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Busco una persona para ayudar en un traslado de mudanza en mi piso.Necesito mover muebles grandes, desmontar y volver a montar camas, y encajar cajas de libro y ropa en un camión o coche grande.Prefiero que la persona tenga experiencia en mudanzas, uso de furgoneta o coche grande, y conocimientos b

Fundació Pasqual Maragall busca un/a Research Project Manager para unirse al área de Strategic Research Funding. Se valorará experiencia en gestión de proyectos internacionales y conocimientos del entorno científico. La persona seleccionada participará en el diseño, gestión y seguimiento de convocatorias y proyectos, promoviendo cooperación entre instituciones y mejorando el impacto científico. #J-18808-Ljbffr

Clinical Research Associate IQVIA Spain is looking for talented and motivated team member to join our Sponsor dedicated team as junior 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, and build a meaningful, strong career within our organization. Your responsibilities will include: Performing site selection, initiation, monitoring and close-out visits Supporting the development of a subject recruitment plan Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions Collaborating with experts at study sites and with client representatives Qualifications: University degree in scientific discipline or health care Experience in Pharma Industry, and/or Clinical Trials environment Very good computer skills including MS Office Excellent command of Spanish and English language Organizational, time management and problem-solving skills Ability to establish and maintain effective working relationships with coworkers, managers, and clients Flexibility to travel Driver’s license class B What you can expect: Resources that promote your career growth Leaders that support flexible work schedules Programs to help you build your therapeutic knowledge Excellent working environment in a stabile, international, reputable company Mobile phone and attractive benefits package IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies. #J-18808-Ljbffr

Postdoctoral Researcher – Chromatin Biology Laboratory The Josep Carreras Leukaemia Research Institute (IJC) is a comprehensive cancer research center dedicated to the study of leukaemia and other hematologic malignancies. We are seeking a Postdoctoral Researcher for the Chromatin Biology Laboratory led by Dr. Alejandro Vaquero. RESEARCH DESCRIPTION The Chromatin Biology Laboratory focuses on the role of the Sirtuin family of enzymes in regulating genome stability and epigenetics under stress conditions, and their impact on cancer, senescence, and aging. MAIN RESPONSIBILITIES The successful candidate will explore the molecular and epigenetic mechanisms controlling the SIRT7/PAX5 interplay in B-cell differentiation and B‑Acute Lymphoblastic Leukemia (B‑ALL). The project utilizes a multidisciplinary approach, combining molecular and cellular biology techniques with genomics, proteomics, and metabolomics in mouse models and patient‑derived leukemia models. QUALIFICATIONS PhD in Biology, Biomedicine, Medicine, or a related discipline. Strong interest in cancer biology, especially the mechanisms underlying stress response, hematological malignancies, and immune regulation. Demonstrated experience with mouse models (essential), preferably in leukemia and/or sirtuin biology. Expertise in molecular and cellular biology techniques, including protein biochemistry, immunofluorescence, flow cytometry (FACS), and experience with proteomic and genomic approaches (essential). Previous experience in stress response pathways and/or sirtuin biology is highly desirable. Excellent communication, organizational, and teamwork skills. Excellent written and spoken English. BENEFITS 3‑year full‑time postdoctoral contract with potential one‑year extension following a positive evaluation. Full‑time contract (39 hours/week). Highly competitive salary. Exciting multidisciplinary research project with strong potential to advance B-cell acute lymphoblastic leukemia treatment. Collaboration with world leaders in clinical and pre‑clinical B‑ALL research and drug discovery. Opportunity to work in the outstanding multidisciplinary environment of the IJC. Stimulation of the Barcelona metropolitan area environment. DEADLINE Please submit your application by July 22nd, 2026. The IJC is an equal‑opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, national origin, disability, or other legally protected characteristics. #J-18808-Ljbffr

BCNatal | Fetal Medicine Research Center busca un/a Especialista en Monitoreo de Soportes Feto-salud para supervisar la experimentación animal y gestionar materiales de laboratorio. La posición exige formación universitaria en ciencias de la vida, disponibilidad para turnos y capacidad de trabajar de forma autónoma en un equipo multidisciplinar. Se valoran maestría relacionada, certificación animal y habilidades en gestión de muestras y datos. #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.Consulte la descripción del puesto a continuación. Si confía en que tiene las habilidades y la experiencia adecuadas, envíe su solicitud hoy mismo.You will identify funding calls, coordinate proposals, monitor outputs, and manage ethics and IP compliance, partnering with universities and industry to advance innovative projects. xqbhyrx Fluency in Spanish and Catalan, strong writing and negotiation skills, and a track record in higher education research administration are required.

Novartis in Barcelona, Spain is seeking a Lead Central Monitor to build and lead a high-performing team of Central Monitors.No espere a enviar su solicitud después de leer esta descripción; se espera un granvolumen de candidaturas para esta oportunidad.You will shape monitoring strategies across programs and Development Units, protecting patient safety, trial quality, and data integrity in a hybrid work setting.You will partner with clinical, data, and risk-surveillance teams to translate complex risk signals into actionable insights and to implement effective monitoring xqbhyrx and risk-mitigation approaches across globalHay opciones de teletrabajo/trabajo desde casa disponibles para este puesto.

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

• Preparar i impartir classes d’anglès a alumnes d’educació infantil i primària en el marc de les activitats extraescolars. - Dissenyar activitats lúdiques i pedagògiques adaptades a l’edat i nivell dels alumnes, fomentant l’aprenentatge natural de la llengua. - Potenciar la comprensió i expressió oral en anglès mitjançant jocs, cançons, contes i dinàmiques participatives. - Fer seguiment del progrés dels alumnes i adaptar les sessions a les seves necessitats i interessos. - Garantir un entorn segur, inclusiu i motivador per a l’aprenentatge.

Postdoctoral Researcher with experience in cognitive neuroscience Position Summary We are looking for a postdoctoral researcher with a PhD in Psychology, Biomedical Engineering, Neuroscience, or a related field to join our team at INAB (Instituto de Neurociencia Avanzada de Barcelona) in our Barcelona laboratories. INAB conducts research in cognitive neuroscience such as perception, consciousness, thinking, and emotions, so candidates with experience in these domains will be particularly valued. Responsibilities Design and develop experimental protocols for research projects. Process data from experimental recordings. Analyze data using advanced statistical and artificial intelligence techniques. Write and publish scientific articles in high-impact specialized journals. Present research findings at international conferences. Supervise and mentor postgraduate students. Requirements PhD in Psychology, Biomedical Engineering, Neuroscience, or a related field. Research experience in the fields of perception, consciousness, thinking, and emotions. Strong track record of writing and publishing scientific articles. Skills in experimental design and execution, as well as data processing. Advanced knowledge in statistics and data analysis. Experience supervising postgraduate students. Strong knowledge of experimental protocol design in research projects. Experience in one or more of the following techniques: Electroencephalography (EEG), Functional Near-Infrared Spectroscopy (fNIRS), Biosensors (ECG, GSR). Start Date and Conditions Start date: April-May 2026 in Barcelona. Competitive salary commensurate with experience and motivation. Opportunities for professional and academic development. Access to state-of-the-art facilities and equipment. How to Apply Interested candidates should send their curriculum vitae and contact information to info@inablab.org specifying the subject “Application for INAB postdoctoral researcher with experience in cognitive neuroscience”. Deadline by April 24th, 2026. About INAB The Institute of Advanced Neuroscience of Barcelona (INAB) is a newly established non-profit organization aimed at advancing new scientific models of the mind, brain, and human consciousness to promote a more aware, compassionate, and collaborative society. For further information:

