IQVIA Spain, you will support sponsor-directed clinical studies across therapeutic areas, gaining hands-on experience in site management and regulatory processes. You will work with study sites and client teams to ensure high-quality trial execution and data integrity. This role offers growth within a stable, international company and exposure to a wide range of trials. You will contribute to advancing patient outcomes by helping manage trials efficiently and compliantly. Compensaciones / Beneficios • mobile phone, • career growth resources, • flexible work schedules, • competitive benefits package Responsabilidades, • Perform site selection, initiation, monitoring, and close-out visits, • Support development of a subject recruitment plan, • Evaluate site practices for quality and regulatory compliance (GCP/ICH), • Manage progress by tracking submissions, recruitment, CRF completion, and data query resolutions, • Collaborate with study-site experts and client representatives Requisitos principales, • University degree in scientific discipline or health care, • Experience in Pharma Industry, and/or Clinical Trials environment, • MS Office proficiency, • Excellent command of Spanish and English, • Strong organizational, time management and problem-solving skills, • Ability to establish and maintain effective working relationships, • Flexibility to travel, • Driver’s license class B, • Communication, • Teamwork, • Adaptability, • Problem-solving, • Relationship management, • MS Office

Overview In this role you will lead strategic UX research across multiple enterprise projects at Zurich's Technology Delivery Center in Barcelona. You’ll uncover user needs for internal users like underwriters and claims handlers, shaping user-centred solutions and innovative experiences, including AI-enabled interfaces. You will collaborate with cross-functional teams to turn insights into actionable recommendations and drive evidence-based decisions. This position offers hands-on research leadership in a collaborative, growth-oriented environment with a global insurance footprint. Compensaciones / Beneficios • Flexible working model, • Opportunity to work abroad up to 25 days yearly, • Home office setup allowance and monthly home office allowance, • Wide range of trainings including language courses, • Ticket restaurant and health insurance, • Life and accident insurance; retirement plan; banking and exclusive employee discounts Responsabilidades, • Lead end-to-end research across multiple projects from discovery to recommendations, • Collaborate with UX/UI designers, product owners, engineers, architects, and stakeholders, • Support product teams by identifying user needs, pain points, and opportunities, • Contribute to design and validation of experiences including conversational AI and intelligent workflows, • Drive evidence-based decisions using qualitative and quantitative insights, • Explore new research approaches, tools, and technologies to improve user understanding, • Manage multiple initiatives simultaneously while maintaining high research quality and impact, • Contribute to a culture of curiosity, collaboration, and continuous learning Requisitos principales, • Significant experience as a UX Researcher on digital products or complex user journeys, • Proficiency with diverse research methods: interviews, usability tests, discovery, surveys, workshops, validation, • Ability to translate findings into clear, actionable insights for product, business, and design decisions, • Comfort navigating ambiguity and balancing business objectives with user needs, • Experience in complex stakeholder environments and strategic thinking to link user insights to business goals, • Proactive, curious, and focused on continuously improving products and ways of working, • Strong storytelling and communication skills to influence decisions with evidence, • Experience with multiple initiatives and shifting priorities, • Desirable: experience with AI-enabled experiences, conversational interfaces, automation; strong advantage: UX/UI design, prototyping, Figma, service design, or front-end tech, • Curiosity, • Collaboration, • Communication, • UX research methodologies, • AI-enabled experiences and conversational interfaces (desirable), • Figma (desirable)

Manejo de plataformas de gestión de proyectos y bases de datos de investigación. Apoyar al profesorado en la preparación de solicitudes de sexenios, acreditaciones (AQU, ANECA) y procesos de evaluación de la actividad investigadora. Dar seguimiento a los indicadores de producción científica de

Overview As a Project Manager in Novanta’s R&D team, you will shepherd new robotic products from concept to launch. You’ll gain hands-on, cross-functional experience across hardware, software, procurement, and manufacturing, guiding projects within a growing robotics and automation portfolio. You’ll work with engineers and leaders to develop, monitor, and deliver programs on time and to quality. This role offers clear visibility, growth, and a chance to contribute to mission-critical automated solutions. Responsabilidades • Lead cross-functional teams (engineering, product management, procurement, sales, manufacturing) to meet scope and schedules, • Create and follow project management plans aligned with ISO 9001 Product Development Process and regulatory requirements, • Track RAID items (risks, issues, dependencies, assumptions) and document key decisions, • Manage resources and support project staffing, • Develop and maintain project documentation (charters, meeting minutes, KPIs, closure presentations), • Manage timelines to ensure on-time, on-scope, quality deliverables, • Interface with customers and suppliers to ensure clear communication with internal stakeholders, • Coordinate project activities with customer/product development processes and prepare business reviews for executives, • Collaborate with engineering teams to align with roadmaps and capability development, • Utilize project management tools to track, report, and communicate progress, • Lead project meetings and provide reliable updates to stakeholders, • Attend customer meetings to align requirements and capture notes, • Ensure compliance with quality, environmental, and safety regulations Requisitos principales, • Bachelor’s degree in engineering or related field, • 1-3 years of Project Management experience, • 3-5 years cumulative project experience, • Ability to collaborate across disciplines, • Self-motivated with the ability to work independently, • Proficiency in Microsoft Office, • Strong verbal and written English communication, • Familiarity with Smartsheet or MS Project (or similar) desired, • PMP certification a plus, • Familiarity with ISO9001 or ISO13485 compliance a plus, • Travel ~10% or less, • Team-oriented with good communication, • Proactive and self-driven, • Collaborative across diverse disciplines, • Microsoft Office proficiency, • Smartsheet or MS Project familiarity, • PMP (preferred)

