Redacción y Edición jobs in Barri De Les CortsCreate job alerts

Buscamos una persona freelance capaz de gestionar postproduccion/edición de proyectos de inicio a fin en Davinci Resolve.Preparación de proyectos, edición, FX, color grading,.Que tenga capacidad analítica, que sea un poco autodidacta y organizada.Se valorará positivamente una carta de motivaci�

This shift-based role is ideal for early-career editors with an interest in digital news, business, and markets. Dow Jones is seeking a digitally minded Platform Editor to join the NewsPlus team, a real-time news portal for financial professionals.

Necesito un servicio de Traductor jurado con las siguientes características:ul br/li¿qué tipo de servicio necesitas? /li Traducción jurada br/li¿en qué idioma está el documento original a traducir? /li Alemán br/li¿a qué idioma hay que traducir el documento original? /li Español br/liIndi

This role focuses on crafting engaging copy for social and digital campaigns, transforming product claims into compelling narratives.

D&M asesores consultores busca incorporar un perfil financiero para dar soporte en consolidación y reporting del grupo.

You will prepare financial statements, close monthly books, and manage AR/AP, ensuring compliance and accurate tax reporting.

Description A Translation Specialist has exceptional linguistic and translation skills, organization and attention to detail, and excellent communication to manage relationships with colleagues, external partners and other stakeholders.The Translation Specialist manages quality by assessing and scor

Multiplica Talent busca un Contable Senior para asegurar la integridad de la información financiera y contable en España, garantizando cumplimiento legal, fiscal y de normas internas. Se requiere experiencia en ciclo contable, gestión de nómina y cumplimiento fiscal.

REMEDY EDGE™ SPAIN is looking for a Senior Medical Editor to ensure the highest quality across medical content, leading editorial excellence and fostering collaboration within a skilled team.

Kymos Group is expanding its international finance team with a new role focused on Compliance & Reporting. Responsibilities include group financial reporting, tax compliance, audits, budgeting and exposure to European funding programs.

Empresa del sector editorial necesita incorporar a su equipo, un/a Editor/a Funciones: •Diseñar nuevos proyectos de edición de libros de texto de ciencias. Coordinar y supervisar el proceso de edición de los libros en todas sus fases cumpliendo con los calendarios y nivel de calidad establecid

FUTURE TRACK en Barcelona busca un profesional de contabilidad para gestionar de forma integral el ciclo contable de varias sociedades, garantizando la fiabilidad de la información financiera y el control analítico por centros de coste. Entre las funciones destacan cierres contables trimestrales,

Responsibilities Start as an Editorial Trainee working in close collaboration with Managing Editors, learning the end‑to‑end process of handling papers from submission to publication. You will execute editorial work for journals in your domain of expertise, organize the review process for manusc

Impress, Europe’s leading Health-Tech innovator, is seeking a Copywriter & CRM Content Specialist to craft CRM content across emails, SMS, push, and in‑app messages.

Grupo Planeta busca un/a Administrativo/a Comercial en Barcelona para dar soporte a la división editorial.

Dow Jones & Company, Inc. is looking for a Manager, Automation & Reporting in Barcelona to lead a global team focused on data insights and robust reporting capabilities. The role involves overseeing the development of reporting solutions, mentoring technical analysts, and ensuring data accuracy using SQL and Python. The ideal candidate will have 5+ years of experience in data analytics, a strong background in cloud data warehousing, and proven expertise in business intelligence platforms. #J-18808-Ljbffr

pAllianz Technology in Barcelona is looking for a Controlling Reporting Specialist to manage financial indicators and improve controlling processes. You will advise managers and ensure compliance with standards while handling reporting and analysis. /ppThe ideal candidate should have experience in controlling, analytical thinking, and a relevant degree. The position offers a hybrid work model, flexible working options, and a comprehensive benefits package. /p #J-18808-Ljbffr

An international commodities firm in Barcelona is seeking a Middle Office Intern to support Value Chain Leads with reports and data analysis. The ideal candidate will be pursuing studies in Finance or Accounting, with strong data management skills. Responsibilities include preparing risk position reports in SAP, reconciling data across countries, and ensuring compliance with controls. Proficiency in English is essential, with additional European languages seen as advantageous. This internship offers hands-on experience in a dynamic work environment.#J-18808-Ljbffr