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

Location : Barcelona - Spain (3 days working from the office and 2 days working from home) This is what you will do: The Associate Director, Global Health Economics & Outcomes Research (GHEOR) Analytics, develops and implements HEOR Analytics strategy, including conceptualizing real-world evidence studies, identification of data sources, study conduct and execution of publication plan. The incumbent will engage in hands on programming in R, python (or SAS if needed) and other programming languages or tools to efficiently work with real-world databases, to identify and discover target patient populations, describe treatment patterns, disease burden, health care resource utilization and cost, and other exploratory questions. The Associate Director is responsible to ensure that outcomes and quality data are produced to ensure the scientific medical standing of the potential value and real-world impact of Alexion products for payers, healthcare providers, and patients and caregivers. You will be responsible for: Designs and implements HEOR studies that support the clinical, economic, and patient centered value propositions, as well as reimbursement requirements for the therapeutic areas of interest. Manages analytics consultants and oversees the analysis activities by providing inputs to the analysis plans, monitoring the study conduct and reviewing study results. Provides statistical guidance or methodology and interprets the analysis results. Serves as a real-world data expert, identify data sources, and provide strategies to generate valid evidence from the appropriate databases. Provide new insights for disease area to help shape clinical development strategies and generates real world evidence for value decisions of therapies. Collaborates with Biostatistics team to work on clinical trial post-hoc analysis. Generates rapid real-world evidence to empower the development needs, speed up clinical trial design or facilitate quick decisions. Support preparation of medical or payer advisory meetings to solicit feedback on Alexion products and therapeutic areas specific disease impacts. Ensure quality and timely deliverables for all assigned studies/projects. Supports publication planning and execution, reviews, and approves abstracts or manuscripts. Participate in acquisition strategy for real-world data sources for possible in-license/ purchase and additional analytical tools for analytic needs. Contributes to the global HEOR analytics infrastructure, including develop best practices in HEOR Analytics function, identify areas for process improvement, and provide measures to improve quality and efficiency. You will need to have: BS/MS/MA in Statistics, Biostatistics, Computer Science, Mathematics and/or PhD in related area. Expertise in statistical methodologies including general linear models, multivariate regression, nonparametric methods, bayesian inference etc. 5+ years prior experience in data sciences/biostatistics, analytical programming using R, Python, SAS and other languages in the biopharmaceutical/pharmaceutical industry. Good understanding of the data structure and limitations of various types of real-world databases, and experience in working with large EMR or claims database are preferred. Experience with big data science, machine learning, AI models. Knowledge of clinical trials, and experience in analyzing and interpreting clinical trial data. Excellent written and oral communication skills Excellent presentation and interpersonal skills. Attention to detail while managing multiple projects under tight timelines. Flexibility and adaptability to internal and external changes. Experience and knowledge in rare disease is helpful, but not mandatory Date Posted 03-nov-2026 Closing Date 07-dic-2026 Alexion is proud to be an Equal Employment Opportunity and Affiliation. We are committed to fostering a culture of belonging where every single person can belong because of their uniqueness. The Company will not make decisions about employment, training, compensation, promotion, and other terms and conditions of employment based on race, color, religion, creed or lackthereof, sex, sexualorientation, age, ancestry, national origin, ethnicity, citizenship status, marital status,pregnancy, (including childbirth, breastfeeding, or related medical conditions), parental status (including adoption or surrogacy), military status, protected veteran status, disability, medical condition, gender identity or expression, genetic information, mental illness or other characteristics protected by law. Alexion provides reasonable accommodations to meet the needs of candidates and employees. Alexion participates in E-Verify. #J-18808-Ljbffr

Organisation/Company Universitat Autònoma de Barcelona Department Research Management/Strategic Projects Research Field Medical sciences » Epidemiology Researcher Profile Other Profession Positions Research Support Positions Application Deadline 31 Jul 2026 - 23:59 (Europe/Madrid) Country Spain Type of Contract Temporary Job Status Full-time Hours Per Week 35 Is the job funded through the EU Research Framework Programme? Horizon Europe Reference Number HORIZON-CL6-2025-02-FARM2FORK-02 Is the Job related to staff position within a Research Infrastructure? No Offer Description Job position Senior Research Support Technician Job position requirements (skills/languages/required experience)-Higher education degree (Bachelor’s or official Master’s).A degree in Applied Statistics and/or postgraduate studies related to data modeling will be valued -Knowledge of epidemiological analysis software such as R and QGIS -English Language -Previous experience in data analysis and epidemiology (risk analysis and multivariate analysis) Annual gross remuneration of €39.628,80 Eligibility criteria - Work experience in data analysis – 25 points ¿Está considerando presentar su candidatura para este trabajo? Compruebe todos los detalles en esta descripción del puesto y luego haga clic en "Solicitar".> 5 years: 25, 2–5 years: up to 24, < 2 years: up to 10 xhfqzwm - Experience in epidemiology (risk analysis) – 25 points > 5 years: 25, 2–5 years: up to 24, < 2 years: up to 10 Personal interview: 15 points Selection process A single curricular phase and if necessary, a second interview phase Programmes: HORIZON-CL6-2025-02-FARM2FORK-02 - SOA 35 - B-SAFE (Biosecurity for Sustainable Animal Farming in Europe) (OO5-2)#J-18808-Ljbffr

About Syneos Health CRA - Future Roles Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Every day we perform better because of how we work together, as one team, each the best at what we do. We bring a wide range of talented experts together across a wide range of business‑critical services that support our business. Every role within Corporate is vital to furthering our vision of Shortening the Distance from Lab to Life®. Discover what our 29,000 employees, across 110 countries already know. WORK HERE MATTERS EVERYWHERE We are passionate about developing our people, through career development and progression; A continuación,encontrará un desglose completo de todo lo que se requiere de los posibles candidatos, así como la forma de presentar su candidatura. ¡Mucha suerte! supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. Job Responsibilities Performs site qualification, site initiation, interim monitoring, site management activities and close‑out visits (performed on‑site or remotely) ensuring regulatory, ICH‑GCP and/or Good Pharmacoepidemiological Practices (GPP) and protocol compliance. Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site‑specific actions; immediatelycommunicates/escalates serious issues to the project team and with guidance develops action plans. Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes. Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient, as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/patient. Assesses factors that might affect subject/patient’s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. For the Clinical Monitoring/Site Management Plan (CMP/SMP): Assesses site processes, Conducts Source Document Review of appropriate site source documents and medical records, Verifies required clinical data entered in the case report form (CRF) is accurate and complete, Applies query resolution techniques remotely and on site, and provides guidance to site staff as necessary, driving query resolution to closure within agreed timelines, Utilizes available hardware and software to support the effective conduct of the clinical project data review and capture, Verifies site compliance with electronic data capture requirements. May perform investigational product (IP) inventory, reconciliation and reviews storage and security. Verifies the IP has been dispensed and administered to subjects/patients according to the protocol. Verifies issues or risks associated with blinded or randomized information related to IP. Applies knowledge of GCP/local regulations and organizational procedures to ensure IP is appropriately (re)labelled, imported and released/returned. Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness. Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator/physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations. Documents activities via confirmation letters, follow‑up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/Site Management Plan. Supports subject/patient recruitment, retention and awareness strategies. Enters data into tracking systems as required to track all observations, ongoing status and assigned action items to resolution. Manages site‑level activities/communication to ensure project objectives, deliverables and timelines are met. Must be able to quickly adapt, with the oversight of the Lead CRA, to changing priorities to achieve goals/targets. May act as primary liaison with project site personnel, or in collaboration with another CRA or Central Monitoring Associate (CMA). Ensures all assigned sites and project‑specific site team members are trained and compliant with applicable requirements. Prepares for and attends Investigator Meetings and/or sponsor face‑to‑face meetings. Participates in global clinical monitoring/project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according to the project specific requirements. Provides guidance at the site and project level towards audit readiness standards and supports preparation for audit and required follow‑up actions. For Real World Late Phase, the CRA I will use the business card title of Site Management Associate I. Additional responsibilities include: Site support throughout the study lifecycle from site identification through close‑out Knowledge of local requirements for real world late phase study designs Chart Abstraction activities and data collection Collaboration with Sponsor affiliates, medical science liaisons and local country staff. Qualifications Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience. Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements. Must demonstrate good computer skills and be able to embrace new technologies. Excellent communication, presentation and interpersonal skills. Ability to manage required travel of up to 75% on a regular basis. US ONLY: As part of your employment with Syneos Health, you may be deployed to sites that require certain medical and other personal information to gain facility access. Pursuant to our Employee Privacy Notice, Syneos Health can provide the sites with the information necessary for you to gain such access. Further, a site may ask you for additional information beyond that which Syneos Health has in its possession. You are required to comply with any such site requests as a condition of your employment with Syneos Health. We are always excited to connect with great talent. This posting is intended for a [possible] upcoming opportunity rather than a live role. By expressing your interest, you'll be added to our talent pipeline and considered should this role become available. Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever‑changing environment. Learn more about Syneos Health. Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. Summary Roles within Clinical Monitoring/CRA are responsible for overseeing and ensuring the integrity of clinical research studies by monitoring data and processes from a centralized location. This includes conducting remote monitoring of trial sites to verify compliance with regulatory requirements and clinical protocols. Utilizes data analytics and risk‑based monitoring techniques to identify potential issues and trends, ensuring that trials are conducted in accordance with established clinical practices. Collaborates with site teams to develop and implement tools, procedures, and processes that enhance quality monitoring and support the overall success of clinical trials. Impact and Contribution individual contributors with responsibility in a professional or technical discipline or specialty, but may manage two or fewer employees. May direct the work of lower level professionals or manage processes and programs. The majority of time is spent contributing to the design, implementation or delivery of processes, programs, and policies, using knowledge and skills typically acquired through advanced education. Entry to developing individual contributor. Delivers work of limited scope, typically smaller, less complex projects. xhfqzwm Requires theoretical knowledge of a professional area, typically obtained through education and/or prior experience. #J-18808-Ljbffr