Overview In this role you guide enterprise clients through Cloud migrations and ITSM implementations within a leading Atlassian consulting firm expanding in Spain. You translate complex Atlassian ecosystems into scalable, operational solutions and empower client teams through delivery and training. You own end-to-end cloud transitions, tailor Jira and Confluence to client needs, and support pre-sales with technical direction. You join a remote-first, growth-oriented delivery culture driving cross-client impact. Compensaciones / Beneficios • remote work, • growth-focused culture, • continuous learning opportunities Responsabilidades, • Lead end-to-end cloud migration projects (Data Center to Cloud), • Advise on ITSM best practices and workflow optimization across business units, • Configure and maintain Jira, Confluence, and Atlassian Cloud solutions, • Support pre-sales with expert input and technical guidance, • Deliver training and enablement sessions for client teams, • Collaborate across multiple clients and projects with proactive delivery Requisitos principales, • Experience in tech consulting with multiple client accounts or enterprise workflows, • Solid ITSM and cloud consulting background, • Fluent in French and proficient in English, strong communication skills, • Hands-on problem-solving ability in varied client environments, • Strong communication of complex topics, • Strategic problem-solving, • Proactivity and initiative, • Atlassian Jira, • Atlassian Confluence, • Jira Service Management

In this role you will lead and oversee clinical trial monitoring as a senior CRA within Alira Health’s global Clinical team.You will work independently and with cross-functional partners to ensure protocol compliance, quality, and timely site visits across Spain and Europe.You will shape monitorin

Overview In this role you will perform original research to gather and validate complex data for sports franchises, focusing on ownership and financing information. You will work within the WSJ Sports Intelligence team to ensure data quality and consistency in our databases, collaborating across teams and stakeholders. You will apply in-house processes, verify information through interviews, and contribute to workflow improvements with an automation mindset. The position combines rigorous research with fast-paced delivery to support data-driven sports insights. Compensaciones / Beneficios • Comprehensive Healthcare Plans, • Paid Time Off (30 days a year), • Meal Vouchers, • Retirement Plans, • Education Benefits, • Family Care Benefits & Caregiving Support Responsabilidades, • Conduct original research to input or update data from diverse sources (Internet, government records, etc.), • Master in-house processes and ensure data quality and consistency in databases, • Contact and interview company officials to verify financing and proprietary information, • Drive workflow improvements and tool efficiencies through automation-minded approaches, • Operate under tight deadlines and collaborate on additional projects as needed, • Collaborate with team members to support broader research initiatives Requisitos principales, • 0-2 years of relevant experience, • Knowledge of economics, financial markets and business, • Expert-level research and investigative skills with proficiency in advanced online search tools and proprietary databases, • Experience handling large volumes of information, • Sharp attention to detail and ability to see the bigger picture, • Openness to different views and appreciation for team diversity, • team player, • attention to detail, • initiative, • advanced online search tools, • proprietary databases, • data validation