ph3Discovery and Translational Science Data Science Consultant – Barcelona, Spain /h3 pWe are looking for a bDiscovery and Translational Science Data Science Consultant /b to join a dynamic team of bioinformatics and data scientist consultants in bBarcelona /b, Spain, within Clarivate bLife Sciences Healthcare (LSH) /b, reporting to the Discovery and Translational Science Consulting Manager. /p pThis is a unique opportunity to work across our LSH portfolio and to support innovation in biomedical research by providing bioinformatics and data science services to clients ranging from major pharmaceutical companies to biotech start-ups. We have a great skill set in applying a wide range of computational and systems biology tools to understanding of human disease and the development of novel therapies. /p pWe would love to speak with you if you have experience in doing the same! /p h3About You – Experience, Education, Skills, And Accomplishments /h3 ul liAt least 5 years of hands‑on experience in Data Science /li liPh.D. or M.Sc. in Data Science, Computational Biology, Bioinformatics, AI/ML, or related field /li liProven experience in applying advanced analytics, Machine Learning, and AI to solve complex problems in Life Sciences. /li liStrong proficiency in Python and/or R /li liExperience with machine learning frameworks (e.g., PyTorch, TensorFlow), NLP libraries (Hugging Face Transformers, spaCy), knowledge graphs (Neo4J, Amazon Neptune) and biomedical ontologies. /li /ul h3It Would Be Great If You Also /h3 ul liExperience with multi‑modal AI (combining -OMICs, imaging, and text). /li liFamiliar with cloud computing and workflow orchestration tools. /li liUnderstand Life Sciences concepts (genomics, proteomics, clinical data). /li liApplied your skills in the context of human disease and drug discovery research /li liExperience with large‑scale omics datasets and data integration. /li liExposure to knowledge graphs and RAG systems /li /ul h3What Will You Be Doing in This Role? /h3 ul liAnalyze large‑scale biological, clinical, and multi‑omics datasets to extract biological insights /li liDevelop predictive models for disease progression, drug response, and patient stratification. /li liDesign scalable, reproducible workflows for data processing and model deployment using Python, R, and cloud platforms. /li liIntegrate structured and unstructured data sources for multi‑modal analysis. /li liBuild NLP pipelines for entity recognition, ontology mapping, literature mining, and hypothesis generation. /li liConstruct, expand and analyze knowledge graphs using graph representation learning techniques (e.g., GNNs, matrix factorization). /li liCreate interactive visualizations and reports to share your findings with clients and teammates. /li liProvide technical leadership: mentor teammates, guide best practices, and drive innovation across projects. /li /ul h3About The Team /h3 ul liWe are a growing team of more than 25 consultants mostly based in Barcelona, Spain with some team members based throughout the rest of Spain and US. /li liWe provide a wide range of bioinformatics services supporting clients from big pharma to small biotech start‑ups, often leveraging Clarivate’s unique content in drug discovery and translation. /li liOur work is mostly focused on understanding of disease mechanisms, identification of novel targets and translational medicine support through discovery of biomarkers and patient stratification. /li liWe also run two consortia with major industry partners around implementation and benchmarking of bioinformatics and Systems Biology algorithms. /li liThe team culture is dynamic with focus on collaboration and mutual support. /li /ul h3Hours of Work /h3 ul liThis is a permanent full‑time position at 40 hours a week (35 hours during July and August). /li liThe position is hybrid going to the office in Barcelona 2-3 times per week. /li liThe working schedule is flexible, mostly centered on CET time zone with occasional need to accommodate late or early meetings with US or East Asia time zones. /li /ul h3What We Can Offer You /h3 ul liVolunteering community offering paid hours of volunteering time /li liPrivate Health and Life Disability insurances. /li liTax‑free benefits (Ticket Restaurant scheme, kindergarten and transport cards). /li liLanguage classes (Catalan, Spanish and English). /li liGlobal and dynamic employee base (more than 40 nationalities). /li li30 working days of vacation. /li /ul pAt Clarivate, we are committed to providing equal employment opportunities for all qualified persons with respect to hiring, compensation, promotion, training, and other terms, conditions, and privileges of employment. We comply with applicable laws and regulations governing non‑discrimination in all locations. /p /p #J-18808-Ljbffr

Estamos en la búsqueda de un experimentado.El candidato ideal será responsable de la supervisión y optimización de los servicios de Analítica y Reporting, trabajando en estrecha colaboración con un equipo de servicio externalizado encargado de la administración de las plataformas tecnológica