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

The Germans Trias i Pujol Research Institute (IGTP) in Badalona near Barcelona hosts a GTS group focused on molecular characterization of Lewy body diseases.Consulte la descripción del puesto a continuación. Si confía en que tiene las habilidades y la experiencia adecuadas, envíe su solicitud hoy mismo.We seek a Research Technician with a Master’s to join an ambitious project investigating platelet-derived biomarkers for Lewy body disorders, including Olink data analysis and brain cell culture work.The successful candidate xqbhyrx will contribute to biomarker development, data interpretation, and manuscript drafting within a translational

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 dive

Inspired Education is the leading global group of premium schools, with a portfolio of 125 premium private schools spanning 6 continents which utilise proven educational practices from every corner of the globe, ensuring over 95,000 students receive a world-class learning experience from Kindergarten to Year 13. In 28 countries, Inspired schools are individually developed and anchored in the vibrant cultures of their respective locations. They collectively form an international family of schools that nurtures each student's academic and personal development in a progressive, dynamic, and innovative learning environment. By joining our award-winning team of over 14,000 employees, you can work in state-of-the-art facilities alongside industry-renowned educators and leaders in some of the world's most desirable locations. We invest heavily in our team members who enjoy industry-leading professional development, exceptional career opportunities, and mobility across our group. ROLE SUMMARY: The British College of Gava is seeking to appoint a dedicated and enthusiastic Primary Teacher to join our team on a temporary basis. We are looking for an inspiring educator who is passionate about delivering high-quality learning experiences and supporting children to achieve their full potential both academically and personally. KEY RESPONSIBILITIES: Plan, prepare and deliver high-quality lessons in line with the school's curriculum and educational standards. Create a stimulating, inclusive and supportive classroom environment. Monitor, assess and record student progress, providing constructive feedback to support achievement. Differentiate teaching strategies to meet the diverse needs of learners. Promote high standards of behaviour, engagement and wellbeing. Work collaboratively with colleagues on curriculum planning and school initiatives. Maintain effective communication with parents and carers regarding student progress and development. THE IDEAL CANDIDATE WILL HAVE: A recognised teaching qualification and relevant degree. Experience teaching within the Primary phase. Strong knowledge of effective teaching, learning and assessment practices. Excellent classroom management skills and the ability to create a positive learning environment. A commitment to delivering engaging and differentiated lessons that meet the needs of all learners. Excellent communication and interpersonal skills. The ability to build positive relationships with students, colleagues and parents. Strong organisational and time-management skills. SAFEGUARDING STATEMENT: Inspired Education Group is committed to safeguarding and promoting the welfare of children and young people and expects all staff, volunteers and other third parties to share this commitment. Safer recruitment practices and pre-employment background checks will be undertaken before any appointment is confirmed. Visit our careers site for more information; #J-18808-Ljbffr

Tipo de contrato INDEFINIDO CON PERIODO PRUEBA Responsabilidades Realizar acciones de formación a Farmacias, ECI y otros puntos de ventas, tanto de técnicas del productos como de tipo comercial para su venta, cubriento la zona de Cataluña y de forma puntual Andorra. Apoyo en eventos comerciales en punto de venta. Acciones de Dermoconsejera, sell out en farmacias. Valoración y recomendación de productos o tratamientos a profesionales o clientes. Promoción de marca en punto de venta. Realizar seguimiento de las necesidades de la zona asignada. Gestionar o resolver incidencia con clientes. Talleres de Productos y demostraciones en punto de venta. Venta y promoción de productos a cliente final. Ventajas sociales o económicas Vehículo empresa. Tarjeta Solred. Dtos. en productos compañía. Dto. en Seguro Salud Colectivo (Lo abona la persona trabajadora) Retribución variable en función de objetivos. Dietas y otros gastos de locomoción. Requisitos Estudios mínimos: Bachillerato. Cargo requerido: Visita Médica / Farmacias. Experiencia mínima: 3 años. Bachillerato o similar. Conocimientos en Venta / MKT. Conocimientos en Industria Farmacéutica. Se valora experiencia como Dermoconsejera. Obligatorio carnet de conducir automóviles. #J-18808-Ljbffr

Overview In this role you will steer consumer insights projects for telecom clients from kickoff to final presentation, shaping actionable marketing guidance. You’ll work within a global, multicultural team in Barcelona, delivering narrative-driven reports and compelling proposals. You’ll build client relationships to translate strategic goals into research objectives and mentor junior researchers. This position offers the chance to impact client decision-making through rigorous analysis and engaging storytelling. Responsabilidades • Manage end-to-end research projects from setup to delivery, • Design narrative-driven reports with actionable marketing insights, • Lead development of innovative proposals and pitches, • Develop deep client relationships to align research with strategic goals, • Oversee and coach junior research team members Requisitos principales, • 5+ years in consumer insights/research in a client-side (CMI) role within the Telecom industry, • Technical expertise in diverse consumer research methodologies and data collection/operations, • Strong knowledge of statistics and experience with statistical packages (Excel, SPSS, etc.), • Proven people management and motivational skills, • Excellent communication and stakeholder management experience, • Ability to solve problems and perform advanced data analysis in ambiguous environments, • Ability to work independently and under supervision, • Fluency in French (required); additional languages a plus, • Client-focused communication, • Leadership and mentorship, • Stakeholder management, • Research methodologies, • Data collection and operations, • Statistics

Dentro de Grupo Econocom, esta oferta es para Econocom Servicios. Revise detenidamente toda la documentación de la solicitud antes de hacer clic en el botón de solicitar al final de esta descripción.¿Eres experto/a en monitorización? ¿Te apasiona la IA? En Econocom Servicios buscamos incorporar un perfil de Administración de Monitorización y observabilidad con enfoque en IA con experiencia en plataformas de observabilidad y análisis para nuestro equipo de monitorización. Administrar, mantener y optimizar las plataformas de monitorización (CheckMK, Zabbix y Solarwinds) Diseñar y configurar nuevos checks, dashboards, alertas y umbrales. Visualización y Logs avanzados en Grafana. Desarrollo e implementación de flujos de trabajo basados en agentes autónomos de IA que ejecutan acciones basadas en razonamiento. Experiencia técnica directa implementando LLMs y consumiendo APIs de Claude (Anthropic) o similares y herramientas de código como Codex (no solo a nivel teórico, sino en entornos de producción). Scripting avanzado: dominio de Python orientado a la automatización de infraestructura, tratamiento de datos y scripting de sistemas. Desarrollo y consumo de APIs: acostumbrado a trabajar con APIs para realizar integraciones complejas entre diferentes plataformas. Orquestación y automatización de Flujos: experiencia práctica con N8N para la automatización de flujos de trabajo basados en nodos. Experiencia previa de al menos 3 años en administración de herramientas de monitorización. Experiencia en aplicación de IA en entornos de observabilidad y monitorización de infraestructura. Ámbito observabilidad: Conocimiento productos de monitorización On-Premise/Híbridos: experiencia avanzada en administración, configuración y despliegue de CheckMK, Zabbix y SolarWinds. Conocimiento productos de monitorización en Cloud: dominio nativo de telemetría, métricas y alertas en AWS CloudWatch y Azure Monitor. Visualización y logs avanzados: experiencia experta en todo el ecosistema de Grafana Labs (Grafana, Loki, Tempo) y el stack de Elasticsearch / ELK (Elasticsearch, Logstash, Kibana) para la correlación de eventos. Ámbito inteligencia artificial 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). Arquitecturas RAG (Generación aumentada por Recuperación): capacidad demostrada para diseñar y montar sistemas RAG Bases de datos vectoriales: experiencia técnica real configurando, indexando y optimizando Qdrant (u otras bases de datos vectoriales similares). IA agéntica: desarrollo e implementación de flujos de trabajo basados en agentes autónomos de IA que ejecutan acciones basadas en razonamiento. Ámbito automatización, scripting e integraciones: Scripting avanzado: dominio de Python orientado a la automatización de infraestructura, tratamiento de datos y scripting de sistemas. Desarrollo y consumo de APIs: acostumbrado a trabajar con APIs para realizar integraciones complejas entre diferentes plataformas. Orquestación y automatización de Flujos: experiencia práctica con N8N para la automatización de flujos de trabajo basados en nodos. Infraestructura como código (IaC) y operaciones: dominio de Ansible para la gestión de configuraciones y Rundeck como orquestador de tareas de operaciones (Runbook Automation). Ubicación: delegación de Barcelona (Carrer de l'Acer). Teletrabajo del 80%: un día de presencialidad en la oficina a la semana. Horario de lunes a viernes con hora de entrada entre las 8 y las 9. Opción de salario flexible. xhfqzwm Participación en proyectos de gran impacto y alta disponibilidad. #J-18808-Ljbffr

