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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

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

Job TitleManager User Experience (UX) Research & DesignBusiness EnvironmentThe Manager, UX Research & Design guides and develops a multi-disciplinary team delivering high-quality user experiences across Amadeus Hospitality products.

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

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

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 SummaryAs a Project Manager on our Research & Development team, you’ll play a key role in bringing new products to life. 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 softw

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.

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

Si sus habilidades, experiencia y cualificaciones coinciden con las de esta descripción del puesto, no demore su solicitud.Hybrid)As you contemplate your future, you might be asking yourself, " What's the next step?’’ Start your journey with us!We're seeking an experienced Senior UX Researcher

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

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

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

Clinical Research AssociateIQVIA Spain is looking for talented and motivated team member to join our Sponsor dedicated team as CRA.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

Cronoshare es una plataforma online para profesionales que quieren encontrar nuevos clientes. Buscamos Profesor/a de natación en Viladecans y alrededores. Pertenecer a la red de profesionales de Cronoshare no tiene coste y recibirás nuevos clientes según tus preferencias, de forma personalizada. Requisitos: • Conocimientos previos para desarrollar funciones de Profesor/a de natación., • Organización, buena relación con el cliente y gestión de tiempo., • Profesionalidad y proactividad. Qué ofrecemos: • Solicitudes de nuevos trabajos y clientes en tu zona, que necesitan Profesor/a de natación., • Gestión propia de los clientes y márgenes comerciales., • Sin intermediarios: tú fijas tus tarifas y horarios. ¿Cómo funciona Cronoshare? Gracias a nuestra plataforma de gestión de clientes, podrás aceptar o descartar solicitudes de trabajos en tu área, enviando presupuestos solo a los clientes que más te interesen. No pagarás suscripciones ni tarifas mensuales, además tampoco tienes que abonar comisiones por cada cliente que consigas gracias a nosotros. Para conseguir nuevos clientes, solo tienes que incurrir en una pequeña inversión y podrás acceder a estas solicitudes. Empieza a hacer crecer tu actividad comercial o negocio. Si eres freelance, autónomo o pyme, te esperamos.

Cronoshare es una plataforma online para profesionales que quieren encontrar nuevos clientes. Buscamos Profesor/a de inglés nativo en Barcelona y alrededores. Pertenecer a la red de profesionales de Cronoshare no tiene coste y recibirás nuevos clientes según tus preferencias, de forma personalizada. Requisitos: • Conocimientos previos para desarrollar funciones de Profesor/a de inglés nativo., • Organización, buena relación con el cliente y gestión de tiempo., • Profesionalidad y proactividad. Qué ofrecemos: • Solicitudes de nuevos trabajos y clientes en tu zona, que necesitan Profesor/a de inglés nativo., • Gestión propia de los clientes y márgenes comerciales., • Sin intermediarios: tú fijas tus tarifas y horarios. ¿Cómo funciona Cronoshare? Gracias a nuestra plataforma de gestión de clientes, podrás aceptar o descartar solicitudes de trabajos en tu área, enviando presupuestos solo a los clientes que más te interesen. No pagarás suscripciones ni tarifas mensuales, además tampoco tienes que abonar comisiones por cada cliente que consigas gracias a nosotros. Para conseguir nuevos clientes, solo tienes que incurrir en una pequeña inversión y podrás acceder a estas solicitudes. Empieza a hacer crecer tu actividad comercial o negocio. Si eres freelance, autónomo o pyme, te esperamos.

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

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 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

Pompeu Fabra University (UPF) Barcelona invites applications for tenure-track Assistant Professor positions in management, especially in marketing, strategy, entrepreneurship, and innovation.Appointments start in September 2027.Candidates must hold a PhD, or expect to complete one by summer 2027.The