Experteer Overview In this role, you enable data-driven HR decisions by delivering advanced Workday reports and dashboards that support global HR operations. You will partner across HR, Finance, and IT to standardize reporting and governance while ensuring data privacy and regulatory compliance. The position sits in the Global HR Digital Team, driving HR transformation through digital solutions and insights. You will influence strategic decisions by turning data into actionable analytics, across 30+ countries. Compensaciones / Beneficios • Design and deliver advanced Workday reports and dashboards (Advanced, Matrix, Composite, Trending) • Develop complex calculated fields and reporting logic using Workday data sources • Own and evolve global HR reporting governance, including report inventory, standards, certification, and access controls • Ensure reporting solutions meet data privacy, security, and regulatory requirements (e.g., pay transparency) • Translate business requirements into scalable analytics solutions with HR, Finance, and COEs • Enable self-service reporting through standardized dashboards, discovery boards, and training • Maintain audit-ready documentation for critical reports and processes • Continuously optimize reporting solutions to reduce manual effort and improve data accessibility Responsabilidades • 5+ years of hands-on Workday reporting experience with Advanced, Matrix, Composite, and Trending reports • Advanced proficiency in calculated fields, business objects, and Workday data architecture • Strong understanding of Workday security model and data access controls • Proven ability to design scalable reporting solutions aligned to global HR data standards • Experience supporting regulatory and compliance reporting (e.g., pay equity, workforce disclosures) • Strong analytical and problem-solving skills with ability to translate data into insights • Experience in global, matrixed environments with cross-functional stakeholders • Familiarity with Workday Prism, Discovery Boards, or external BI tools (Power BI/Tableau) is a plus Requisitos principales • remote work option

Darwin Recruitment is seeking a PMO Analyst to support project portfolio governance and reporting. The successful candidate will leverage AI and modern tools to improve reporting and increase productivity. ¿Quiere presentar una candidatura? Asegúrese de que su CV está actualizado y luego lea atentamente las siguientes especificaciones del puesto antes de solicitar. This role is based in Barcelona, Spain, offering flexibility for remote work. Responsibilities include maintaining the portfolio log and ensuring compliance with PMO standards. xcskxlj Competitive rate for a contract length of 5 months with an ASAP start date. Interested candidates should apply with an updated CV. #J-18808-Ljbffr

Bluespace, empresa líder en Self Storage en España, busca dos Learning Content Creators para desarrollar vídeos y recursos formativos para aprendizaje online de los empleados.

pNews Corporation is searching for a Manager for the Automation Reporting team to lead skilled analysts in data insights. The role involves overseeing the development of reporting solutions, managing projects, and mentoring team members. Candidates should have over 5 years of experience with SQL and Python, along with a solid background in data analytics. /ppThis position is based in Barcelona and offers comprehensive insurance plans and employee benefits. /p #J-18808-Ljbffr

Grupo Digital, ubicado en Barcelona, busca un profesional en SAP BI para desarrollar y mantener reportes avanzados. El rol implica un fuerte enfoque en la validación y mejora de soluciones SAP BusinessObjects.Se requiere experiencia en el análisis de datos, resolución de incidencias y soporte a usuarios, además del manejo de herramientas de datos como SAP BW y Oracle.La posición es presencial y ofrece una jornada completa y un salario según la experiencia entre 30.000 y 35.000 € brutos anuales.#J-18808-Ljbffr

Bunge is seeking a proactive Data Analyst to manage and evolve reporting pipelines, analytics, and automation across its European digital transformation unit for sales and marketing programs. You will design, build, and maintain end-to-end data pipelines to ensure high-quality, standardized reporting. Strong collaboration with data engineers and analysts is essential, along with advancing AI-powered insights and narratives. #J-18808-Ljbffr

As part of one of the world’s most admired healthcare advertising agencies, Remedy Edge Spain brings people, brands, ideas and innovation together to change real lives in extraordinary ways. ¿Listo para inscribirse? Antes de hacerlo, asegúrese de leer todos los detalles pertenecientes a este trabajo en la descripción a continuación. Our core values allow us to work with clients in a way that changes their perception of what an agency can and should be. We lift each other up, challenge each other, demand from each other and encourage each other because we are responsible for each other. We work tirelessly to protect what we’ve built because it allows us to be who we are: dreamers, builders, pioneers, friends, lifechangers. We belong to Omnicom Health Group, the largest healthcare marketing and communications network in the world, with more than a dozen companies and over 4,000 talented people specializing in every area of health. Our people come from every corner of science, medicine, marketing, and communications, partnering with clients—and connecting with each other— to achieve meaningful change through better, more innovative communications. About the role The Medical Writer Supervisor’s work focuses on developing and supervising scientific content (from slide decks to monographs, promotional materials, abstracts, article reviews, congress reports and more). Key Responsibilities • Supervision of medical and publication strategies., • Devising medical and publication strategy, • Bibliographic background research, • Creation, editing, and validation of scientific materials, • Ensuring proper referencing and scientific accuracy of all materials. Incorporating all feedback provided by the client in a proper and timely manner, • KOL management Skills & Experience • Must have a health science degree (e.g. in biology, pharmacy or medicine). PhD is a plus, • 5 years of experience in medical writing and scientific content supervision., • Ability to communicate medical/technical information to a wide variety of audiences, • Key Opinion Leaders management, • Ability to work in a deadline-driven environment, • Attention to detail and absolute reliability in meeting delivery deadlines, • Native/Bilingual Spanish or English speaker, • Team player who can foster positive relationships between the department and other agency teams, such as creatives and account managers, • Experience with reference managers such as EndNote is a plus Our Commitment Omnicom Health Group is committed to hiring and developing exceptional talent. xcskxlj We agree that talent is equally distributed, and we’re focused on developing diverse teams that can bring the best solutions to everything we do. We strongly believe that celebrating what makes us different makes us better together. Join us—we look forward to getting to know you. #J-18808-Ljbffr