Work Schedule : Monday – Friday during regular business hours; Si está considerando enviar una solicitud, asegúrese de pulsar el botón de solicitar de abajo después de leer la descripción completa. Full-time Engagement Model : Fixed-term Employment Estimated Start Date : Early March 2026 DataForce by TransPerfect is seeking a UX Research Analyst to support ongoing user research initiatives for a temporary, full-time engagement. This role will focus primarily on operationalizing and managing questionnaire-based research studies, with an emphasis on Text-to-Speech (TTS) quality and potentially Translation quality. This is a hands-on, execution-focused role. The selected candidate will work closely with the client’s research team to administer studies, manage survey workflows, collect responses, and analyze results. The research design will be provided by the team; the analystwill ensurestudies are properly built, launched, monitored, and analyzed. Role Summary The UX Research Analyst will be responsible for implementing and managing questionnaire-based research studies from setup through reporting. This includes building surveys in Qualtrics based on predefined designs, configuring workflows and logic, monitoring live studies, ensuring data quality, and analyzing results. The role requires strong organizational skills and attention to detail to ensure studies run smoothly and findings are accurately documented and communicated to stakeholders. Role Responsibilities Build, configure, and manage questionnaire-based research studies using Qualtrics (or similar tools). Implement complex survey logic and workflows based on predefined study designs Launch and monitor studies to ensure smooth execution and data quality Collect, organize, and validate survey responses Analyze study results and prepare structured summaries of findings Collaborate directly with client stakeholders (East Coast US) on study execution and reporting Maintain documentation and ensure research processes are organized and repeatable Role Requirements 1–3 years of experience supporting or running questionnaire-based research studies Demonstrated experience collecting survey responses and analyzing results Strong working knowledge of Qualtrics, including survey logic and workflow configuration Fluent English (written and verbal) Strong organizational skills and attention to detail Ability to follow structured research plans and execute independently Preferred Role Requirements Experience in software, technology, or digital product environments Exposure to Text-to-Speech (TTS), voice testing, translation quality, or related domains Basic understanding of statistics for survey analysis Familiarity with user interfaces and UX concepts Experience working with distributed or international teams DataForce by TransPerfect is part of the TransPerfect family of companies, the world’s largest provider of language and technology solutions for global business, with offices in more than 100 cities worldwide. We offer high-quality data for Human-Machine Interaction to some of the most prestigious technology companies in the world. Our department focuses on gathering, enriching and processing data for Machine Learning in different AI domains. To learn more about DataForce please visit us at TransPerfect is an equal opportunity employer and committed to all recruitment processes and a workplace free from harassment, sexual harassment and discrimination. xhfqzwm For more information on the TransPerfect Family of Companies, please visit our website at #J-18808-LjbffrHay opciones de teletrabajo/trabajo desde casa disponibles para este puesto.

Part-time Research Assistant position in applied economics/political economy to assist with data collection, analysis, and field experiments, ideal for gaining research experience before a PhD.

Se busca un guía turístico en Barcelona para asistir a turistas, gestionar reservas y ofrecer una experiencia única, requerido nivel de japonés.

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 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)

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

IQVIA is seeking a Clinical Monitoring Analyst (Cluepoints) for a remote role, to support centralized monitoring activities across a sponsor project.Si cree que es el candidato ideal para la siguiente oportunidad, envíe su solicitud después de leer la descripción completa.Lead the setup, programming and refresh of the CM platform with strong SAS skills and clear stakeholder communication.Key responsibilities include CM strategy development, QTL/KRI/DQA implementation, and maintaining CM specifications.Excellent English communication and a solid data-management background are required. xqbhyrx Hay opciones de teletrabajo/trabajo desde casa disponibles para este puesto.

CTTC in Castelldefels is seeking a Researcher in the Communication Technologies Division–M2M Department to contribute to the FEMIOT project.¿Tiene su CV preparado? Si es así y confía en que este es el puesto ideal para usted, asegúrese de enviar su solicitud lo antes posible.The FEMIOT initiative, co-funded by FEDER, aims to advance telecom infrastructures for future smart cities and support connected and autonomous vehicles deployments.The successful candidate will engage in research activities related to machine-to-machine xqbhyrx communications within a European co-funded framework, collaborating with cross-disciplinary teams to

As a Sales Trainer, you will design and deliver impactful onboarding and skill development programs for both new hires and experienced team members to empower sales professionals. Your responsibilities will include: Develop and execute comprehensive training plans for new sales team members, designing and delivering engaging training modules covering product knowledge, objection handling, negotiation skills, and company best practices Assess training needs and create tailored learning plans and provide ongoing coaching and mentorship Evaluate training effectiveness and sales performance using feedback and key metrics collaborating with the managers and qualities to align the business needs Act as a subject matter expert on products and services and stay current on industry trends and emerging sales methodologies to continuously enhance training content Partner with cross-functional teams to identify training needs and share best practices and innovate and adapt training strategies to align with evolving business priorities and market conditions As a Sales Trainer, you will design and deliver impactful onboarding and skill development programs for both new hires and experienced team members to empower sales professionals. Your responsibilities will include: Develop and execute comprehensive training plans for new sales team members, designing and delivering engaging training modules covering product knowledge, objection handling, negotiation skills, and company best practices Assess training needs and create tailored learning plans and provide ongoing coaching and mentorship Evaluate training effectiveness and sales performance using feedback and key metrics collaborating with the managers and qualities to align the business needs Act as a subject matter expert on products and services and stay current on industry trends and emerging sales methodologies to continuously enhance training content Partner with cross-functional teams to identify training needs and share best practices and innovate and adapt training strategies to align with evolving business priorities and market conditions Requirements English level: C1 BA/BS degree or equivalent practical experience Hands-on sales expertise with a strong grasp of sales methodologies Experience designing and delivering sales training programs, preferably in software, SaaS, IT services, or system integration sectors is a plus Strong analytical skills, with the ability to assess learning outcomes and adapt programs accordingly Stakeholder management experience Desirable Skills Process Excellence: Systematically improving organizational processes to enhance efficiency, effectiveness, and quality Collaboration: Working effectively with others, sharing ideas and resources to achieve common goals Communication: Exchanging information, ideas, and messages between individuals or groups through various channels and mediums Emotional Intelligence: Understanding and managing one's own emotions and the emotions of others to foster positive relationships and enhance the impact of actions Open Mindedness: Considering and appreciating diverse perspectives and ideas, fostering collaboration Critical Thinking: Evaluating information and arguments, leading to informed and effective decisions based on data insights Solution Orientation: Approaching problems and challenges with a focus on finding practical and effective solutions Entrepreneurship: Having a mindset characterized by innovation, creativity, risk-taking, and a proactive approach to problem-solving and opportunity identification AI Proficiency: Understanding and leveraging Artificial Intelligence concepts, including machine learning, data analysis, and automation Data Literacy: Reading, interpreting, and analyzing data, enabling informed decision-making based on digital information Benefits This role offers significant exposure to cross-market leadership, B2B sales strategy, and marketplace growth, making it one of the most impactful career opportunities within TP Spain. Why Apply? Full-time (39 hours/week) position in Barcelona Competitive Salary Referral Program: Earn up to €2,000 for bringing friends, depending on the language/project Relocation package support You'll be based in Barcelona's 22@ district, a vibrant innovation hub where top global companies and international talent come together to create, grow, and lead Be at the forefront of a globally visible, high-growth initiative Opportunity to shape and scale a new sales-driven program Built-in expansion runway for rapid promotions and career development #J-18808-Ljbffr

