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IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world. Learn more at https://jobs.Iqvia.ComIQVIA Safety Operations team play an important part in the design, build and execution of end-to-end safety solutions for major pharmaceutical companies and their post market products around the world. We are proud to be an international, diverse team based across the world, with 'safety hubs' in Ireland, Poland, Austria, Portugal, Slovakia, Spain, India and USA. Each new joiner is supported by a nurturing management team, collaborative colleagues as well as a clear career ladder with plenty of opportunities to allow you to grow, adapt and shine.Medical Information Specialist with Dutch, French and English.This position will put you at the forefront of Patient Safety. With daily direct contact with Health Care Professionals (HCPs) and patients (the very people we are working to help), this is a highly visible and important role within IQVIA and essential to our core goal of patient safety. You will perform key medical information call center services and process safety and product quality information to help optimize the safety profiles of products across various therapeutic areas: Respiratory; Infectious diseases, Immunology and Inflammation; HIV & Oncology.You willbenefit from joining the largest safety department in the world and working within an industry-leading, best-practice environment. To ensure you contribute to the business and grow your career, you will also benefit from ongoing training and development from our in-house safety experts to plan and progress your career.RESPONSIBILITIES- Provide phone support to health care professionals and patients, involving receipt and tracking of medical inquiries, adverse events, product quality complaints, and other types of calls as required.- Receive and document incoming telephone calls, faxes or emails from various sources including investigative sites during regular weekday business working hours.- Establish and maintain effective team communications i.E. provide regular feedback to the local management team on project metrics, out of scope work challenges/issues and successes.- Build a positive, collaborative team environment with other Lifecycle safety team members.- Participate in training across Lifecycle safety service offerings, participate in working groups as applicable in implementation of new initiatives, identification, and implementation of process efficiencies.REQUIRED KNOWLEDGE, SKILLS AND ABILITIES- Bachelor's Degree in a Life Science is required. .- Excellent written and verbal skills in Dutch (native/C2), French (min. C1) and English (min.C1)- Willingness and aptitude to learn new skills across our Lifecycle Safety service lines.- Excellent attention to detail and accuracy maintaining consistently high-quality standards.- Excellent organizational skills and time management skills.- Ability to establish and maintain effective working relationships with coworkers, managers and clients.- Ability to work effectively on multiple projects simultaneously, organize own workload and effectively manage competing priorities.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

IQVIA Argentina is looking for an Associate Principal to drive mixed-methods research and implementation science. This hybrid role involves scientific leadership in a multidisciplinary environment, focusing on project delivery and client engagement.The ideal candidate should possess an advanced degree and extensive experience in survey design and mixed-methods research, along with strong writing and presentation skills. Join IQVIA in transforming patient experiences and healthcare solutions.#J-18808-Ljbffr

IQVIA is seeking an HTA Analyst to support UK HTA submissions and engagement with agencies such as NICE and the SMC. The role offers flexibility for office and home working across Spain, with opportunities to grow into senior HTA positions within the team.You will work flexibly across HEOR projects, developing strategic HTA knowledge and collaborating with internal IQVIA teams to deliver high-quality evidence.#J-18808-Ljbffr

Aim high, go beyond!At Open Cosmos we are solving the world’s biggest challenges from space, providing businesses, governments and researchers access to more readily available information than ever before - ready for the challenge? Then read on…Working in our Data DivisionAt Open Cosmos, our Data division transforms satellite data into meaningful insights that drive real-world impact. The team delivers all data products generated by Open Cosmos and its partners, curates and develops DataCosmos (our geospatial data platform) and builds integrations that make satellite imagery easy to access and act on.The team is now looking for an Image Production Engineer to join the growing team!What will you be doing?As an Image Production Engineer, you’ll own the end-to-end imagery processing pipeline, ensuring satellite data is transformed into high-quality, reliable, and actionable outputs for customers around the world.You will:- Own and continuously improve the imagery pipeline from acquisition to delivery- Ensure quality, reliability, and performance meet KPIs and customer expectations- Identify and fix issues, bottlenecks, and failure points across the system- Define data quality standards and implement robust validation and monitoring- Work closely with engineering and SRE to keep systems scalable and resilient- Troubleshoot and improve production code (Python) where needed- Drive automation and performance improvements across the pipeline- Support customer delivery and success through consistent, high-quality outputsWhat You’ll bring- Ownership of data or imagery pipelines end-to-end, from acquisition through to delivery- Strong problem-solving ability with the ability to get to root cause and fix issues properly- Confidence working with Python in production environments- Solid understanding of remote sensing and satellite imagery processing- Ability to build and apply monitoring, validation, and performance optimisation approaches- A mindset of ownership, curiosity, and continuous improvementThis role can be based in UK (Harwell, Oxfordshire) | Spain (Barcelona) | Portugal (Porto) | Greece (Athens) or Argentina (Buenos Aires)To apply, you must have the legal right to work in our chosen location.When applying, please submit your CV in English.Why Open Cosmos?- Work at the cutting edge of space technology with customers around the globe.- A mission-driven company making space accessible to help solve real-world challenges.- A diverse, ambitious, and supportive team.#J-18808-Ljbffr