pp¿Cuál es tu disponibilidad de incorporación? /p pPreaviso de 15 días /p p¿Cuáles son tus expectativas salariales bruto/año? /p h3Información personal /h3 pNombre /p pApellidos /p pTeléfono /p pEmail /p pURL personal /p h3Información sobre la solicitud /h3 pCarta de presentación /p pCurriculum vitae /p pSubir archivo (máx. 10MB) /p pImagen de perfil /p pSubir archivo (máx. 10MB) /p h3Preguntas /h3 p¿Cuál es tu disponibilidad de incorporación? /p pTotal e inmediata /p pPreaviso de 15 días /p pOtro /p p¿Cuáles son tus expectativas salariales bruto/año? * /p pEntre 25.000 - 30.000 brutos/año /p pEntre 30.000 - 35.000 brutos/año /p pEntre 35.000 - 40.000 brutos/año /p pSuperiores a 45.000 brutos/año /p pHe leído y acepto la Política de privacidad /p pSí, BME SPAIN puede añadirme a la bolsa de talentos y ponerse en contacto conmigo cuando haya futuras oportunidades de empleo. /p pRevisa la información básica sobre protección de datos /p pEVERYDAY SOFTWARE, S.L. tratará tus datos personales con el fin de gestionar tu candidatura en el proceso de selección. La base legal para este tratamiento es la ejecución de medidas precontractuales solicitadas por ti en relación con una posible relación laboral. Además, Factorial puede utilizar una herramienta de IA llamada “Match” para ayudar al reclutador en la decisión final de contratación. Esta herramienta no toma decisiones por sí misma. El tratamiento de los datos se basa en el interés legítimo de identificar a los candidatos con mayor potencial para el empleo. Para más información, puedes consultar la Política de Candidatos. /p pTen en cuenta que puedes ejercer tus derechos conforme a la ley de protección de datos en cualquier momento, contactándonos en /p /p #J-18808-Ljbffr

ppTransPerfect Is More Than Just a Jobu2026 /p pOur greatest asset is our people, and nothing is more important to us than ensuring that everyone knows that. Each of our 100+ offices has its own individual identity, and each also has its own unique rewards. /p h3Position Summary /h3 pThe Translation Project Coordinator plays a key role in coordinating multilingual projects from start to finish. They collaborate with internal teams and global vendors to ensure projects are delivered on time, within budget, and to the highest quality standards. This is a fast-paced, detail-oriented role ideal for someone who thrives on organization, problem-solving, and cross-cultural communication that is keen to enter the industry in a hands‑on, entry-level role with unlimited learning and growth opportunities in the industryu00b4s leading company. /p h3Position Responsibilities /h3 ul liCoordinate the full lifecycle of multiple localization and translation projects simultaneously /li liCoordinate all project phases, from initiation to delivery, ensuring smooth execution /li liCollaborate with Sales/Client Services teams to define project scope, timelines, and requirements /li liCommunicate with our global network of vendors (translators, editors, and other specialists) to negotiate rates, assign tasks and agree on deadlines, and subsequently monitor project progress /li liTrack project status, proactively identifying and resolving issues with involved stakeholders /li liManage project budgets, including cost tracking, gross margins and financial reporting /li liMaintain accurate and organized project documentation /li liPerform quality control checks at various stages (e.g. proofreading, final-eye reviews of deliverables, etc.) /li liEnsure compliance with internal processes and quality standards /li liComplete all other tasks that are deemed appropriate for this role and assigned by the manager/supervisor. /li /ul h3Essential Skills Required /h3 ul liBacheloru00b4s degree or equivalent /li liSuperior written and spoken communication skills in English /li liMinimum 1 year of professional experience in a similar position in corporate environment /li liAbility to work both independently and take initiative, while also being comfortable collaborating effectively with multiple internal and external stakeholders on an international level /li liStrong organizational skills with the ability to multitask and prioritize effectively /liliHigh attention to detail and commitment to quality /li liGood analytical and problem-solving skills /li liProficiency in MS Office and general computer skills /li /ul h3Desired Skills And Experience /h3 ul liKnowledge of additional languages at professional working proficiency /li liExperience in translation/localization project management /li liFamiliarity with CAT tools or localization platforms /li /ul pTransPerfect provides equal employment opportunities to all individuals regardless of their race, color, creed, religion, gender, age, sexual orientation, national origin, disability, veteran status, or any other characteristic protected by local law. /p pWe celebrate diversity as one of our core values and we have a clear goal: to be an inclusive workplace where a diverse mix of talented people want to come, stay and do their best work. Together with passionate, creative and collaborative colleagues, we are working to ensure accessibility is for everyone. /p pBy applying, I confirm I have read and accept TransPerfect's Privacy Policy: /p /p #J-18808-Ljbffr