Offer Description Revise detenidamente toda la documentación de la solicitud antes de hacer clic en el botón de solicitar al final de esta descripción. VHIR offers a position for a medical doctor specialising in cardiology in the Cardiac Imaging Unit within the Cardiovascular Diseases Research Group. We are a successful multidisciplinary group including cardiologists, technical researchers, radiologists and biostatisticians who work together to develop and implement advances in cardiovascular image analysis in clinical practice. We are seeking a Clinical Researcher to join our team. The main responsibilities of this role will be to annotate and validate echocardiograms, cardiac MRI scans and CT scans, include patients in various research projects, and contribute clinical expertise to the Cardiac Imaging Unit. Main responsibilities and duties Identification and inclusion of patients into the different research projects of the group Collection of clinical and demographic data and coordination of the performance of the various medical tests Clinical aspects related to bioengineering and data science work, including post-processing and analysis of different cardiac imaging studies. Strict collaboration with the technical researchers of the cardiovascular imaging unit. Fluency in Catalan, Spanish and English (business level) Specialisation in Cardiology Additional training in cardiac imaging Experience and knowledge Required: Relevant clinical experience as a medically qualified professional. Experience in participation in research lines and/or projects. Experience with cardiac imaging techniques (Echocardiography, Cardiac MRI and Cardiac CT). Proficiency in using digital tools and software for medical imaging. Research experience in cardiology or related fields Experience in scientific writing Experience presenting in conferences Note: Applicants may be required to provide evidence of their experience and achievements related to the requirements of the position during the application process through the ATS. Additional Information Incorporation into the Vall d’Hebron Research Institute (VHIR), a public sector institution that promotes and develops biomedical research, innovation and teaching at Vall d’Hebron University Hospital (HUVH), the largest hospital in Barcelona and the largest within the Catalan Institute of Health (ICS). A dynamic scientific environment of excellence , where cutting-edge biomedical projects are continuously developed. Continuous learning and career development pathways . 23 days of annual leave plus 9 personal days . Flexible remuneration programme , including meal vouchers, health insurance, transport and more. Corporate benefits platform , offering significant discounts on travel, culture, technology, gastronomy, sports and more. Healthy offering– “Feel Good, Feel VHIR” : VHIR’s wellbeing programme offers a variety of activities to help staff thrive—physically, mentally, and socially. Through four pillars—Feel Well, Feel Connected, Feel Empowered, Feel Welcomed—it fosters health, growth, and community. International mobility support (Welcome Services) : we aim to make your arrival in Barcelona smooth and pleasant by providing city information, guidance on required procedures, access to the International Welcome Desk, family support and assistance with finding accommodation. Selection process VHIR embraces Equality and Diversity. xhfqzwm As reflected in our values we work toward ensuring inclusion and equal opportunity in recruitment, hiring, training, and management for all staff within the organisation, regardless of gender, civil status, family status, sexual orientation, gender identity and expression, religion, age, functional diversity or ethnicity. Work Location(s) Number of offers available 1 Company/Institute Fundació Hospital Universitari Vall d'Hebron- Institut de recerca Country Spain Geofield #J-18808-Ljbffr

Monitors data center infrastructure, manages incidents, and ensures safety compliance.

Job Title Manager User Experience (UX) Research & Design Business Environment The Manager, UX Research & Design guides and develops a multi-disciplinary team delivering high-quality user experiences across Amadeus Hospitality products. This role shapes UX strategy, aligns research and design practices, supports the growth of UX maturity, and fosters effective collaboration with Product, Engineering, and business stakeholders. You will be responsible for supporting team performance, professional growth, and long-term capability development in alignment with user and business needs. Main Responsibilities UX Design & Strategy Provide strategic direction, constructive critique, and quality oversight to support high-quality design outcomes. Ensure alignment with user experience (UX) principles, accessibility standards, and the design system. Influence product scope and prioritization using research insights, data, and design frameworks. Project & Stakeholder Collaboration Promote early UX involvement across the full product lifecycle. Identify and plan for resource needs in alignment with product roadmaps and domain priorities. Collaborate with Product, Engineering, leadership, and customers to contribute to product direction and experience outcomes. UX Research Define and align on research strategy, guide methodologies, and ensure insights are actionable and credible. Increase visibility and understanding of UX research across product teams and leadership. Team Development & Coaching Encourage continuous learning, adaptability, and development within the team. Establish shared expectations, role clarity, and career paths for team members. Provide ongoing coaching, mentoring, and constructive feedback through regular one-to-one discussions. Support the development of competencies in research, design, communication, strategy, and cross-functional collaboration. Delegate thoughtfully and create opportunities for designers and researchers to take ownership of initiatives. The Ideal Candidate Bachelor's or Master's degree in Human-Computer Interaction (HCI), User Experience, Interaction Design, Psychology, Cognitive Science, Human Factors, Information Design, Computer Science, Business or Management, or a related field. Experience in User Experience, combining design, research, and cross-functional delivery. Experience guiding UX teams, including designers, researchers, writers, or design operations. Demonstrated experience contributing UX leadership in complex software-as-a-service (Saa S) environments, including business-to-business (B2 B), business-to-consumer (B2 C), or enterprise workflows. Experience designing for multi-platform ecosystems such as web, mobile, customer relationship management (CRM) platforms (e.G., Salesforce), or operational tools. Experience collaborating with product, engineering, and business partners to influence strategy and roadmaps. Skills & Competencies Advanced interaction and systems design skills, with experience using Figma or equivalent design tools. Solid understanding of information architecture, prototyping, usability testing, and accessibility best practices. Clear and effective communication, facilitation, and storytelling skills. Ability to work through ambiguity and engage senior stakeholders constructively. Understanding of design systems and how to scale user experiences across products. Collaborative approach and ability to work across geographies and disciplines. Clear ownership and accountability. Diversity & Inclusion Amadeus aspires to be a leader in Diversity and Inclusion in the tech industry, enabling every employee to reach their full potential by fostering a culture of belonging and fair treatment, attracting the best talent from all backgrounds, and as a role model for an inclusive employee experience. Amadeus is an equal opportunity employer and committed to an accessible recruitment process. All qualified applicants will receive consideration for employment without regard to gender, race, ethnicity, sexual orientation,age, beliefs, disability or any other characteristics protected by law. #J-18808-Ljbffr

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

• 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

En SEK International School Catalunya buscamos un profesor/a de PEP para incorporarse el 16 de diciembre.