Job Description Plan lessons in advance and send plans via email to the Head of Level and Academic Coordinator. Prepare and organize the necessary materials for classes. Fulfill the objectives outlined in the general plans distributed at the beginning of the year. Maintain the grade book up to date. Enter grades at the end of each evaluation period and semester, on or before deadlines. Design and prepare monthly assessments for each topic. Grade all assigned work. Keep the classroom decorated with materials related to lessons, activities, and holidays. Perform assigned playground supervision duties. Collaborate with the Psychology Department to support students with academic or behavioral issues. Work with the Academic Coordinator and psychologist to support students with special needs, including gifted learners. Attend meetings with teachers, academic coordinators, and assistant principals. Attend institutional workshops. Participate in parent meetings and special school activities. Comply with the established work schedule (departure time varies by grade level). Act as a mediator between students and inform the psychologist of conflicts and/or refer students experiencing emotional, personal, or family issues. Collaborate with the psychologist to organize community service projects and fundraising activities. Assist and/or organize student participation in fairs and other activities. Contact parents/guardians to invite them to meetings or special events when necessary. Record daily attendance in the system or submit forms to the Academic Support Department. Collect subject‑specific assignments for portfolio organization according to level criteria, each evaluation period. Assign a student to record homework and monitor the Homework Board, ensuring its proper use every two weeks. Encourage student participation in subcommittees to promote teamwork and school activities. Promote open communication with students and parents. Encourage parents/guardians to attend meetings organized by ISP CBNH and PTA. Consider students’ special learning and socio-emotional needs and refer them to the Psychology Department. Attend school in proper uniform and/or according to institutional policies. Perform other duties related to the position. • Field/Specialization: Bachelor’s degree in Education, Psychology, or related fields., • Master’s Degree: Preferred, • Proficiency in digital tools, • Intermediate-level Microsoft Office skills Organization (Level 4) Planning (Level 4) Leadership (Level 3) Analytical Skills (Level 4) Ability to Work Under Pressure (Level 4) Communication (Level 4) Strategic Thinking (Level 4) English Level: Advanced (must be fluent in speaking, reading, and writing) • Required, • Minimum 2 years in education ISP Principles Begin with our children and students. Our children and students are at the heart of what we do. Simply, their success is our success. Wellbeing and safety are both essential for learners and learning. Therefore, we are consistent in identifying potential safeguarding and Health & Safety issues and acting and following up on all concerns appropriately. Treat everyone with care and respect. We look after one another, embrace similarities and differences and promote the well-being of self and others. Operate effectively. We focus relentlessly on the things that are most important and will make the most difference. We apply school policies and procedures and embody the shared ideas of our community. Are financially responsible. We make financial choices carefully based on the needs of the children, students and our schools. Learn continuously. Getting better is what drives us. We positively engage with personal and professional development and school improvement. ISP Commitment to Safeguarding Principles ISP is committed to safeguarding and promoting the welfare of children and young people and expects all staff and volunteers to share this commitment. All post holders are subject to appropriate vetting procedures, including an online due diligence search, references and satisfactory Criminal Background Checks or equivalent covering the previous 10 years’ employment history. ISP Commitment to Diversity, Equity, Inclusion, and Belonging ISP is committed to strengthening our inclusive culture by identifying, hiring, developing, and retaining high-performing teammates regardless of gender, ethnicity, sexual orientation and gender expression, age, disability status, neurodivergence, socio‑economic background or other demographic characteristics. Candidates who share our vision and principles and are interested in contributing to the success of ISP through this role are strongly encouraged to apply. #J-18808-Ljbffr

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

Overview In this role, you will contribute to strategy, transformation, go-to-market, organization, and M&A work in the Healthcare sector. You will collaborate with leading Healthcare players in Spain to deliver strategy, transformation, and AI initiatives. You join a top Health Care Strategy Consulting team in Spain, with avenues for career growth and participation in national and international projects. You will work in a global, collaborative environment that combines business insight with digital capabilities to drive meaningful outcomes for clients. Responsabilidades • Contribute to strategy, transformation, go-to-market, organization and M&A projects in Healthcare, • Deliver strategy, transformation and AI projects for Healthcare clients in Spain, • Participate in a leading Health Care Strategy Consulting team in Spain with opportunities for career development and cross-border projects Requisitos principales, • At least 8 years of full-time professional experience with a Healthcare/Life Sciences/MedTech focus, • Previous consulting experience, preferably in strategy consulting with Healthcare/Life Sciences focus, • Bachelor's degree; Master's/MBA is a plus, • Local market experience preferred, • Fluency in English and Spanish, • AI projects in Healthcare, • Strategy consulting, • Healthcare industry knowledge

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

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

In this role, you lead cross-functional teams to solve high-stakes client challenges and shape data-driven strategies.You’ll synthesize insights, leverage advanced frameworks, and guide end-to-end delivery to create impactful solutions.You’ll engage senior clients, articulate compelling narrativ