pRemedy Edge Spain is seeking a Medical Writer Supervisor to lead the development and supervision of scientific content, from slide decks to monographs and abstracts. You will oversee medical and publication strategies and ensure scientific accuracy while coordinating with clients and cross-functional teams. /ppIdeal candidates have 5 years of medical writing experience, a health science degree, and the ability to convey complex medical information to diverse audiences. /p #J-18808-Ljbffr

pGrupo Ferrer Internacional busca un profesional para apoyar procesos ESG y la recopilación de información para informes y estándares (EINF, CDP, EcoVadis, CSRD). Participarás en la implementación de herramientas de reporting y en la gestión ambiental y social de la cadena de valor. /ppSe valoran formación en sostenibilidad, dominio de Excel y Power BI, y habilidades de comunicación para formación y campañas. Se ofrece un modelo de trabajo híbrido y oportunidades de desarrollo. /p #J-18808-Ljbffr

ph3ExtraDixital /h3pLa productora audiovisual Indaloy Media prepara un nuevo formato televisivo y abre proceso de selección para incorporar perfiles de redacción. La posición está orientada a profesionales con buena capacidad de escritura y sensibilidad para trabajar contenidos dirigidos a un público adulto. /ph3Funciones /h3ulliBúsqueda de perfiles para participación en el programa /liliRedacción de informes y fichas de contenido /liliSeguimiento y coordinación de invitados /li /ulh3Perfil /h3ulliFormación en Periodismo o Comunicación /liliExperiencia previa en funciones similares (valorable) /liliExcelente capacidad de redacción /liliCapacidad de trabajo en equipo /liliEmpatía con público objetivo mayor de 50 años /li /ul /p #J-18808-Ljbffr

Syneos Health is seeking a Medical Writer in Barcelona, Spain. The role involves compiling, writing, and editing clinical and regulatory documents, ensuring high-quality completion of projects. Responsibilities include adhering to regulatory guidelines, coordinating reviews, and maintaining client relationships. The candidate should be proactive in seeking solutions and managing project budgets. This role may require minimal travel (less than 25%) and aims to enhance professional development in line with industry standards.br#J-18808-Ljbffr

We’re hiring: ESG Reporting Specialist! Lea atentamente toda la información sobre esta oportunidad y luego utilice el botón de solicitud de abajo para enviar su CV y su candidatura. Do you want to make a real impact and help shape the future of sustainability in a global company? This is your opportunity. At Roca Group, we are strengthening our Sustainability team and looking for a passionate and detail‑oriented ESG Reporting Specialist to elevate our non‑financial reporting and drive continuous improvement across our ESG performance. What you'll do • Coordinate ESG data collection across teams and geographies, • Ensure high‑quality, consistent, and traceable sustainability information, • Support our Sustainability Report and other non‑financial disclosures, • Work with leading frameworks: ESRS, CSRD, GRI, TCFD, EU Taxonomy, • Manage ESG questionnaires, client requests, and external ratings (incl. EcoVadis), • Collaborate on double materiality, dashboards, LCA/EPD projects, and ESG risk analysis, • Identify opportunities to digitalize and automate reporting processes What we're looking for • 2-5 years of experience in sustainability reporting or ESG consulting, • Strong analytical mindset and attention to detail, • Solid knowledge of ESG standards and regulatory frameworks, • Advanced Excel skills; BI tools are a plus, • High level of English, • Experience with CSRD/ESRS implementation or external assurance is highly valued Why join us? You’ll be part of a collaborative, forward‑thinking team working on meaningful projects that directly contribute to our sustainability strategy and long‑term impact. If you’re ready to grow, innovate, and help us build a more sustainable future, we’d love to meet you. The recruitment process is governed by equal opportunity, without descrimination based on ethnic origin, nationality, gender, marital status, religion, opinion, sexual preference or any kind of physical, personal or social condition. xcskxlj The selection of the candidate will be based on their merits and skills, taking into account the competencies and aptitudes required for the requested profile. #J-18808-Ljbffr