At IQVIA, Patient & Site Centric Solutions (PSCS) brings together capabilities focused on improving the experience and outcomes of patients, sites and customers across clinical development. We are looking for an experienced Strategic Project Manager who combines strong project management expertise with a solid understanding of the clinical research and life sciences industry. In this highly visible role, you will lead and support complex AI and strategic initiatives across PSCS and our broader site businesses. You will work with stakeholders across functions and geographies, bringing structure to complex priorities and helping translate strategy into clear plans, coordinated execution and measurable outcomes. The scope will include projects across the wider PSCS organization and site busin • Define and validate project scope, objectives, deliverables, timelines and measures of success., • Support the development and management of the PSCS AI strategy and how that translates in to key projects and priorities., • Build clear project plans and governance structures to support successful execution., • Drive complex, cross-functional projects from planning through delivery, maintaining momentum, visibility and accountability., • Manage project scope, timelines, resources and costs while navigating changing business priorities., • Establish strong relationships with stakeholders across functions and business areas., • Create alignment around project objectives, responsibilities, dependencies and expected outcomes., • Coordinate multiple workstreams and stakeholders, ensuring teams remain connected and focused on agreed priorities., • Communicate progress, risks, decisions and dependencies clearly to senior stakeholders., • Proactively identify risks and potential barriers to delivery and develop effective mitigation plans., • Manage competing priorities and interdependencies across complex initiatives., • Apply structured project management methodologies and operational-effectiveness principles to business challenges., • Help teams establish practical ways of working that support successful project delivery., • Assess how strategic initiatives will affect teams, processes and ways of working., • Build awareness and support for change across the organization., • Contribute to training, communication and adoption activities where appropriate., • Evaluate project outcomes against agreed success measures., • Identify opportunities to improve or redesign processes to increase efficiency and effectiveness., • Significant project, program or PMO experience within a CRO, pharmaceutical, biotechnology, clinical research or closely related life sciences organization., • Strong understanding of the clinical research/life sciences environment and the ability to quickly understand business and operational challenges within this space., • Proven experience leading complex, cross-functional strategic projects., • Strong project planning, governance, risk management and execution capabilities., • Experience working with senior stakeholders across multiple functions and geographies., • Demonstrated ability to coordinate multiple priorities, workstreams and dependencies., • Strong stakeholder-management and influencing skills, including the ability to drive progress without direct authority., • Experience supporting organizational change, operational effectiveness or process improvement., • Strong analytical, organizational and problem-solving capabilities., • Excellent written and verbal communication skills in English., • Bachelor’s degree or an equivalent combination of relevant education and professional experience., • Будет плюсом: Experience working within a PMO, strategic transformation or operational effectiveness function; Knowledge of Lean or other continuous-improvement methodologies; Advanced project management education, training or certification; Experience delivering strategic initiatives across complex, matrixed organizations This is an opportunity to work on strategic initiatives that reach across PSCS and our broader site businesses rather than focusing on one narrow project area. The role offers exposure to a wide range of stakeholders, business challenges and strategic priorities. You’ll have the opportunity to use your clinical research industry knowledge alongside your project management expertise to help turn important business priorities into structured, measurable delivery. #J-18808-Ljbffr

Overview As Global HEOR Lead, you will shape the strategic direction and execution of our health economics and outcomes research across the product lifecycle. You will collaborate with cross-functional teams to align evidence needs with payer requirements, strengthening our value proposition and access timelines. Your work will span economic modeling, evidence synthesis, and HTA support to drive sustainable reimbursement. This role offers opportunities to influence global access, scientific excellence, and cross-border collaboration in a dynamic, patient-centric environment. Compensaciones / Beneficios • volunteering activities, • flexible working model, • collaborative office environment, • development and learning opportunities, • remuneration customization Responsabilidades, • Define and execute the global HEOR strategy across the product lifecycle within the integrated product strategy, • Lead generation of HEOR evidence including cost-effectiveness, budget impact, and other economic analyses, • Serve as HEOR technical lead for HTA submissions and support local negotiations, • Provide strategic HEOR input to value strategies and integrated evidence generation plans, • Develop and deliver HEOR training, tools, and standards to build capabilities, • Lead HEOR publication planning and foster external collaborations Requisitos principales, • Advanced degree in Health Economics, Outcomes Research, Public Health, Pharmacy, Epidemiology, Biostatistics or related scientific discipline; PhD preferred, • Extensive HEOR experience with global strategy leadership in pharma/biotech/healthcare consulting or rare disease, • Strong HTA, market access and payer evidence expertise with hands-on modeling and real-world data experience, • Proven ability to lead complex HEOR studies, support HTA submissions, and translate evidence into value propositions, • Experience in cross-functional, international, matrix organizations with stakeholder management and negotiation skills, • Strategic mindset with leadership and project management capabilities, • Empathy, • Humility, • Curiosity, • Health economic modelling, • Real-world evidence and outcomes research, • HTA submissions and payer evidence strategy

As a Project Manager in Novanta’s R&D team, you will shepherd new robotic products from concept to launch.You’ll gain hands-on, cross-functional experience across hardware, software, procurement, and manufacturing, guiding projects within a growing robotics and automation portfolio.You’ll work

Overview In this role you guide enterprise clients through Cloud migrations and ITSM implementations within a leading Atlassian consulting firm expanding in Spain. You translate complex Atlassian ecosystems into scalable, operational solutions and empower client teams through delivery and training. You own end-to-end cloud transitions, tailor Jira and Confluence to client needs, and support pre-sales with technical direction. You join a remote-first, growth-oriented delivery culture driving cross-client impact. Compensaciones / Beneficios • remote work, • growth-focused culture, • continuous learning opportunities Responsabilidades, • Lead end-to-end cloud migration projects (Data Center to Cloud), • Advise on ITSM best practices and workflow optimization across business units, • Configure and maintain Jira, Confluence, and Atlassian Cloud solutions, • Support pre-sales with expert input and technical guidance, • Deliver training and enablement sessions for client teams, • Collaborate across multiple clients and projects with proactive delivery Requisitos principales, • Experience in tech consulting with multiple client accounts or enterprise workflows, • Solid ITSM and cloud consulting background, • Fluent in French and proficient in English, strong communication skills, • Hands-on problem-solving ability in varied client environments, • Strong communication of complex topics, • Strategic problem-solving, • Proactivity and initiative, • Atlassian Jira, • Atlassian Confluence, • Jira Service Management