The Josep Carreras Leukaemia Research Institute (IJC) is a comprehensive cancer research center dedicated to conduct research and drive innovation in the epidemiological, preventive, clinical, translational, and basic aspects of leukaemia and other hematologic malignancies, with the final aim of finding a cure for these diseases. It was created in 2010, and since then has experienced an exponential growth.The IJC is also part of the network of Excellence Research Centers of Catalonia (CERCA) and was accredited as a Severo Ochoa Center of Excellence by the Ministry of Science, Innovation, and Universities in 2024. Since 2018, the Institute has also been accredited by the Scientific Foundation of the Spanish Association Against Cancer (FCAECC) Additionally, IJC is one of the centers integrated into the Institut de Recerca Germans Trias i Pujol (IGTP) accreditation as Accredited Health Research Institute (IIS) by the Carlos III Health Institute (ISCIII).The IJC's main headquarters is located within the Can Ruti Biomedical Campus, alongside other leading biomedical institutions, providing direct access to cutting‑edge scientific and technological facilities, as well as complementary community services. The IJC has six locations integrated into reference hospitals: Hospital Germans Trias i Pujol, Hospital Clínic, Hospital Sant Pau, Hospital Josep Trueta, Hospital del Mar and Hospital San Joan de Déu. This facilitates close collaboration between basic and clinical researchers, fostering translational research that integrates basic science with clinical practice in clinical settings.We are looking for a Junior Postdoctoral Researcher for the Blood Stem Cell Identity group, led by Dr. Vincenzo Calvanese.RESEARCH DESCRIPTIONHematopoietic stem cells (HSC) are a life‑saving therapy for leukemia, and have found broadened applications in gene and cell therapy against other cancers, genetic, autoimmune, and infectious diseases. Yet practical limitations, such as donor‑matching or insufficient cell number, render these therapies unfeasible or unsuccessful for many patients. Attempts to overcome these limitations have been unable to create a reliable source of HSC for patients: while we can generate human HSC from pluripotent stem cells, they resemble early developmental stages, lacking many of the functional maturation hallmarks.The Postdoctoral Researcher will join the team to work on a project aimed at understanding the transcriptional and developmental mechanisms that govern the emergence, self‑renewal and maturation of human HSC, and their relevance for the establishment and maintenance of the leukemia stem cell population in the context of blood cancer. To dissect the nature and function of these cells, we combine directed differentiation of human pluripotent stem cells, in vitro and in vivo models of human normal and leukemic development, and state‑of‑the‑art epigenomic and transcriptomic profiling of cell lines and human primary tissues. This work will provide important advances in our understanding of human blood stem cell biology in the context of normal and neoplastic hematopoiesis.MAIN RESPONSIBILITIESDesign and perform cell culture assays and directed differentiation assays of hematopoietic stem cell sources including primary HSC (cord blood / bone marrow)Differentiation and culture of human pluripotent stem cells toward hematopoietic and endothelial fates, organoid assays and generation of iHSC or other hematopoietic lineages.Generate and characterize CRISPR‑Cas9 genome‑edited and fluorescent reporter pluripotent stem cell lines to track and interrogate developmental transitions.Perform cell surface marker analysis, cell enrichment and isolation by flow cytometry, MACS and FACS, and confocal/immunofluorescence imaging of normal and leukemic hematopoietic cells and tissues.Prepare samples and libraries for single‑cell RNA‑seq, spatial transcriptomics, and ATAC‑seq, and carry out downstream molecular biology (RNA/gDNA/cDNA, PCR, qPCR, Sanger sequencing).Perform in vivo assays of hematopoietic potential, including transplantation and analysis of immunodeficient mouse models.Coordinate with team members, bioinformaticians and collaborators to extract the maximum biological information from experiments and datasets, ensuring smooth communication and integration of expertise.Contribute to data interpretation and the preparation of clear, publication‑ready figures and presentation materials.Support and guide junior team members and students, fostering standardized and rigorous experimental approaches within the group.Maintain well‑organized records of protocols, samples and data, ready for internal and external use.Present research data within the team, across the institute and in collaborative settings, and disseminate project findings through talks and posters at national and international meetings; lead and contribute to the preparation of manuscripts for peer‑reviewed publication.Prepare and submit applications for competitive postdoctoral fellowships and complementary funding aligned with the scope of the project, in coordination with the group leader.WHAT WE NEEDPhD in Cell Biology, Developmental Biology, Stem Cell Biology or a related discipline.Strong hands‑on expertise in human hematopoietic and pluripotent stem cell culture and in vitro directed differentiation.Experience in genetic engineering (CRISPR‑Cas9, reporter line generation and characterization).Expertise in flow cytometry, FACS/MACS cell isolation, immunofluorescence and confocal imaging.Experience in functional hematopoietic assays (e.G. EHT, CFU) is highly desirable.Experience with sample and library preparation for single‑cell transcriptomics, spatial transcriptomics and/or ATAC‑seq.Solid molecular biology skills (RNA/DNA work, PCR, qPCR, sequencing).A background in hematopoiesis, stem cells, or tissue/cancer biology is highly desirable.Familiarity with basic bioinformatic analysis (e.G. R, Seurat for single‑cell RNA‑seq) is a plus, together with willingness to develop these skills further.A proven track record of peer‑reviewed publications, conference presentations, and collaborations.Strong motivation, excellent organizational skills, and the ability to work collaboratively and support team members.Excellent spoken and written English (please submit all documentation in English).Independent thinking, enthusiasm, pro‑activity, impeccable work ethics and professionalism. Commitment to an equity, diversity, and inclusion‑based, international working environment.WHAT WE OFFERPostdoctoral contract linked to the project "Overcoming the Epigenetic Drift in Culture‑Expanded Blood Adult Stem Cells", ATR2023‑143555, funded by MICIU/AEI (10.13039/501100011033).Full‑time contract (39 hours/week).Highly competitive salaryJoin a dynamic, international, multidisciplinary and forward‑thinking lab, recently established with the support of the EU (ERC‑CoG), Wellcome, FJC, and Spanish government funding.Work alongside a diverse and inclusive team of scientists at various training and experience levels, fostering mutual support, constructive feedback, and productive collaboration.The stimulating environment of the Barcelona metropolitan area.Contribute to pioneering research within the inspiring setting of the Josep Carreras Leukaemia Research Institute.DEADLINEDeadline: July 28, 2026.WHO WE ARE?What makes us different?The mission of the Josep Carreras Leukaemia Research Institute is to conduct research and drive innovation in the epidemiological, preventive, clinical, translational, and basic aspects of cancer, with a special emphasis on Leukaemia and other malignant blood diseases, with the aim of finding a cure for these diseases.The IJC’s vision is to be a world‑class reference and excellent research center that contributes to the improvement of results, and the cure of patients affected by leukaemia and other malignant haemopathies, through innovation, sustainability, social responsibility, talent, and professional experience.HR ExcellenceIn 2019, IJC was honored with the “Human Resources Excellence in Research Award” by the European Commission, recognizing the alignment of our human resources policies with the European Charter for Researchers and Code of Conduct for the Recruitment of Researchers. The Human Resources Strategy for Researchers (HRS4R) guides research centers of excellence in implementing and upholding these standards within their policies, emphasizing training, professional development, and mobility opportunities.The IJC’s commitment to these values and principles strengthens our internal policies and ensures that our members have the optimal conditions and environment for their professional development.The Board of Trustees is composed of representatives of the Generalitat de Catalunya (regional government), University of Barcelona, Autonomous University of Barcelona, the City of Badalona and the Jose Carreras International Leukaemia FoundationThe Catalan government provides hard money on an annual basis. The Jose Carreras International Leukaemia Foundation provides start‑up funds, project funds as well as financial support for investments.The JCI has an international scientific advisory board served by prominent researchers from US and Europe.The IJC has been awarded ERC and other EU grants.The IJC is an equal‑opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, national origin, disability, or other legally protected characteristics.#J-18808-Ljbffr

Profesores de ELEProfesores de MúsicaPrimeria, ESO y BachillerQueremos ofrecer las mejores alternativas a nuestros estudiantes a la hora de escoger su profesor/tutor para clases particulares, por ello, si eres profesor de cualquier asignatura en cualquiera de los niveles académicos mencionados est