ph3About the Company /h3 pBiorce is a pioneering Healthtech company dedicated to revolutionizing drug development through the power of AI. We are passionate about accelerating medical advancements and improving patient outcomes. /p pOur team comprises seasoned clinical research professionals, data scientists, and AI experts, working collaboratively to bridge the gap between cutting‑edge technology and real‑world clinical needs. /p pWith an unwavering commitment to revolutionize healthcare, we envision a world where all patients benefit from accelerated and cost‑effective access to treatments. Biorce is poised to redefine the landscape of healthcare, shaping a future where innovation and accessibility converge for the betterment of humanity. /p h3About the Role /h3 pFollowing our successful expansion into the U.S. and continued growth across Europe, we are seeking a Medical Writer to help drive our Scientific function from our Austin or Barcelona hubs. /p pReporting directly to our Chief Scientific Officer, this person will play a critical role as the medical voice behind Aika, ensuring that what we build, publish, and communicate is grounded in sound medical science, clinical best practice, and patient‑centric thinking. The focus is on hands‑on scientific writing, publications, and content. /p pbWho We're Looking For: /b /p pA scientifically trained professional with strong writing instincts and a track record in clinical development, medical affairs, medical writing, or scientific communications. We're looking for someone who can hold the medical pen on high‑stakes documents and, at the more senior end, represent Biorce credibly with KOLs, sponsors, and regulators. /p pThis person should be able to combine sharp scientific judgment with clear, compelling writing: producing everything from peer‑reviewed publications to medical input on product workflows. /p h3Key Responsibilities /h3 ul liProduce high‑quality scientific outputs: peer‑reviewed publications, white papers, value dossiers, conference materials, and other written deliverables that strengthen Aika's credibility. /li liContribute to medical and scientific input on Aika's core clinical functionalities, including protocol design support, eligibility logic, and endpoint frameworks. /li liPartner with Product and Commercial teams to ensure AI models and workflows reflect current standards of care, clinical guidelines, and regulatory considerations. /li liTranslate complex clinical and scientific concepts into clear, accurate, and engaging content for different audiences (sponsors, KOLs, internal teams, external publications). /li liAct as a scientific voice for Biorce externally: supporting advisory boards, scientific conferences, and strategic partner discussions. /li liShape the medical and therapeutic direction of the platform, prioritising work that addresses real‑world challenges in drug and device development. /li /ul h3Requirements /h3 ul liAdvanced scientific or clinical background: life sciences, pharmacy, medicine, or related (a medical degree, PharmD, or clinical PhD is required). /li liExperience in clinical development, medical affairs, medical writing, scientific communications, or a related function in pharma or biotech. /li liSolid understanding of clinical trial methodology, endpoint selection, and benefit‑risk assessment. /li liExcellent scientific writing skills with a portfolio of published or client‑facing work. /li liStrong stakeholder management skills and high integrity. /li /ul h3Nice‑to‑Haves /h3 ul liExperience working with or overseeing digital health and AI‑driven platforms. /li liExposure to multiple therapeutic areas or indications. /li liExperience presenting at scientific conferences or sitting on advisory boards. /li liHands‑on experience with protocols, eligibility criteria, endpoints, or regulatory documents. /li /ul h3Why Join Us? /h3 ul liA dynamic work environment with an international team, where collaboration and diversity thrive. /li liWork alongside top talent, united by a shared purpose and committed to making a real impact. /li liComprehensive private health coverage to ensure your physical and mental well‑being. /li liHybrid work model offering flexibility to balance your professional and personal life. /li liCompany events to celebrate achievements and enjoy time together. /li liGet equipped with a MacBook to enhance your productivity and work experience. /li liOur office is pet‑friendly! You'll likely be greeted by a few wagging tails upon arrival. /li /ul /p #J-18808-Ljbffr

Catenon busca un Financial Controller para integrarse en una empresa de capital privado dedicada a la distribución de productos de tabaco y bebidas alcohólicas, con presencia internacional. Reportando al CFO, serás responsable de dar soporte financiero y de controlling a filiales, profesionalizando procesos y mejorando el reporting para apoyar el crecimiento. Se valorará experiencia en entornos multinacionales y coordinación de operaciones internacionales. #J-18808-Ljbffr