Job Description Summary Job Description ROC Technical Lead – Remote Operations Center (Wind Energy) Barcelona, Spain About us At GE Vernova, you are part of a global mission to electrify the world and accelerate the transition to more sustainable energy. With a legacy of engineering excellence and innovation, you help deliver reliable, affordable, and lower‑carbon power that supports communities, industries, and everyday life. Your work directly contributes to shaping the future of energy. About the role As a ROC Technical Lead, you support the safe and efficient operation of advanced offshore wind assets from a remote operations center. You play a key role across both commissioning and service phases, helping ensure turbines perform reliably throughout their lifecycle. You work closely with site teams and engineering experts to detect, analyze, and resolve technical issues, ensuring stable operations and continuous improvement. What you’ll do • Monitor turbine performance and respond to alarms or abnormal conditions, • Support commissioning and service activities through remote diagnostics and troubleshooting, • Assist field teams in resolving technical issues and restoring performance, • Escalate complex issues with clear and structured technical information, • Collaborate with engineering and support teams to resolve problems, • Analyse operational data to identify faults, trends, and improvement opportunities, • Support reporting and communication of technical findings, • Contribute to process improvement and operational optimisation, • Support grid outages when required, prioritising safety and compliance, • Work on a rotating weekday shift schedule with occasional on‑call support during weekends and public holidaysWhat you bring, • Bachelor’s or Master’s degree in Engineering, or equivalent experience in the wind energy sector, • Hands‑on experience with wind turbines or similar electromechanical systems in operational environments, • Ability to read electrical schematics and apply them in troubleshooting and field support situations, • Experience with SCADA systems and other digital monitoring tools, • Strong analytical and problem‑solving skills with clear technical communication, calm structured approach under pressure, and a collaborative, proactive mindset, • Availability to travel up to 20% of the time, if required., • Fluent English (spoken and written), willingness to relocate to Barcelona and EU work eligibility.Nice to have, • Control room or remote operations experience, • Offshore wind or commissioning experience, • Exposure to advanced turbine control systems (e.g., MarkVIe or similar), • Experience working in multicultural teams, • Fluent in Spanish (spoken and written)Ways of working you work on a rotating weekday shift schedule (Monday to Friday), covering morning and afternoon shifts. You also take part in an on‑call rotation for occasional weekend and public holiday support. Our culture At GE Vernova, you help drive the transition to a more sustainable energy future. Every contribution matters as we work to deliver reliable power worldwide. We support your growth through learning, development, and internal mobility, helping you build a career that evolves with you. We are committed to inclusion and diversity, creating an environment where everyone can thrive and contribute. Join us If you want to work at the forefront of wind energy and help shape the future of global power systems, this is your opportunity to make an impact. Additional Information Relocation Assistance Provided: No GE Vernova is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law. … #J-18808-Ljbffr

Own the full product lifecycle for a key platform area, from discovery and definition through delivery and continuous improvement Define and evolve product strategy and roadmaps in alignment with business goals, customers, data, and internal stakeholders Partner with engineering, design, and busines

Modelos de Lenguaje (LLMs): experiencia técnica directa implementando y consumiendo APIs de Claude (Anthropic) o similares y herramientas de código como Codex (no solo a nivel teórico, pero en entornos de producción). Infraestructura como código (IaC) y operaciones: dominio de Ansible para la g