Join us on our exciting journey!IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics, and human ingenuity to drive healthcare forward.Sales Executive, Life Sciences, Safety Technology, EMEAIQVIA's Safety Technology business is transforming pharmacovigilance through innovative, AI-powered solutions that help life sciences organizations improve patient safety, streamline operations, and accelerate decision-making. Our end-to-end safety platform combines advanced analytics, machine learning, natural language processing, and generative AI to automate case processing, detect adverse events, and provide real-time safety insights across the product lifecycle.As a Sales Executive, Life Sciences, Safety Technology, EMEA, you will play a key role in driving growth across our Safety portfolio, partnering with pharmaceutical, biotechnology, medical device, and clinical research organizations. You will engage senior safety leaders to understand their business challenges and position IQVIA's market-leading pharmacovigilance technology, analytics, and managed service solutions to improve efficiency, compliance, and patient outcomes.This is a high-impact, strategic sales role for an experienced enterprise software professional with a strong track record of selling complex SaaS, technology, and services solutions within the life sciences industry. Working across the EMEA region, you will collaborate closely with product, consulting, and delivery teams to help customers modernize their safety operations and unlock the value of AI-driven pharmacovigilance.Responsibilities- Develop new business by prospecting accounts focused on Drug Safety and Pharmacovigilance solutions, consulting services, hosting, and managed services.- Meet or exceed annual quotas by identifying and developing new accounts, following up on existing leads, and generating both incremental and repeatable business.- Develop and maintain productive relationships with key target accounts.- Work collaboratively with Product, Professional Services, Hosting, and Managed Services teams to ensure successful delivery of safety solutions and to develop client-centric offerings.- Identify and respond to customer needs to define opportunities for Pharmacovigilance and Drug Safety solutions, proposing tailored solutions aligned with client requirements.- Manage assigned strategic and key account relationships individually or in coordination with Global and Regional Sales teams.Requirements- Demonstrated success selling enterprise solutions, consulting services, hosting, and managed services to Pharmaceutical, Biotech, Medical Device, and Clinical Research Organizations, with a strong focus on Drug Safety and Pharmacovigilance.- Proven experience managing relationships with senior stakeholders in a fast-paced growth environment.- Full sales cycle experience: prospecting, opportunity identification, solution development, proposal creation, negotiation, and closing.- Strong written and verbal English communication skills.- Ambitious, driven, self-motivated, and adaptable to a high-growth sales environment.- Bachelor's degree or equivalent experience.- Willingness to travel across EMEA as required.Highly preferred capabilities:- Strong understanding of the pharmacovigilance and drug safety lifecycle, including pre-market and post-market activities.- Experience selling drug safety technology, pharmacovigilance services, case processing solutions, signal detection solutions, safety analytics, hosting, and managed services.- Experience engaging with Heads of Safety, Global Safety Leaders, Chief Medical Officers, Pharmacovigilance Operations Leaders, and Safety Systems stakeholders.- Proven success in a Software-as-a-Service (SaaS) environment.- 10+ years of experience in sales, business development, or a related commercial role.Why Join?You can drive your career at IQVIA and choose the path that best defines your development and success. With exposure across diverse geographies, capabilities, and vast therapeutic and information and technology areas, you can seek opportunities to change and grow without boundaries.We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes.It's an exciting time to join and reimagine what's possible in healthcare.Moving healthcare forward. Together.IQVIA is a strong advocate of diversity and inclusion in the workplace. We believe that a work environment that embraces diversity will give us a competitive advantage in the global marketplace and enhance our success. We believe that an inclusive and respectful workplace culture fosters a sense of belonging among our employees, builds a stronger team, and allows individual employees the opportunity to maximize their personal potential.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.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