Experteer Overview In this role you drive bioinformatics and data science projects that illuminate disease mechanisms, identify drug targets, and support biomarker discovery. You work within a growing Barcelona team to deliver analyses, guide project scope, and shape new offerings for pharma and biotech clients. Expect hands-on analysis, collaboration with cross-functional teams, and opportunities to impact translational medicine programs at scale. Compensaciones / Beneficios • Apply state-of-the-art bioinformatics tools and the Systems Biology Platform to generate hypotheses on disease mechanisms, drug response biomarkers, and targets • Manage and execute bioinformatics analyses, ensuring adherence to scope, timeline, and budget • Scope client bioinformatics projects by understanding needs and defining analytical strategy • Contribute to portfolio development and improvement of bioinformatics offerings • Collaborate with cross-functional teams and clients to drive project success Responsabilidades • 5 years of relevant experience • Proven experience in Bioinformatics, Computational or Systems Biology or related field • Master’s Degree in Life Sciences with strong computational component or in Computer/Data Science with Life Sciences component • Advanced user of R, Python, and Linux/Unix with strong statistics/data analysis • Experience applying statistical methods, AI/ML to large omics datasets, building predictive models, and generating actionable insights • Experience defining bioinformatics projects and executing them independently • Industry experience or providing bioinformatics as a service Requisitos principales • private health insurance • life & disability insurance • Tax-free benefits (Ticket Restaurant, kindergarten, transport cards) • language classes (Catalan, Spanish, English) • volunteering time • 30 vacation days

Tamarind Intelligence in Barcelona is seeking a talented Midweight Copywriter to join their creative team. This role focuses on crafting engaging copy for social and digital campaigns, transforming product claims into compelling narratives. Ideal candidates will have 3-5 years of agency experience and a strong portfolio that showcases campaign thinking.Join Tamarind Intelligence to work in a vibrant environment that values creativity and cultural relevance, while also enjoying flexible work options and comprehensive wellness benefits.

pImpress, Europe’s leading Health-Tech innovator, is seeking a Copywriter CRM Content Specialist to craft CRM content across emails, SMS, push, and in‑app messages. You’ll translate and localize content for multiple markets, partner with design to optimize visuals, and help deploy campaigns with automation workflows. /ppYou’ll drive engagement by refining customer journeys, monitoring performance, and collaborating with diverse teams to align campaigns with business goals. /p #J-18808-Ljbffr

ph3ExtraDixital /h3pLa productora audiovisual Indaloy Media prepara un nuevo formato televisivo y abre proceso de selección para incorporar perfiles de redacción. La posición está orientada a profesionales con buena capacidad de escritura y sensibilidad para trabajar contenidos dirigidos a un público adulto. /ph3Funciones /h3ulliBúsqueda de perfiles para participación en el programa /liliRedacción de informes y fichas de contenido /liliSeguimiento y coordinación de invitados /li /ulh3Perfil /h3ulliFormación en Periodismo o Comunicación /liliExperiencia previa en funciones similares (valorable) /liliExcelente capacidad de redacción /liliCapacidad de trabajo en equipo /liliEmpatía con público objetivo mayor de 50 años /li /ul /p #J-18808-Ljbffr

ph3Responsibilities /h3 ul liImpulsar y coordinar proyectos estratégicos dentro del área KAM /li liAsegurar que la información, acciones y equipos avancen alineados para alcanzar los objetivos definidos /li liCoordinar proyectos vinculados al área de grandes cuentas y canal comercial /li liDar soporte en procesos de reporting y análisis de información para la toma de decisiones /li liColaborar con diferentes departamentos para asegurar el correcto desarrollo de las iniciativas en curso /li liRealizar seguimiento de acciones, plazos y compromisos para garantizar el éxito de los proyectos /li liParticipar en iniciativas estratégicas que contribuyan al crecimiento y evolución de la compañía /li /ul h3Qualifications /h3 ul liCapacidad organizativa y gestión de múltiples prioridades /li liHabilidades de comunicación y relación interpersonal /li liMentalidad analítica /li liPrecisión y orientación al detalle /li liFlexibilidad y ganas de aprender /li liFormación en Administración, Marketing, ADE o estudios superiores similares /li /ul /p #J-18808-Ljbffr

pSyneos Health seeks a Medical Writer to serve as MLR Technical Reviewer / Scientific Expert in Spain. The role focuses on ensuring scientific accuracy, data integrity, and proper referencing across assets, collaborating with global teams to comply with guidelines. /ppYou will review content for regulatory compliance, support reference tagging in Veeva Vault, and monitor asset quality data to aid agency reporting. Proficiency in Portuguese and French is required for this FSP position. /p #J-18808-Ljbffr