Overview In this senior, hands-on role, you own the research agenda for Experience & Adoption within DD&IT, turning ambiguous business challenges into actionable evidence that informs product and business decisions. You collaborate with product, design, engineering, and business stakeholders to ensure research leads to meaningful action. You apply both qualitative and quantitative methods to shape decisions, while upholding ethical and inclusive research practices. You will mentor colleagues and explore AI-enabled efficiencies to strengthen research outcomes. Compensaciones / Beneficios • insurance plans, • retirement plans, • wellbeing resources, • global recognition programs, • flexible and hybrid working options, • paid parental leave Responsabilidades, • Own the research agenda aligned with business priorities and evidence gaps, • Design and execute end-to-end mixed-methods studies with appropriate sampling, • Synthesize findings into actionable recommendations with confidence and limitations, • Represent user needs in roadmap and design discussions and challenge assumptions, • Mentor colleagues, improve methods, and contribute reusable evidence to the insights repository, • Identify and apply AI to improve research workflow efficiency without compromising quality, • Ensure ethical, inclusive research with proper consent, data handling and documentation throughout the lifecycle Requisitos principales, • 8+ years of applied research experience in product or design research, • Expertise in both qualitative and quantitative methods, • Ability to frame ambiguous problems and select proportionate approaches, • Track record of research influencing meaningful product or business decisions, • Hands-on experience with enterprise-scale research tools and repositories, • Excellent written and spoken English with ability to communicate with senior stakeholders, • Accessibility and inclusive research expertise a plus, • Bachelor in Human-Computer Interaction, Cognitive Science, Psychology, Statistics, Anthropology, Design Research or related discipline, • Working knowledge of research ethics, consent, privacy and confidentiality, • strong collaboration and cross-functional influence, • clear, credible communication with senior stakeholders, • mentorship and knowledge sharing, • qualitative methods, • quantitative methods, • mixed-methods research design

En esta posición apoyarás la monitorización de ensayos clínicos de fases II–III para una empresa del sector farmacéutico/CRO con presencia nacional e internacional.Trabajarás en Barcelona desde un modelo híbrido, colaborando con centros hospitalarios y equipos clínicos para asegurar cumpli

Clinical Research AssociateIQVIA Spain is looking for talented and motivated team member to join our Sponsor dedicated team as CRA. No espere a enviar su solicitud después de leer esta descripción; se espera un gran volumen de candidaturas para esta oportunidad. At this position you will 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, and build a meaningful, strong career within our organization.Your responsibilities will include:Performing site selection, initiation, monitoring and close-out visitsSupporting the development of a subject recruitment planEvaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelinesManaging progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutionsCollaborating with experts at study sites and with client representativesQualifications:University degree in scientific discipline or health careExperience in Pharma Industry, and/or Clinical Trials environmentVery good computer skills including MS OfficeExcellent command of Spanish and English languageOrganizational, time management and problem-solving skillsAbility to establish and maintain effective working relationships with coworkers, managers, and clientsFlexibility to travelDriver’s license class BWhat you can expect: Resources that promote your career growthLeaders that support flexible work schedulesPrograms to help you build your therapeutic knowledgeExcellent working environment in a stabile, international, reputable companyMobile phone and attractive benefits packageIQVIA 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. xiphteb 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.SummaryLocation: Madrid, Spain; Barcelona, SpainType: Full time

The Barcelona Supercomputing Center - Centro Nacional de Supercomputación (BSC-CNS) is the leading supercomputing center in Spain. It houses MareNostrum, one of the most powerful supercomputers in Europe, was a founding and hosting member of the former European HPC infrastructure PRACE (Partnership for Advanced Computing in Europe), and is now hosting entity for EuroHPC JU, the Joint Undertaking that leads large-scale investments and HPC provision in Europe. The mission of BSC is to research, develop and manage information technologies in order to facilitate scientific progress. BSC combines HPC service provision and R&D into both computer and computational science (life, earth and engineering sciences) under one roof, and currently has over 1000 staff from 60 countries. We are particularly interested for this role in the strengths and lived experiences of women and underrepresented groups to help us avoid perpetuating biases and oversights in science and IT research. In instances of equal merit, the incorporation of the under-represented sex will be favoured. We promote Equity, Diversity and Inclusion, fostering an environment where each and every one of us is appreciated for who we are, regardless of our differences. If you consider that you do not meet all the requirements, we encourage you to continue applying for the job offer. We value diversity of experiences and skills, and you could bring unique perspectives to our team. We are looking for research data managers, data stewards, or equivalent professional figures, with a proven technical background, and experience in data services deployment, for contributing to BSC data and information services design and deployment, and for giving support to BSC multidisciplinary researchers. • Contribute to build up and maintain the BSC scientific data catalogues and data services and its governance tool., • Design and implement automatic procedures for adequate data validity, share, protection and security, according to the BSC mission. Ensure data and information at BSC meets standards and interoperability with respect to formats, security, confidentiality and personal data protection., • Contribute to adopt FAIR Data principles across existing and future projects that the data management team is participating at., • Collaborate with other data management groups at European and International level on practical matters related to research production, research data management and data governance., • Support and advise researchers about the BSC technical services for data and metadata management., • Train BSC personnel and users on Data Management topics., • Education, • Degree/Master’s degree in any data related scientific/humanistic discipline will be considered., • Degree/Master’s degree in software engineering will be considered in combination with a scientific specialization/background, • Specialization, or participation to courses and workshops on data management related topics will be positively considered, • PhD or research experience with a strong technical data management component will be positively considered., • Essential Knowledge and Professional Experience, • Experience with designing and developing tools for data management, especially for data management planning and data publication., • Experience with automatizing processes for data management., • Strong knowledge and proven professional experience on databases., • A thorough understanding of managing data and on Open Science principles, • A thorough knowledge of the FAIR data principles and their practical application., • Additional Knowledge and Professional Experience, • Experience working in a scientific research environment., • Experience on giving training on data management topics, • Good understanding of Linux environment and Shell scripting., • Experience working in a public center, with basic knowledge of the legal framework for treating with personal and confidential data., • Fluency written and verbal communication skills in English., • Good written and verbal communication skills in Spanish., • Competences, • Ability to take initiative, prioritize and work under set deadlines., • Ability to work independently and in a team., • Excellent communication and collaboration skills with technical and non technical staff., • The position will be located at BSC within the AI Institute, • We offer a full-time contract (35h/week), a good working environment, a highly stimulating environment with state-of-the-art infrastructure, flexible working hours, extensive training plan, restaurant tickets, private health insurance, support to the relocation procedures, • Duration: Temporary - 27 months, • Holidays: 22 days of holidays + 6 personal days + 24th and 31st of December per our collective agreement, • Salary: we offer a competitive salary commensurate with the qualifications and experience of the candidate and according to the cost of living in Barcelona, • Starting date: asap The vacancy will remain open until a suitable candidate has been hired. Applications will be regularly reviewed and potential candidates will be contacted. BSC-CNS is committed to the principles of the Code of Conduct for the Recruitment of Researchers of the European Commission and the Open, Transparent and Merit-based Recruitment principles (OTM-R). This is applied for any potential candidate in all our processes, for example by creating gender-balanced recruitment panels and recognizing career breaks etc. BSC-CNS is an equal opportunity employer committed to diversity and inclusion. We are pleased to consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or any other basis protected by applicable state or local law. For more information follow this link. Please contact For more information, please follow this link. #J-18808-Ljbffr