IQVIA is hiring a Medical Information Specialist with Dutch, French and English to support health care professionals and patients. The role centers on safety data handling, medical information inquiries, and product quality information to optimize safety profiles across therapeutic areas.The position offers training from safety experts and a clear career ladder within IQVIA's safety organization, with opportunities to grow in a global, diverse team across safety hubs worldwide.#J-18808-Ljbffr

¡Buscamos Change Manager (P2 P) en Barcelona! ¿Buscas unirte a un entorno dinámico e internacional donde el impacto de tu trabajo sea visible a escala global? En Extia, nuestro lema es “First who, then what” (Primero la persona, después el proyecto). Priorizamos a las personas y al trabajo en equipo para ofrecer soluciones de gran impacto. Como el 1.º Great Place To Work® Francia 2024-25 y Great Place To Work® Europa por séptimo año consecutivo, estamos convencidos de que el bienestar en el trabajo impulsa el rendimiento. Buscamos un/a Change Manager para liderar la estrategia de gestión del cambio en el despliegue internacional de una solución Procure-to-Pay (P2 P) en varios países de Latinoamérica (Colombia, México y Argentina) y futuras olas en Europa. Trabajarás con autonomía coordinando equipos globales y locales de compras, facturación y gestión de proveedores, garantizando la adopción exitosa de los nuevos procesos y herramientas. Misión y Responsabilidades Principales Estrategia y Plan de Cambio: Definir, actualizar y mantener la estrategia global de Change Management, elaborando los planes de comunicación, formación y preparación del negocio (business readiness). Gestión y Seguimiento de Proyecto: Definir y coordinar entregables, realizando un seguimiento semanal de acciones para asegurar el cumplimiento de hitos en despliegues multipaís. Comunicaciones y Formación: Diseñar y adaptar materiales comunicativos y formativos, coordinando su distribución a través de los equipos locales y gestionando los datos de capacitación. Gestión de Resistencias e Stakeholders: Identificar tempranamente barreras al cambio, resolver objeciones y actuar como interlocutor clave entre la alta dirección y los equipos operativos locales. Soporte al Go-Live y Hypercare: Acompañar a las filiales en las fases críticas del lanzamiento y post-lanzamiento para asegurar una transición fluida y la estabilización del proceso. Experiencia en Change Management: Trayectoria sólida liderando planes de cambio organizativo en el ámbito de Procure-to-Pay (P2 P), compras, facturación o gestión de proveedores. Entornos Multinacionales: Experiencia previa trabajando en compañías globales y coordinando proyectos transversales en múltiples países de forma independiente. Gestión de Proyectos: Excelente habilidades de organización, documentación y reporte para el seguimiento continuo de entregables técnicos y operativos. Idiomas: Dominio fluido de Inglés y Español (imprescindible para la interlocución con stakeholders internacionales y locales). Habilidades Relacionales: Gran capacidad de comunicación oral/escrita, orientación a soluciones y facilidad para mitigar resistencias al cambio. Herramientas P2 P/ERP: Experiencia previa con soluciones como Coupa, SAP o People Soft. Metodologías: Conocimiento y trabajo bajo marcos de trabajo Agile. Conocimiento de Entornos Europeos: Familiaridad con requerimientos de Comités de Empresa (Work Councils) y normativas locales para futuras fases en Europa. ¿Por qué unirte a Extia? Flexibilidad real – Modelo adaptado a tu proyecto y equilibrio vida personal/profesional Triple Seguimiento – Un Coach, un Manager y un HR siempre a tu lado Paquete de beneficios competitivo – Seguro Médico (incl. Fisioterapia y Psicología) + Ticket Restaurante + Transporte Entorno internacional – Más de 3.000 colaboradores en Europa y Canadá Great Place to Work – Cultura basada en cercanía, transparencia y acompañamiento real Eventos, afterworks y comunidad activa – Team buildings, acciones solidarias, meetups, celebraciones internas… ¡Nos gusta compartir más allá del trabajo! En Extia creemos en “Primero quién, luego qué”. Si te motiva liderar proyectos de gestión del cambio a escala global, queremos conocerte #J-18808-Ljbffr