Welcome to Remedy Edge Spain. We activate potential, amplify with creativity, and accelerate outcomes. Remedy Edge brings strategic thinking and bold communications to healthcare — cutting through the noise to move people and change results. We don't do comfortable. We do cutting edge. Join us and GET THE EDGE. La información a continuación detalla los requisitos del puesto, la experiencia esperada del candidato y las cualificaciones correspondientes. About the role As a Senior Medical Writer, you will take a leading role in developing scientifically rigorous and creatively engaging communication materials that support clients’ medical and promotional strategies. You will act as a trusted expert for both internal teams and clients, providing strategic scientific input, guiding junior writers, and ensuring excellence from concept to delivery. Key Responsibilities • Lead the development of scientific content, ensuring alignment with client goals, brand strategy, and industry best practices., • Provide strategic scientific direction during content planning and campaign execution., • Conduct and oversee bibliographic research, ensuring all materials are accurate, evidence-based, and compliant., • Write, edit, and adapt complex scientific materials—including slide decks, monographs, publications, and training documents—maintaining clarity, accuracy, and adherence to guidelines., • Oversee the preparation and delivery of complete reference sets using Veeva, ensuring quality and compliance., • Manage client feedback processes, ensuring timely integration and consistency across deliverables., • Build and maintain relationships with Key Opinion Leaders (KOLs) to support content development and approvals., • Mentor junior writers, providing feedback, guidance, and support in skill development., • Represent the medical writing function in client meetings, contributing to strategic discussions and providing scientific expertise. About you • Must have a health science degree (e.g. in biology, pharmacy or medicine). PhD is a plus., • 5 years of experience in medical writing and scientific content supervision in marketing and advertising contexts., • Ability to communicate medical/technical information to a wide variety of audiences., • Ability to work in a deadline-driven environment., • Attention to detail and absolute reliability in meeting delivery deadlines., • Team player who can foster positive relationships between the department and other agency teams, such as creatives and account managers. xcskxlj, • Experience with reference managers such as EndNote is a plus. #J-18808-Ljbffr

Location ¿Todo listo para enviar su solicitud? Asegúrese de comprender todas las responsabilidades y tareas asociadas a este puesto antes de continuar. Barcelona or Madrid About the Role As a Senior Medical Writer, you will take a leading role in developing scientifically rigorous and creatively engaging communication materials that support clients’ medical and promotional strategies. You will act as a trusted expert for both internal teams and clients, providing strategic scientific input, guiding junior writers, and ensuring excellence from concept to delivery. Key Responsibilities • Lead the development of scientific content, ensuring alignment with client goals, brand strategy, and industry best practices., • Provide strategic scientific direction during content planning and campaign execution., • Conduct and oversee bibliographic research, ensuring all materials are accurate, evidence-based, and compliant., • Write, edit, and adapt complex scientific materials—including slide decks, monographs, publications, and training documents—maintaining clarity, accuracy, and adherence to guidelines., • Oversee the preparation and delivery of complete reference sets using Veeva, ensuring quality and compliance., • Manage client feedback processes, ensuring timely integration and consistency across deliverables., • Build and maintain relationships with Key Opinion Leaders (KOLs) to support content development and approvals., • Mentor junior writers, providing feedback, guidance, and support in skill development., • Represent the medical writing function in client meetings, contributing to strategic discussions and providing scientific expertise. About You • Must have a health science degree (e.g., in biology, pharmacy or medicine). PhD is a plus., • 5 years of experience in medical writing and scientific content supervision in marketing and advertising contexts., • Ability to communicate medical/technical information to a wide variety of audiences., • Ability to work in a deadline-driven environment., • Attention to detail and absolute reliability in meeting delivery deadlines., • Team player who can foster positive relationships between the department and other agency teams, such as creatives and account managers., • Experience with reference managers such as EndNote is a plus. Omnicom Health is committed to hiring and developing exceptional talent. We agree that talent is uniquely distributed, and we’re focused on developing inclusive teams that can bring the best solutions to everything we do. We strongly believe that celebrating what makes us different makes us better together. xcskxlj Join us—we look forward to getting to know you. We will process your personal data in accordance with our Recruitment Privacy Notice. #J-18808-Ljbffr

A global leader in clinical research services is seeking a Translation Project Manager for Regulatory Submissions in Barcelona. This role involves managing the translation and localization of regulatory submissions, ensuring quality and compliance throughout the project lifecycle. Candidates should possess relevant project management experience within the language services industry and have strong communication skills.br#J-18808-Ljbffr

Medical Writer - MLR Technical Reviewer / Scientific Expert - FSP in 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.The MLR Technical Reviewer will be responsibl

Support localized strategy: Set content goals, add local insights, monitor competitors' content, and help support content direction based on regional insights and cultural nuances. Your day-to-day /h3 ul liCreate perform: Record engaging, informative videos (long‑form and Shorts) that bring our e

Está pensando en solicitar este empleo? No se demore, desplácese hacia abajo y envíe su solicitud lo antes posible para no perder la oportunidad.Manager, Automation & Reporting in Barcelona to lead a global team focused on data insights and robust reporting capabilities.The role involves overseei