About Syneos Health CRA - Future Roles Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Every day we perform better because of how we work together, as one team, each the best at what we do. We bring a wide range of talented experts together across a wide range of business‑critical services that support our business. Every role within Corporate is vital to furthering our vision of Shortening the Distance from Lab to Life®. Discover what our 29,000 employees, across 110 countries already know. WORK HERE MATTERS EVERYWHERE We are passionate about developing our people, through career development and progression; A continuación,encontrará un desglose completo de todo lo que se requiere de los posibles candidatos, así como la forma de presentar su candidatura. ¡Mucha suerte! supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. Job Responsibilities Performs site qualification, site initiation, interim monitoring, site management activities and close‑out visits (performed on‑site or remotely) ensuring regulatory, ICH‑GCP and/or Good Pharmacoepidemiological Practices (GPP) and protocol compliance. Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site‑specific actions; immediatelycommunicates/escalates serious issues to the project team and with guidance develops action plans. Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes. Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient, as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/patient. Assesses factors that might affect subject/patient’s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. For the Clinical Monitoring/Site Management Plan (CMP/SMP): Assesses site processes, Conducts Source Document Review of appropriate site source documents and medical records, Verifies required clinical data entered in the case report form (CRF) is accurate and complete, Applies query resolution techniques remotely and on site, and provides guidance to site staff as necessary, driving query resolution to closure within agreed timelines, Utilizes available hardware and software to support the effective conduct of the clinical project data review and capture, Verifies site compliance with electronic data capture requirements. May perform investigational product (IP) inventory, reconciliation and reviews storage and security. Verifies the IP has been dispensed and administered to subjects/patients according to the protocol. Verifies issues or risks associated with blinded or randomized information related to IP. Applies knowledge of GCP/local regulations and organizational procedures to ensure IP is appropriately (re)labelled, imported and released/returned. Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness. Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator/physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations. Documents activities via confirmation letters, follow‑up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/Site Management Plan. Supports subject/patient recruitment, retention and awareness strategies. Enters data into tracking systems as required to track all observations, ongoing status and assigned action items to resolution. Manages site‑level activities/communication to ensure project objectives, deliverables and timelines are met. Must be able to quickly adapt, with the oversight of the Lead CRA, to changing priorities to achieve goals/targets. May act as primary liaison with project site personnel, or in collaboration with another CRA or Central Monitoring Associate (CMA). Ensures all assigned sites and project‑specific site team members are trained and compliant with applicable requirements. Prepares for and attends Investigator Meetings and/or sponsor face‑to‑face meetings. Participates in global clinical monitoring/project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according to the project specific requirements. Provides guidance at the site and project level towards audit readiness standards and supports preparation for audit and required follow‑up actions. For Real World Late Phase, the CRA I will use the business card title of Site Management Associate I. Additional responsibilities include: Site support throughout the study lifecycle from site identification through close‑out Knowledge of local requirements for real world late phase study designs Chart Abstraction activities and data collection Collaboration with Sponsor affiliates, medical science liaisons and local country staff. Qualifications Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience. Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements. Must demonstrate good computer skills and be able to embrace new technologies. Excellent communication, presentation and interpersonal skills. Ability to manage required travel of up to 75% on a regular basis. US ONLY: As part of your employment with Syneos Health, you may be deployed to sites that require certain medical and other personal information to gain facility access. Pursuant to our Employee Privacy Notice, Syneos Health can provide the sites with the information necessary for you to gain such access. Further, a site may ask you for additional information beyond that which Syneos Health has in its possession. You are required to comply with any such site requests as a condition of your employment with Syneos Health. We are always excited to connect with great talent. This posting is intended for a [possible] upcoming opportunity rather than a live role. By expressing your interest, you'll be added to our talent pipeline and considered should this role become available. Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever‑changing environment. Learn more about Syneos Health. Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. Summary Roles within Clinical Monitoring/CRA are responsible for overseeing and ensuring the integrity of clinical research studies by monitoring data and processes from a centralized location. This includes conducting remote monitoring of trial sites to verify compliance with regulatory requirements and clinical protocols. Utilizes data analytics and risk‑based monitoring techniques to identify potential issues and trends, ensuring that trials are conducted in accordance with established clinical practices. Collaborates with site teams to develop and implement tools, procedures, and processes that enhance quality monitoring and support the overall success of clinical trials. Impact and Contribution individual contributors with responsibility in a professional or technical discipline or specialty, but may manage two or fewer employees. May direct the work of lower level professionals or manage processes and programs. The majority of time is spent contributing to the design, implementation or delivery of processes, programs, and policies, using knowledge and skills typically acquired through advanced education. Entry to developing individual contributor. Delivers work of limited scope, typically smaller, less complex projects. xhfqzwm Requires theoretical knowledge of a professional area, typically obtained through education and/or prior experience. #J-18808-Ljbffr

We are looking for a “Project Support to Research” to join IBEC in the frame of the project “Plataforma ISCIII Biomodelos y Biobancos” (PTC23/00002) within the call Plataformas ISCIII de apoyo a la I+D+I en Biomedicina y Ciencias de la Salud. The project is supported by the Instituto de Salud Carlos III. Main tasks and responsibilities / The successful candidate will develop research involving: Project Support to Research to oversee and give support to the research projects and activities within the Platform ISCIII of Biomodels and Biobanks. The extent of duties include: Liaising between project and funders; Obtenga más información sobre este puesto leyendo los detalles a continuación y luego envíe su solicitud para ser considerado. coordination between sites within international projects; coordinating and overseeing project reporting; keeping track of project agendas and deadlines. Assistance in identifying new project opportunities for the research lines assigned. Support in the definition of project goals, advising on project partners, preparation of budget, support on proposal writing and submission. Mange the outcome of the research lines within the available budget. Requirements for candidates: Bsc and Msc in Experimental Science or Biology. Demonstrable experience in management of projects Minimum 1 year of demonstrable experience in the framework of support research infrastructures at national and international level Minimum 1 year of demonstrable experience in biobank space backgrounds Full command of English. Competencies: Communication, teamwork, proactivity, customer orientation, planning and organizational skills. We Offer: Number of available positions: 1 Starting date: as soon as possible Working conditions: Full-time, fixed-term contract linked to the project “Plataforma ISCIII Biomodelos y Biobancos y Biomodelos, PTC23/0002” until 30/06/2027. Possibility of extension until December 2028 subject to new funding. Measures to reconcile work and family life (maternity and paternity leave, flexible schedule working hours, 23 working days of paid holidays, 9 leave days for personal matters, among others). IBEC ensures equality of access to professional development opportunities irrespective of employment status, length at IBEC or other factors. The IBEC’s yearly training catalogue offers a wide range of training in technical and transferable skills including mobility grants and a Mentoring programme. Stimulating, interdisciplinary research and high-quality international scientific environment. Induction programme to facilitate incorporation at IBEC and additional support is provided for foreigners to obtain Visa-working permit and to install in Barcelona. Reference: PSR-PTCEG If you have any further question regarding your application, please contact us at Principles of the selection process: IBEC 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) IBEC´s Commitment on equal opportunity, diversity, and Inclusion: Our strength and excellence as an international transdisciplinary Research Institute are based on diversity. Being an equal opportunity employer, we are committed to diversity and inclusion, so that we support employees irrespective of their gender, nationality, religion, disabilities, age, sexual identity or cultural and socioeconomic background. Visit our devoted webpage on Equality, Diversity and Inclusion. For candidates with children that come from outside Barcelona, we offer babysitting services during the interview, so you don’t have to worry about anything else than doing a good interview. Contact us if you are interested in this service. In categories where women are underrepresented, such as Group Leader positions, and with the aim of ensuring gender balance in recruitment processes, women candidates must represent at least 50% of those interviewed for Junior-level positions and 40% for Senior-level positions, provided they have CVs comparable to those of male candidates. At the end of the evaluation process, in cases of equal merit, preference will be given to women candidates. IBEC, as a signatory of the San Francisco Declaration on Research Assessment (DORA), will consider, especially for early-stage investigators, much more the scientific content of research outputs, than publication metrics or the identity of the journal in which it were published. Protection of personal data: IBEC guarantees that candidates’ personal data are processed in accordance with the requirements of the EU General Data Protection Regulation (GDPR) and Law 3/2018 on Data Protection. Personal data will be processed solely for the purposes of the selection process. Who we are? The Institute for Bioengineering of Catalonia, IBEC is an interdisciplinary research center focused on Bioengineering and Nanomedicine based in Barcelona. IBEC is one of the top research institutions named as a Severo Ochoa Research Centre by the Ministry of Science, Universities and Innovation, which recognizes excellence at the highest international level in terms of research, training, human resources, outreach and technology transfer. IBEC’s mission is to develop international high-quality interdisciplinary research that, while creating knowledge, contributes to making a better quality of life, improving health and creating wealth. A close link with key universities, reference hospitals and corporations, are assets that facilitate achieving the mission. IBEC was established in 2005 by the Generalitat de Catalunya (Autonomous Government of Catalonia), the University of Barcelona (UB) and the Technical University of Catalonia (UPC). xhfqzwm IBEC is located within the Barcelona Science Park and is managing 3.800 square meters facilities, with an annual budget of 22 Mio€; 4.150 square meters of facilities; 21 researchgroupsand a team of researchers and support services of 400 people from 35 different countries. #J-18808-Ljbffr