IQVIA is seeking a Lead Medical Writer to oversee a range of writing projects, ensuring SOP compliance and timely delivery. You will lead senior reviews, negotiate timelines with customers, and guide project teams.You will provide feedback to junior staff, stay current with GCP and regulatory knowledge, and may lead meetings or training for the global team. A strong track record in medical writing and leadership is essential.#J-18808-Ljbffr

IQVIA seeks a Senior Patient Recruitment Manager to coordinate recruitment and retention programs for small to mid-size studies across internal teams and external providers. You will oversee budgets, timelines, and KPI performance, working with sponsors and project teams to optimize study outcomes.The role requires deep knowledge of drug development, GCP/ICH guidelines, and strong leadership in a global client-facing environment.#J-18808-Ljbffr

IQVIA is seeking a Senior Statistical Programmer to review and prepare ADaM datasets, tables, figures, and listings for submission. You will design, develop and QC SAS programs used to access, transform, review and analyze CDISC-compliant data across studies.You will collaborate with study statisticians and clinical programming teams, lead in-house data delivery, and support regulatory activities and publications with a focus on quality and timeliness.#J-18808-Ljbffr

Associate Principal - Mixed Methods Research: Patient Experience - Home-based/HybridBarcelona, Spain | Full time | Hybrid | R1536610Associate Principal, Implementation Science & Mixed Methods ResearchIQVIA is The Human Data Science Company, focused on using data and science to help healthcare clients find better solutions for their patients. IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics, and human ingenuity to drive healthcare forward.Patient Centered Solutions (PCS)The Patient Centered Solutions (PCS) team leads the industry in the science of measuring the patient and stakeholder experience. PCS combines strategic consulting expertise with rigorous scientific methods to design and execute mixed-methods, survey-based, and implementation science research that informs development, access, and real-world use of medical products and healthcare interventions.Role overview and responsibilities focus on hands-on scientific leadership, project delivery, and growing external visibility in a global, multi-disciplinary setting.Role OverviewAssociate Principal will serve as a senior subject matter expert in mixed-methods research, survey science, and implementation science, supporting client delivery, business development, external thought leadership, and internal capacity building across the organization. This role emphasizes hands-on scientific leadership, project delivery excellence, and growing external visibility.Key ResponsibilitiesClient Delivery & Scientific Leadership- Serve as a senior scientific contributor and subject matter expert on client projects involving mixed-methods research, survey studies, and implementation science methodologies.- Lead or co-lead study design, instrument development, qualitative and quantitative analysis, and interpretation of findings.- Ensure methodological rigor, alignment with best practices, and fit-for-purpose study designs across therapeutic areas.- Review and contribute to key scientific deliverables including protocols, analysis plans, reports, manuscripts, and client presentations.Survey Science & Mixed-Methods Expertise- Provide expertise in survey design, item development, response scaling, cognitive testing, and item reduction.- Apply mixed-methods approaches to integrate qualitative and quantitative findings in a coherent and decision-oriented manner.- Support development and refinement of implementation-focused measures, including barriers, facilitators, and outcome constructs.Implementation Science Application- Apply implementation science frameworks (e.G., CFIR, TDF, RE-AIM) to inform study design, analysis, and interpretation.- Support pragmatic and real-world research intended to inform adoption, scale-up, and sustainability of healthcare interventions.- Translate implementation science concepts into actionable insights for clients.Business Development Support- Contribute to proposal development through methodological input, study design, and drafting of scientific sections.- Participate in client meetings and presentations as a scientific subject matter expert.- Support development of reusable methods, templates, and best practices that enhance proposal quality and efficiency.External Thought Leadership- Contribute to external visibility through conference abstracts, posters, presentations, and peer-reviewed publications.- Represent IQVIA as a credible scientific expert in mixed methods and implementation science under guidance of senior leadership.- Participate in industry working groups, advisory boards, or collaborative initiatives as appropriate.Internal Capability Building & Mentorship- Mentor junior and mid-level staff on study design, analysis, and scientific writing.- Support internal training initiatives, methods development, and communities of practice.- Contribute to quality review processes and continuous improvement of scientific standards.Qualifications & Experience- Advanced degree (PhD, DrPH, MD, PharmD, MSc, or equivalent) in a relevant scientific discipline strongly preferred.- Demonstrated expertise in mixed-methods research, qualitative methods, and survey-based research.- Applied experience using implementation science frameworks in healthcare or life sciences research.- Strong scientific writing and presentation skills, with experience contributing to client-facing and external materials.- Experience working in a consulting or client-facing research environment preferred.- Ability to independently lead multiple projects as a subject matter expert and collaborate effectively across multidisciplinary teams.#J-18808-Ljbffr