Webfleet seeks an experienced Trainer to join our Corporate Training Team. You will design and deliver training across Inside and Field Sales, across regions, with a focus on consultative selling and leadership development. You will own onboarding, build soft skills programs, and partner with Sales Enablement, Quality, Customer Success, and HR to ensure learning is aligned with business priorities and measurable outcomes. This role requires global delivery and a dynamic, collaborative mindset. #J-18808-Ljbffr

SumUp in Barcelona is seeking an experienced Sales Enablement professional to own onboarding and skills development for telesales and account management across multiple European markets. You design and deliver live training, run onboarding sessions, and track impact through assessments and shadowing. You will collaborate with team leads and EU leadership to build programs that raise sales volume and cross-sell. #J-18808-Ljbffr

LCI Education in Barcelona seeks a Research Management Lead to design and implement the institution's strategic research plan in line with accreditation objectives. You will identify funding calls, coordinate proposals, monitor outputs, and manage ethics and IP compliance, partnering with universities and industry to advance innovative projects. Fluency in Spanish and Catalan, strong writing and negotiation skills, and a track record in higher education research administration are required. #J-18808-Ljbffr

Overview In this role you will lead and oversee clinical trial monitoring as a senior CRA within Alira Health’s global Clinical team. You will work independently and with cross-functional partners to ensure protocol compliance, quality, and timely site visits across Spain and Europe. You will shape monitoring plans, mentor junior CRAs, and collaborate with sponsors to resolve site issues, driving project success and study timelines. This position offers exposure to international teams and a mission-driven, inclusive culture. Compensaciones / Beneficios • remote work, • international team, • competitive salary range 55k-70k, • full-time contract, • location flexibility (Barcelona-Remote; Europe-Remote), • professional development opportunities Responsabilidades, • Provide guidance and oversight to the CRA team to meet scope, SOPs, timelines, and budgets, • Review monitoring visit reports and conduct co-monitoring and evaluation visits as needed, • Coordinate with cross-functional departments to resolve monitoring-related issues, • Assist in development of monitoring plans and training materials, • Assist in ethics documents setup and site contract negotiation, • Provide monthly billing information to finance, • Manage study budget for monitoring stand-alone projects and act as sponsor referent, • Perform qualification, initiation, interim, and close-out visits both remotely and onsite, • Document monitoring visits with clear reports on problems, resolutions, and enrollment status, • Ensure data integrity through source document review and eTMF/TMF verification, • Conduct investigational product accountability and review regulatory binders, • Maintain site communication to ensure GCP compliance and address sponsor requests, • Comply with ICH GCP, FDA regulations, and SOPs; participate in required meetings, • Facilitate adverse event reporting and reconcile SAE with sources and CRFs, • Collaborate with CRAs, data management to resolve data discrepancies, • Identify site issues and develop problem-solving strategies, • Support CRA onboarding and mentoring; contribute to CTMS maintenance, • Manage conflicting priorities to deliver on commitments, • Perform additional duties as assigned Requisitos principales, • BS/BA in life sciences or related discipline (US), • 3 years in pharma/biotech/CRO with 2 years clinical monitoring and 1 year management experience (US), • EU: at least 2 years of clinical monitoring experience with capability to autonomously manage monitoring activities, • Strong knowledge of ICH GCP and regulatory requirements, • Excellent communication and interpersonal skills; customer service orientation, • Ability to travel and manage stress; professional and trustworthy, • English proficiency (US) or Local language proficiency (EU), • Graduation in a scientific health field (EU), • Adequate English (EU), • quality-focused, • highly organized and multi-tasking, • problem-solving and negotiation, • CTMS knowledge, • eTMF/TMF documentation and verification, • clinical trial databases and electronic data capture