Associate Director, Global Health Economics & Outcomes Research Barcelona,, Spain Apply Now Find out how well you match with this jobA continuación, encontrará un desglose completo de todo lo que se requiere de los posibles candidatos, así como la forma de presentar su candidatura. ¡Mucha suerte!Associate Director, Global Health Economics & Outcomes ResearchThis is what you will do:The Associate Director, Global Health Economics and Outcomes Research (GHEOR) leads the strategic development and execution of health economics and outcomes research strategies and deliverables to support the worldwide launch and reimbursement of products across a range of multiple disease areas, assets, and indications.Through key leadership and partnership (including Global Value, Access & dical, Research & Development, Regulatory, Commercial, etc.), the job holder embeds global HEOR strategy into broader disease area and clinical development strategies.This collaboration builds strategies to demonstrate and differentiate the value proposition and corresponding scientific evidence of Alexion products for payers, patients, clinical institutions, and other key decision makers.You will be responsible for:Utilizing in-depth knowledge of disease area and portfolio strategy in combination with health economics and outcomes research to develop and execute the Global HEOR strategy.Ensures payer relevant endpoints and evidence generation strategies are implemented throughout the product lifecycle.Accountable for the following: Builds collaborative relationships with cross-functional leaders across Research & Development, Commercial, Medical, Market Access organizations to maximize evidence generation efforts to optimize launch and sustained reimbursement of multiple indications or medicines throughout the product lifecycle Partners with the Therapeutic Area (TA) heads to develop TA business strategies and clinical development plans that will provide a competitive advantage to differentiated payer evidence; drives efficient and innovative HEOR study development and study execution and dissemination. Continually monitors the global marketplace for market access issues and creates plans to demonstrate the value and differentiation of assets within the therapeutic area portfolio.Ensures Alexion maintains external credibility and relationships to validate research findings and communications.Accountable for the following: Cultivates and maintains relationships with key experts, influencers, and customer segments to foster and maintain Alexion’s credibility to support the value and reimbursement of Alexion products Delivers presentations on behalf of Alexion at various industry and scientific forums and/or lead/contribute to publications Maintains the relationship with external agencies and monitors their performance to ensure that performance and deliverables meet business expectations Contributes to the global HEOR infrastructure to provide direction and guidance to Regional HEOR teams.Accountable for the following: Develops best practices in HEOR including approaches to areas including research methodologies, economic modeling, study designs, endpoints that provide scientifically sound protocols, policies, tools, and outcome impact. Provides global oversight and guidance to country teams to adapt the global strategies into tactical plans through robust Health Technology Assessment processes to achieve optimal access and sustained reimbursement throughout the product lifecycle.* Identify areas for process improvements, economies of scale, and other quality and efficiency measures.You will need to have: Ph D or equivalent combination of education and experience with Pharmacy or clinical as domain knowledge 5+years prior experience in HEOR or Market Access in the biopharmaceutical/pharmaceutical industry Thorough understanding of the field of Health Technology Assessment at a global level and experience of successful negotiations through the HTA processes Understanding of the global market access landscape and the US health care environment Knowledge of the drug development and commercialization process Recognized as a strong leader with a proven track record of effectively influencing, and developing people including those who are not direct reports: demonstrated ability to lead and deliver results in a matrix environment, and solve complex issues that cross multiple stakeholders Excellent interpersonal skills with a track record of effectiveness as a team player; excellent oral/written communication and presentation skills Excellent project leader who can effectively manage multiple competing priorities to completion Positive team player with a Global mindset and ability to work with multicultural teams Flexibility and adaptability to internal and external change Financial accountability and budget management Demonstrates high business ethics/integrity and delivers research projects with high quality Published research in reputed journals The duties of this role are generally conducted in an office environment.As is typical of an office-based role, employees must be able, with or without an accommodation to: use a computer; engage in communications via phone, video, and electronic messaging; engage in problemsolving and non-linear thought, analysis, and dialogue; collaborate with others; maintain general availability during standard business hours.We would prefer for you to have:Experience and knowledge in rare disease conditionsDate Posted27-jul-2026Closing Date09-ago-2026 Alexion is proud to be an Equal Employment Opportunity and Affirmative Action employer.We are committed to fostering a culture of belonging where every single person can belong because of their uniqueness.The Company will not make decisions about employment, training, compensation, promotion, and other terms and conditions of employment based on race, color, religion, creed or lack thereof, sex, sexual orientation, age, ancestry, national origin, ethnicity, citizenship status, marital status, pregnancy, (including childbirth, breastfeeding, or related medical conditions), parental status (including adoption or surrogacy), military status, protected veteran status, disability, medical condition, gender identity or expression, genetic information, mental illness or other characteristics protected by law.Alexion provides reasonable accommodations to meet the needs of candidates and employees. xlqxfvg To begin an interactive dialogue with Alexion regarding an accommodation, please contact Alexion participates in E-Verify.#J-18808-Ljbffr

Employment Type: Full Time (35 hours per week) Duration: Continuing Remuneration: Level B $133,065 - $156,864 (depending on experience) + 17% super + leave loading Location: UNSW Kensington Campus This Job is based in Australia Research Fellow About Us The UNSW Centre for Social Impact (CSI) is an education and research centre based at UNSW Business School. Our mission is to develop people and partnerships that accelerate social innovations that build the impact economy. Through engaged scholarship, we work collaboratively with communities, organisations and governments to address complex social and environmental challenges and create practical solutions that contribute to social impact. We are part of UNSW Business School, a top business school in the Asia–Pacific region, with a global reputation for innovation, research excellence and teaching that embeds real business and community challenges into curricula. At our core are exceptional academics and researchers, alongside students dedicated to advancing social, economic and environmental progress for future generations. Position Summary A Research Fellow (Level B) is a valued member of the research team, and expected to carry out both independent and collaborative research that supports the CSI research strategy pillars of investment, innovation, and strategy and evaluation of social impact. They will produce both academic and practitioner outputs from research projects, diffusing knowledge to ensure it contributes to economic and social prosperity. The Research Fellow reports to the Research & Innovation Director and has no direct reports. A current focus of the role will be participating in and supporting Chief Investigators of an Australian Research Council Discovery Project investigating the strengthening of regional economies through place-based investment. Key Responsibilities Conduct research/scholarly activities under limited supervision, either independently or as a member of a team. Create scholarly impact in the discipline which is recognised by peers in the advancement of disciplinary knowledge, including high-quality academic publications and public contributions Contribute to the strategy of the Centre of Social Impact, through the design and development of applications for competitive funding for research Participate as co-investigator or chief investigator in competitive grant applications, or show evidence of active participation in research collaborations funded by competitive grants. Support the dissemination of research outcomes through appropriate channels and outlets. Undertake research activities and field work, e.G. surveys, literature reviews, data gathering (including interviewing) and/or recording of results using appropriate research methods. Participate in and/or present at conferences and/or workshops relevant to projects as required. Assist with the supervision of research students and assistants in the research area where required. Provide leadership and support for project management and administration to achieve deliverables, including organising and attending place-based focus groups and meetings with participants. Skills And Experience A Ph D in a business-related discipline, including management, organisation studies, strategy, entrepreneurship, and sociology, with expertise in qualitative and mixed methodologies Proven commitment to proactively keeping up to date with discipline knowledge and developments, especially relevant to impact investing, regional economic development, and/or civic wealth creation. Demonstrated track record in research with outcomes of high quality and high impact with clear evidence of the desire and ability to continually achieve research excellence as well as the capacity for research leadership. A track record of significant involvement with the profession and/or industry in conducting research projects with academic and industry relevant outcomes. High level communication skills and ability to network effectively and interact with a diverse range of students, staff, industry, and community partners Demonstrated ability to work in a team, collaborate across disciplines and build effective relationships, especially with external partners. Evidence of highly developed interpersonal and organisational skills. For further details on role responsibilities and skills & experience required, refer to the position description found under the position listing on Jobs@UNSW Please note: Sponsorship is not available for this role, valid Australian working rights are required on application. Pre-Employment Checks As part of our recruitment process candidates may be required to undergo pre-employment screening, which may include reference checks, qualification verification, right-to-work verification, and criminal history screening where relevant to the role. UNSW is committed to equity diversity and inclusion. Applications from women, people of culturally and linguistically diverse backgrounds, those living with disabilities, members of the LGBTIQ+ community; and people of Aboriginal and Torres Strait Islander descent, are encouraged. UNSW provides workplace adjustments for people with disability, and access to flexible work options for eligible staff. The University reserves the right not to proceed with any appointment.

Estem buscant monitor/monitora de menjador a les nostres escoles públiques situades a Barcelona. Competències / coneixements: Títol de monitor/a de lleureCompetències:- Analitzar i resoldre problemes- Iniciativa y autonomía- Comunicació interpersonal- Treball en equip- Proactivitat- Empatia- C

Carrerasresearch is seeking a Predoctoral Researcher for the 3D chromatin organization group led by Dr. Biola M. Javierre. This position offers an opportunity to work on innovative research within the Josep Carreras Leukaemia Research Institute, focusing on the role of regulatory elements in hematological malignancies.Ideal candidates will possess a Master’s degree in Bioinformatics or Biomedical Sciences, with strong expertise in computational biology and a motivation for a research career. The role involves collaboration in a dynamic environment, contributing to critical research aimed at fighting cancer.#J-18808-Ljbffr

Se busca monitor/a de tiempo libre para acompañar a niños en el transporte escolar, asegurando su bienestar y seguridad.

The Mobile Robotics research line of the Robotics and Automation Unit at Eurecat Technology Center (Barcelona) is seeking a SLAM & Autonomous Navigation Researcher with a strong background in robotics software, localization, mapping and autonomous navigation, together with hands-on experience de

Seeking an elite English conversational partner for intensive corporate language training, requiring bilingual proficiency and teaching experience for a 3-year commitment.

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