Principal/Sr Principal - Global Custom Integrated ResearchBarcelona, Spain | Full time | HybridWe’re passionate about improving the life sciences ecosystem and making decisions that accelerate innovation for a healthier world. Every day our team develops evidence-based strategies that are used in published research, clinical guidelines, and market access decisions, to improve healthcare at every touchpoint. We design and deliver Commercial Analytics, supported by our world-class proprietary data assets, solve complex client challenges through strategic consulting, and use leading edge market research techniques to support clients brand strategy, planning and measurement. We’re purpose-driven problem solvers, that do what we love to make a greater impact on human health.Integrated ResearchWe focus on understanding the behaviours and attitudes of Health Care Professionals and patients to support international pharmaceutical companies to understand them as people. This is across the whole of the product lifecycle. We explore and measure what Health Care Professionals and patients say and do using different behavioural frameworks to deliver actionable insights and clear answers to our clients’ business questions. We typically use IQVIA data to contextualise our research and collaborate with other IQVIA teams to provide our clients with comprehensive solutions to their business issues.The RoleIn this role, you’ll be a senior lead in the Global Custom Integrated Research team. You will drive the growth of the team across multiple different areas, and be a leadership role model to the other seniors in the group.You’ll work directly with multiple clients to develop business opportunities and provide valuable input to solutions, take pride in your work and relationships, and exceed targets. You will also have a strong focus on developing future talent in the team and ensuring the next generation of leaders has clear guidance and growth pathways. The role requires you to develop your own clients and have a high degree of collaboration with other teams, particularly Advisory Services. You will bring innovation to client solutions through the application of new and agile ways of collecting insights and the application of technology, such as AI.What You’ll Be Doing- Proactively bringing solutions to ensure the business is well functioning and the teams have what they need to deliver- Owning significantly sized accounts and meeting or exceeding revenue targets by developing and delivering insightful, value-added solutions that address complex issues- Supporting the evolution of what the team does and how we talk about it to ensure the offering is always compelling to clients- Seeking out and identifying new revenue opportunities and ensuring a continuous flow of business from clients- Applying consultative problem-solving skills to be an Integrated Solutions expert (based on a foundation of market research)- Bringing market research expertise and gravitas to support revenue generation and delivery across other teams, particularly Advisory and Consulting- Developing new, tangible and commercial offerings- Bringing solutions to growth barriers in the business and taking responsibility for their implementation- Contributing to the awareness of IQVIA Custom Integrated Research in the marketplace through speaking engagements, client meetings, and publications- Mentoring, coaching, and sharing expertiseWho You Are- A degree holder with 10/15+ years’ experience in life sciences or healthcare consulting- Expertise in primary market research methodologies and delivery processes- Proven seller of complex engagements to the top Pharma/Life Sciences companies- An established leader, typically of multiple or significantly sized teams, with a record of management and people development- An expert in the identified teams’ solutions, that can produce new and creative ideas- A successful mentor, talent retainer and confident leader that can enable creativity in othersVisit our benefits page for information on everything from perks to well-being initiatives and career enhancement.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.ComIQVIA 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.We champion leadership that drives progress. Recognition in the HBA Awards celebrates our commitment to advancing women in healthcare.#J-18808-Ljbffr

Clinical Research AssociateIQVIA 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 representativesQualifications:- 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 BWhat 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 packageIQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at 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