The Barcelona Supercomputing Center - Centro Nacional de Supercomputación (BSC-CNS) invites applications for a Research Engineer in System Validation within the Earth Sciences department. The role focuses on testing, validation, and optimization of climate models and associated software in national HPC environments. You will collaborate with scientists to ensure robust system performance, develop testing tools, and document validation results to support climate research and operational readiness #J-18808-Ljbffr

Overview In this full-time, home-based CRA role in Barcelona, you support patients and sites as Medpace accelerates the development of pharmaceuticals and medical devices. You join a training-focused program (PACE) to build independent CRA expertise through hands-on practice and rotations. The role offers diverse therapeutic exposure, cross-functional collaboration, and clear growth paths within a global CRO. You will contribute to compliant, high-quality study conduct with potential for mentoring and leadership opportunities. Compensaciones / Beneficios • Flexible work environment, • Competitive compensation and benefits package, • Competitive PTO, • Structured career paths with growth, • Company-sponsored employee appreciation events, • Employee health and wellness initiatives Responsabilidades, • Conduct qualification, initiation, monitoring, and closeout visits per protocol, • Communicate with site staff including coordinators and investigators, • Verify investigator qualifications, training, resources, and facilities, • Verify data accuracy and ensure Good Documentation Practices; address protocol deviations per SOPs, GCP, and regulatory requirements, • Ensure enrollment of eligible subjects and perform regulatory document reviews, • Oversee medical device/investigational product/drug accountability, • Review adverse events and concomitant medications for accurate reporting, • Assess site recruitment/retention and suggest improvements, • Complete monitoring reports and follow-up letters with actionable recommendations to ensure compliance Requisitos principales, • University degree in a health or life science related field, • Minimum 1 year experience as Study Coordinator (SC), CRC, or CRA trainee, • Approximately 60-80% travel, • Proficient Microsoft Office and general computer literacy, • Outstanding communication and presentation skills, • Detail-oriented with good time management, • Excellent verbal and written communication in English and Spanish, • Catalan language fluency is a plus, • strong communication, • attention to detail, • time management, • Microsoft Office, • Good Documentation Practices (GDP), • GCP compliance

Overview As Global HEOR Lead, you will shape the strategic direction and execution of our health economics and outcomes research across the product lifecycle. You will collaborate with cross-functional teams to align evidence needs with payer requirements, strengthening our value proposition and access timelines. Your work will span economic modeling, evidence synthesis, and HTA support to drive sustainable reimbursement. This role offers opportunities to influence global access, scientific excellence, and cross-border collaboration in a dynamic, patient-centric environment. Compensaciones / Beneficios • volunteering activities, • flexible working model, • collaborative office environment, • development and learning opportunities, • remuneration customization Responsabilidades, • Define and execute the global HEOR strategy across the product lifecycle within the integrated product strategy, • Lead generation of HEOR evidence including cost-effectiveness, budget impact, and other economic analyses, • Serve as HEOR technical lead for HTA submissions and support local negotiations, • Provide strategic HEOR input to value strategies and integrated evidence generation plans, • Develop and deliver HEOR training, tools, and standards to build capabilities, • Lead HEOR publication planning and foster external collaborations Requisitos principales, • Advanced degree in Health Economics, Outcomes Research, Public Health, Pharmacy, Epidemiology, Biostatistics or related scientific discipline; PhD preferred, • Extensive HEOR experience with global strategy leadership in pharma/biotech/healthcare consulting or rare disease, • Strong HTA, market access and payer evidence expertise with hands-on modeling and real-world data experience, • Proven ability to lead complex HEOR studies, support HTA submissions, and translate evidence into value propositions, • Experience in cross-functional, international, matrix organizations with stakeholder management and negotiation skills, • Strategic mindset with leadership and project management capabilities, • Empathy, • Humility, • Curiosity, • Health economic modelling, • Real-world evidence and outcomes research, • HTA submissions and payer evidence strategy