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 leadership role, you will advance process effectiveness and first-line monitoring across International Medical Affairs to strengthen governance and proactive risk management. You’ll shape monitoring frameworks, translate insights into actions, and drive sustainable operational excellence with cross-functional and cross-border impact. You will champion audit readiness, data-driven improvements, and responsible use of AI and digital tools to boost efficiency and consistency. This position offers high visibility to influence how Medical Affairs teams deliver priorities while upholding compliance and quality across geographies. You’ll join a culture that values transformation, governance Compensaciones / Beneficios • insurance plans, • retirement plans, • wellbeing resources, • global recognition programs, • flexible and hybrid working options, • minimum 14 weeks paid parental leave Responsabilidades, • Lead process effectiveness and first-line monitoring to ensure consistent, compliant execution, • Design and evolve monitoring frameworks to identify governance risks, trends, and improvement opportunities, • Translate monitoring insights into corrective and preventive actions, • Drive proactive risk management and address emerging governance and compliance risks, • Strengthen audit and inspection readiness with embedded processes and accountability, • Collaborate with country, regional, and functional stakeholders to improve adoption and operational effectiveness, • Lead process simplification and transformation initiatives while upholding governance standards, • Establish metrics to assess process effectiveness and prioritize improvements, • Champion the use of AI, analytics, and digital solutions to enhance monitoring and efficiency, • Lead and develop the Process Effectiveness and Monitoring team across geographies Requisitos principales, • Advanced degree in Medicine, Pharmacy, Life Sciences, or a related field, • Minimum 10 years of Medical Affairs, Quality and Compliance experience in the pharmaceutical industry, • Experience in international, regional, or above-country Medical Affairs roles within a complex global organization, • Experience leading multi-country first-line assurance including risk-based monitoring, quality oversight, internal controls, and CAPA management, • Experience translating enterprise standards into country practice, including audit and inspection readiness and cross-country remediation, • Experience defining performance and quality indicators and translating monitoring insights for senior leadership, • Previous people leadership experience with ability to develop and empower high-performing teams across geographies, • Excellent written and spoken English with strong communication, influencing, analytical, organizational, and stakeholder-management skills, • Influencing, • Stakeholder-management, • Analytical thinking, • Monitoring frameworks, • Risk management, • Quality and compliance

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)

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 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

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

IQVIA recruits a Clinical Monitoring Analyst (Cluepoints) for a sponsor-dedicated project, with remote work options. The role centers on setting up, programming, and refreshing the Centralized Monitoring platform using SAS and Cluepoints, aligned with the study CMP to ensure quality and timely deliveries. You will interpret study protocols, manage data sources, and contribute to CM documentation while working autonomously and collaborating with global teams to protect data confidentiality and #J-18808-Ljbffr

Overview You will support clinical development as a site-focused CRA across multiple therapeutic areas from home-based Spain. You’ll drive site monitoring, ensure GCP/ICH compliance, and manage data quality while coordinating with cross-functional teams. The role blends investigator relations, regulatory tracking, and TMF/ISF maintenance to sustain study integrity. This position offers exposure to oncology, hematology, and cardiovascular trials within a collaborative, agile culture. You will contribute to delivering reliable data to accelerate patient access to innovative treatments. Responsabilidades • Perform a range of site monitoring visits (selection, initiation, monitoring, close-out) per scope and regulations (GCP/ICH), • Collaborate with sites to recruit subjects, tracking the recruitment plan to improve predictability, • Provide protocol training and maintain regular communication with sites to manage study expectations and issues, • Assess site practices for protocol compliance and data integrity; escalate quality issues as needed, • Track regulatory submissions, approvals, recruitment, CRF completion, data queries, and study progress, • Ensure TMF/ISF documents are available and maintained per GCP and local requirements, • Document site management activities, site visit findings, and action plans with reports and follow-up letters, • Collaborate with study team members to support project execution, • May support site-specific recruitment planning and, where applicable, site financial management per contract Requisitos principales, • Bachelor on scientific discipline or health care preferred, • At least 1.5 years of on-site monitoring experience, • Equivalent combination of education, training and experience considered, • Strong organizational, time management and problem-solving skills, • Ability to establish effective working relationships with colleagues, managers, and clients, • Flexibility to travel and valid driver’s license, • strong communicator, • collaborative, • adaptable, • GCP/ICH knowledge, • site monitoring and management, • TMF/ISF maintenance

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 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

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

The Department of Economics and Business at UPF provides a vibrant research environment, reflected in its strong.