The team & the companyIQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources and extensive domain expertise.With direct access to the world’s most comprehensive healthcare information, analytics and research resources, IQVIA experts design and deliver innovative data– and technology-enabled evidence programs to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. IQVIA Global Health Economics is a fast-growing and highly successful consultancy business, focusing upon on delivering tangible business results to our clients who are key decision-makers and business managers across the international pharmaceutical and healthcare industry.The IQVIA Global Health Economics team is composed of around 200 highly qualified multi-disciplinary professionals from a variety of disciplines including health economics, health technology assessment (HTA) strategy and evidence generation, based in 12 geographies, with projects delivered across > 50 countries.Our clientsoperate in the life sciences industry, including global top 20 pharmaceutical companies and biotech companies, as well as public health providers and regulatory authorities. They are looking for insight and evidence around the safety, efficacy, effectiveness and cost-effectiveness of health care delivery systems and pharmaceutical products spanning the full spectrum of therapeutic and disease areas. Our diverse mix of clients, the breadth of disease areas, as well as increasing access to novel data sources and methodologies provide a constant and rewarding challenge for our people.For more information about our company please visit our website: https://www.Iqvia.Com/Role purposeThis role will offer you the opportunity to support our Global Health Economics team as a Consultant Medical Writer and be part of our HTA Evidence & Strategy Centre of Excellence and Value Communications Centre of Excellence.This role focusses on medical writing for health economic and outcome research (HEOR) and HTA purposes, where you will be responsible for writing tasks within projects and work with a senior team to co-manage small workstreams, project tasks and thought leadership initiatives.Typical projects include medical writing for EU Joint Clinical Assessment (JCA) dossiers, HTA dossiers (predominantly NICE, SMC, NCPE), global value dossiers (GVDs), payer objection handlers, payer value stories/messaging, literature review protocols and reports, reports for evidence synthesis and health economic modelling studies, and HEOR-focused peer-review manuscripts and conference abstracts. The audience for the project deliverables will be various life-sciences customers as well as healthcare payers, providers, and regulators. You will work within a team of highly experienced health economists and outcomes research specialists providing support across a range of HEOR projects, working in a cross-functional and cross-country project team, providing medical writing, undertaking quality control, and contributing to the management of project delivery (including guiding and reviewing the work of more junior team members).The role will expose the candidate to the broad range of payer-focused offerings in value communications, HTA strategy and HEOR to support in business development opportunities. An ideal candidate will have a good understanding of the matrix structure typical of our clients in the pharmaceutical industry and how to successfully navigate this structure to achieve clients’ aims. Furthermore, the candidate should demonstrate an ability to interpret clinical, economic and real-world evidence and translate findings into compelling value narratives and payer focused communication strategies to optimize a product’s access to markets and its reimbursement.Qualifications and SkillsExtensive experience with medical writing in HEOR/HTA/payer materials is essential for the role. We are looking for proactive individuals with strong analytical and problem-solving skills. Candidates should have a strategic mindset, the ability to identify potential issues and suggest solutions. The ideal applicant should have strong interpersonal skills and the ability to establish relationships with both internal team members and clients. As such, fluency in conversational and business English and strong communication skills is essential. The ability to demonstrate clear scientific communication in English through slide deck development, report writing, and presentations is essential.We recruit individuals from a variety of backgrounds to join our well-rounded team. If you are motivated, have a passion for healthcare, have strong organisational skills, and expertise in payer-focused medical writing we encourage you to apply. Key skills for this role include:- Degree in life sciences (or related), epidemiology or health economics and policy, preferably a Master’s degree; - Significant experiencein medical writing across multiple therapeutic areas (~5 years, minimum 3 years HEOR/HTA experience specifically), including direct experience writing GVDs and/or benchmark HTA submissions (e.G., NICE or G-BA dossiers), peer-reviewed publications, and HEOR study reports/protocols; - Experience managing and coordinating delivery of GVDs and/or benchmark HTA submissions, or parts of these deliverables; - Familiarity with health economics and health technology assessment processes, ideally JCA, NICE or G-BA; - Strong written and verbal English communication skills, expertise in scientific writing requirements; - Ability to produce high-quality written content with minimal guidance from senior team lead; - Excellent Microsoft office skills (expert in use of MS Word), and high attention to detail; - Self-motivated with a strong desire to learn quickly and independently, ability to work autonomously with appropriate guidance when needed; - Strong time-managementand organisational skills, and flexibility to work in a fast-paced environment.Responsibilities- Independently produce high-quality written content for GVDs/HTA dossiers (JCA, NICE, and/or G-BA), HEOR study reports (e.G., SLR, NMA, ITC, modelling, secondary database research, manuscripts, conference abstracts, and other payer materials (e.G., objection handler, value story / value proposition development) with minimal guidance from project manager; - Ability to collaborateeffectively across multidisciplinary and geographically dispersed teams; - Work with senior team to co-manage small projects or workstreams, project tasks and thought leadership initiatives (i.E., guide junior team members, first review junior team members output, client management); - Conduct quality control reviews of HEOR documents and maintaining audit trails of changes; - Mentor and train less experienced Medical Writers; - Contribute to medical writing training initiatives to upskill the team and set quality standards; - Support the team’s Centre of Excellence initiatives; - Manage your own time and responsibilities to meet project requirements with clear communication with project managers, line manager and resource manager to ensure utilisation and compliance targets are met.Important- Please note that we don't provide any visa suport.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