Una organización educativa en Barcelona está buscando un/a Project Manager para liderar proyectos estratégicos en análisis y generación de conocimiento. Esta posición implica trabajar con universidades y expertos del sector, gestionando desde la planificación hasta la publicación de resultados. Se requiere una titulación superior, con experiencia de más de 3 años en gestión de proyectos de investigación y un sólido conocimiento del sistema universitario español. Se valorarán habilidades analíticas y de comunicación. #J-18808-Ljbffr

Constructor Labs is the applied research and innovation centre of Constructor Group. We are seeking a Marketing Manager to lead positioning, messaging and demand generation for university and enterprise clients. You will own the messaging, plan, budget and results, and work hands-on while coordinating a shared marketing team. The role requires translating complex research and education services into compelling value propositions, building campaigns across channels, and collaborating with #J-18808-Ljbffr

Build a career powered by innovations that matter! At Novanta, our innovations power technology products that are transforming healthcare and advanced manufacturing—improving productivity, enhancing people’s lives and redefining what’s possible. Compruebe que cumple con los requisitos de habilidades para este puesto, así como con la experiencia asociada, y luego envíe su CV a continuación. We create for our global customers engineered components and sub-systems that deliver extreme precision and performance for a range of mission-critical applications—from minimally invasive surgery to robotics to 3D metal printing.Novanta is one global team with over 26 offices located in The Americas, Europe and Asia-Pacific. Looking for a great place to work? You have found it with a culture that embraces teamwork, collaboration and empowerment. Come explore Novanta.Company Overview Are You Ready to Take Your Next Career Step? At Novanta, we foster a culture of career development. Come explore a world of opportunities throughout our global teams. Novanta is the world’s leading developer of robotic end of arm technologies. Novanta end-effectors enhance productivity and flexibility of robotic and automated solutions across a wide spectrum of industries through capabilities such as automatic tool changing, force-torque sensing, material removal, and more. Since 1989, our commitment to engineering excellence, superior quality, and customer-focused support drives us to innovate and continuously improve the most reliable automated solutions available.Job SummaryAs a Project Manager on our Research & Development team, you’ll play a key role in bringing new products to life • from initial concept through launch. This is a great opportunity to build a strong foundation in program management while gaining hands-on, cross-functional experience working with engineers (hardware and software), product managers, procurement, sales, manufacturing, and senior leadership. You’ll help manage projects that support Novanta’s growing robotics and automation portfolio, working alongside experienced engineers and program leaders who will help develop your skills as you grow into program management. This is an individual contributor role with high visibility and strong potential for career growth within Novanta.Primary ResponsibilitiesLead and coordinate cross-functional teams • including engineering, product management, procurement, sales, and manufacturing, • to deliver projects to agreed scope and timeline. Create and follow project management plans from project inception to closure, in alignment with Novanta’s ISO 9001-compliant Product Development Process and applicable regulatory requirements. Record, track, and monitor project and program RAID items such as risks, issues, dependencies, and assumptions. Track and monitor action items through to closure and document key decisions. Manage and support project resources, including internal teams and technical resources. Create and manage key project documentation such as project charters, meeting minutes, KPIs, and project closure presentations. Manage timelines to ensure key deliverables are completed on time, within scope, and to quality standards. Interface with customers and suppliers as needed during design and development, facilitating clear communication with internal stakeholders. Support the planning and execution of projects in line with Novanta’s Product Development Process (or the customer’s development process, as applicable). Coordinate and help prepare project business reviews for senior executives, aligning with internal stakeholders such as product marketing, development, procurement, and finance. Partner with engineering teams to gain exposure to product roadmaps and capability development. General TasksUse project management software tools to manage, track, and report on projects throughout the entire project lifecycle. Host and lead project meetings to track pertinent decisions, actions, and task completion. Provide periodic, reliable updates to all internal stakeholders. Attend customer meetings as needed to align to their requirements. Capture meeting notes and minutes to facilitate project alignment as needed. Maintain strict compliance with quality, environmental, and occupational health and safety regulations, and follow the instructions of the quality, environmental management, and/or occupational health and safety officer. Required Experience, Education, Skills and Competencies Bachelor’s degree in engineering or related field 1-3 years of Project Management experience 3-5 years cumulative experience working on or managing projects Ability to work in a team environment and foster collaboration across different disciplines Motivated • be able to take direction and work independently to achieve goals Proficiency in Microsoft Office Good verbal and written communication skills in English Familiarity with Smartsheet or MS Project (or similar project management software tool experience) desired PMP certification is a plus Familiarity with ISO9001 or ISO13485 compliance is a plus Travel Requirements~10% Travel (or less) as neededNovanta is proud to be an equal employment opportunity and affirmative action workplace. We consider all qualified applicants without regard to race, color, religion, sex (including pregnancy), sexual orientation, gender identity or expression, national origin, military and veteran status, disability, genetics, or any other category protected by federal law or Novanta policy. xhfqzwm Please call if you need a disability accommodation for any part of the employment process.SummaryLocation: Barcelona, SpainType: Full time