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

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 a multidisciplinary UX team to deliver high-quality experiences across Amadeus Hospitality products. You’ll shape UX strategy, align research and design practices, and drive UX maturity while partnering with Product, Engineering and business stakeholders. You will support team performance, growth, and long-term capability development to meet user and business needs. The opportunity centers on influencing product direction through research insights and scalable design systems, with a strong focus on collaboration and impact. Responsabilidades • Provide strategic direction and quality oversight for design outcomes, • Ensure alignment with UX principles, accessibility standards, and design system, • Influence product scope and prioritization using research insights and design frameworks, • Promote early UX involvement across the product lifecycle, • Plan resource needs aligned with roadmaps and domain priorities, • Collaborate with Product, Engineering, leadership, and customers to shape product direction, • Define and align on research strategy; ensure insights are actionable and credible, • Increase visibility of UX research across product teams and leadership, • Encourage learning, development, and career paths within the team, • Provide coaching, mentoring, and regular feedback to designers and researchers, • Support development of competencies in research, design, communication, strategy, and cross-functional collaboration, • Delegate and empower team members to own initiatives Requisitos principales, • Experience guiding UX teams in complex SaaS environments (B2B/B2C), • Experience designing for multi-platform ecosystems (web, mobile, CRM platforms), • Experience collaborating with product, engineering, and business partners to influence strategy and roadmaps, • Strong design and research background with ability to influence product direction, • Clear and effective communication, • Facilitation and storytelling, • Collaboration across geographies and disciplines, • Advanced interaction and systems design, • Proficiency with Figma or equivalent tools, • Information architecture, prototyping, usability testing

• 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

Overview In this leadership role, you will advance process effectiveness and first-line monitoring across International Medical Affairs to strengthen governance and proactive risk management. You’ll shape monitoring frameworks, translate insights into actions, and drive sustainable operational excellence with cross-functional and cross-border impact. You will champion audit readiness, data-driven improvements, and responsible use of AI and digital tools to boost efficiency and consistency. This position offers high visibility to influence how Medical Affairs teams deliver priorities while upholding compliance and quality across geographies. You’ll join a culture that values transformation, governance Compensaciones / Beneficios • insurance plans, • retirement plans, • wellbeing resources, • global recognition programs, • flexible and hybrid working options, • minimum 14 weeks paid parental leave Responsabilidades, • Lead process effectiveness and first-line monitoring to ensure consistent, compliant execution, • Design and evolve monitoring frameworks to identify governance risks, trends, and improvement opportunities, • Translate monitoring insights into corrective and preventive actions, • Drive proactive risk management and address emerging governance and compliance risks, • Strengthen audit and inspection readiness with embedded processes and accountability, • Collaborate with country, regional, and functional stakeholders to improve adoption and operational effectiveness, • Lead process simplification and transformation initiatives while upholding governance standards, • Establish metrics to assess process effectiveness and prioritize improvements, • Champion the use of AI, analytics, and digital solutions to enhance monitoring and efficiency, • Lead and develop the Process Effectiveness and Monitoring team across geographies Requisitos principales, • Advanced degree in Medicine, Pharmacy, Life Sciences, or a related field, • Minimum 10 years of Medical Affairs, Quality and Compliance experience in the pharmaceutical industry, • Experience in international, regional, or above-country Medical Affairs roles within a complex global organization, • Experience leading multi-country first-line assurance including risk-based monitoring, quality oversight, internal controls, and CAPA management, • Experience translating enterprise standards into country practice, including audit and inspection readiness and cross-country remediation, • Experience defining performance and quality indicators and translating monitoring insights for senior leadership, • Previous people leadership experience with ability to develop and empower high-performing teams across geographies, • Excellent written and spoken English with strong communication, influencing, analytical, organizational, and stakeholder-management skills, • Influencing, • Stakeholder-management, • Analytical thinking, • Monitoring frameworks, • Risk management, • Quality and compliance

Alzheimer, impulsant la recerca biomèdica d'excel·lència i la sensibilització social.La nostra activitat científica es desenvolupa al.Barcelonaβeta Brain Research Center (BBRC).Alzheimer i altres malalties neurodegeneratives.La persona seleccionada tindrà un paper clau en el disseny i la gest

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.

In this AI transformation leadership role, you guide cross-functional teams to solve client challenges and deploy GenAI assets.You act as the bridge between client stakeholders, consulting teams, and technical delivery squads, ensuring alignment and delivering end-to-end programs.You drive AI-driven

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