IQVIA Argentina is seeking a Principal/Sr Principal for its Global Custom Integrated Research team in Barcelona. This leadership role requires expertise in market research and a strong background in the life sciences, aimed at driving innovation and growth.The ideal candidate will have over 10 years of experience, a successful track record of client engagement, and the ability to mentor the next generation of leaders. The position offers a hybrid working model and opportunities for professional development.#J-18808-Ljbffr

ALTEN Spain busca un/a Change/Project Manager para liderar la gestión del cambio en implementaciones P2P y apoyar la integración de Coupa P2P en Colombia, México y Argentina.

Si cree que es el candidato ideal para la siguiente oportunidad, envíe su solicitud después de leer la descripción completa.IQVIA is a fast-growing and highly successful consultancy business, focusing on delivering tangible business results to our clients who are key decision-makers and business

IQVIA is seeking an HTA Analyst to support UK HTA submissions and engagement with agencies such as NICE and the SMC.Si está considerando enviar una solicitud, asegúrese de pulsar el botón de solicitar de abajo después de leer la descripción completa.The role offers flexibility for office and ho

IQVIA is seeking a Clinical Biospecimen Scientist for a Single Sponsor Dedicated program based in Barcelona.Todo listo para enviar su solicitud? Asegúrese de comprender todas las responsabilidades y tareas asociadas a este puesto antes de continuar.This full-time, home-based role focuses on managin

IQVIA is seeking a Sales Executive, Life Sciences, Safety Technology, in the EMEA region to drive growth across the pharmacovigilance portfolio.Está considerando presentar su candidatura para este trabajo? Compruebe todos los detalles en esta descripción del puesto y luego haga clic en "Solicitar"

IQVIA is seeking a Senior Business Analyst to join our remote Connected Devices Product Delivery team.La descripción completa del puesto cubre todas las habilidades asociadas, la experiencia previa y cualquier cualificación que se espera que tengan los solicitantes.You will lead gathering, analyzi

Clinical Independent Rater - Romanian Speaking.La siguiente información tiene como objetivo proporcionar a los posibles candidatos una mejor comprensión de los requisitos para este puesto.Hours: Estimated 10–16 hours per month.Role: Clinical Independent Rater for Clinical Trials.IQVIA is a globa

IQVIA seeks a Director of Global Business Development – Brand Outsourcing and HCP Engagement to drive growth across international markets.Consulte la descripción del puesto a continuación.Si confía en que tiene las habilidades y la experiencia adecuadas, envíe su solicitud hoy mismo.The role i

Associate Principal - Mixed Methods Research: Patient Experience - Home-based/Hybrid.Es usted el solicitante adecuado para esta oportunidad? Descúbralo leyendo el resumen del puesto a continuación.Barcelona, Spain | Full time | Hybrid | R1536610.Associate Principal, Implementation Science & Mixed

IQVIA is a leading global provider of clinical research services, safety publishing, and healthcare intelligence.Está considerando presentar su candidatura para este trabajo? Compruebe todos los detalles en esta descripción del puesto y luego haga clic en "Solicitar".This role focuses on reviewing

IQVIA Spain is seeking a Clinical Research Associate (junior CRA) to join our Sponsor dedicated team.Por favor, verifique que tiene el nivel de experiencia y las cualificaciones adecuadas leyendo la descripción completa de esta oportunidad a continuación.You will gain experience across therapeutic

IQVIA Argentina is looking for a Senior Clinical Research Associate to be based in Barcelona, Spain.

Le gusta esta oportunidad? Asegúrese de inscribirse rápido, ya que se espera un gran volumen de solicitudes.Desplácese hacia abajo para leer la descripción completa del puesto.Sponsor dedicated team as junior CRA.At this position you will have the opportunity to put your passions to work in an e

Acts as Lead Medical Writer on most types of writing projects.Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the agreed timelines.Performs Senior Review of straightforward medical writing deliverables.Negotiates timel

IQVIA in the UK and across Europe seeks an Associate Director to lead HTA strategy and implementation, driving market access and value communication for pharmaceutical clients.Obtenga más información sobre las tareas generales relacionadas con esta oportunidad a continuación, así como sobre las

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry.We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world.IQ

IQVIA seeks a Medical Information Specialist with Italian or Spanish, English, and another language to handle medical inquiries and safety data across multiple therapeutic areas.Obtenga más información sobre este puesto leyendo los detalles a continuación y luego envíe su solicitud para ser cons

IQVIA is seeking a Lifecycle Safety Information Specialist to support healthcare professionals and consumers with adverse events, product quality inquiries, and medical information requests.Es usted el solicitante adecuado para esta oportunidad? Descúbralo leyendo el resumen del puesto a continuaci

IQVIA is seeking a Consultant Medical Writer to join the Global Health Economics team.La siguiente información tiene como objetivo proporcionar a los posibles candidatos una mejor comprensión de los requisitos para este puesto.You will create HEOR and HTA medical writing deliverables and work with

This job is available in the UK and in EU countries.Don't hesitate to apply if you're interested either in the UK or in any EU country, even if not all of them are listed.Recuerde revisar su CV antes de enviar la solicitud.Además, asegúrese de leer todos los requisitos relacionados con este puesto

IQVIA is seeking a Director/Senior Director of Business Development for Clinical Solutions across the EMEA region.Maximice sus posibilidades de que su candidatura sea seleccionada asegurándose de que su CV y sus habilidades se ajustan al perfil.This leadership role drives strategic growth with phar

Se pueden requerir diversas habilidades interpersonales y experiencia para el siguiente puesto.Por favor, asegúrese de consultar la descripción a continuación con atención.Collaborate with pre and post award stakeholders to manage the coordination, planning, quality and implementation of Patient

Join us on our exciting journey!.Es esencial asegurarse de que cumple con los requisitos como solicitante para este puesto; por favor, lea atentamente la información a continuación.Director/Senior Director, Business Development – Clinical Solutions, EMEA.IQVIA™ is The Human Data Science Compan

Join us on our exciting journey!.Para una comprensión completa de esta oportunidad y de lo que se requerirá para ser un candidato exitoso, siga leyendo.IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patien

A continuación se detalla todo lo que necesita saber sobre lo que implica esta oportunidad, así como lo que se espera de los solicitantes.Apply knowledge and expertise including complex decision-making activities to review, assess and process Safety data and information across service lines.Recogn

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry.We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world.Lear

Le interesa este puesto? Puede encontrar toda la información relevante en la descripción a continuación.IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry.IQVIA creates intelligent connections across all asp

IQVIA Argentina is looking for an Associate Principal to drive mixed-methods research and implementation science.

IQVIA is seeking a Clinical Independent Rater who is fluent in Romanian to work remotely on a part-time basis.Es usted el solicitante adecuado para esta oportunidad? Descúbralo leyendo el resumen del puesto a continuación.The role focuses on reviewing clinical scales, ensuring assessment quality,

Somos una pareja joven de 40 aos.Catalina (Argentina) y Pau (catalan) :).Se llama Teo es hermoso inquieto y muy simptico.Queremos empezar a recuperar nuestro espacio como pareja.Y buscamos ayuda puntual para salir a cenar los fines de semana , viernes o sbado por la noche.O algn otro da puntual que

Use your scientific and foreign language expertise to join the world’s leading comprehensive pharmaceutical safety services organization at on a fast-growing team performing medical information call center services.Apply your knowledge and expertise, including complex decision making, to review, a

IQVIA busca Delegado/a Especialista en medicina estética para desarrollar presencia de productos en Barcelona, gestionando un territorio y estableciendo relaciones con médicos estéticos.

L’Obrador en Barcelona busca un Oficial de 2ª de panadería para trabajar en Av.La experiencia que se espera de los solicitantes, así como las habilidades y cualificaciones adicionales necesarias para este trabajo, se enumeran a continuación.República Argentina, 177, Sarrià-Sant Gervasi.Reali