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Iwantalent busca un Responsable de Contabilidad y Reporting para liderar el área financiera en una compañía internacional del sector asegurador, con presencia en España, Francia e Italia y coordinación con la matriz en Reino Unido. Se requiere sólida experiencia en IFRS 17, Solvencia II y PCEA, y capacidad para dirigir equipos en un entorno de transformación. Con 6-8 años de experiencia en puestos financieros del sector asegurador, el perfil gestionará cierres, cuentas anuales, reporting #J-18808-Ljbffr

A leading renewable energy operator is seeking a professional to ensure compliance with Quality, Health, Safety, and Environmental (QHSE) standards during project construction and operations. The role involves supporting ISO 9001, ISO 14001, and ISO 45001 management systems and participating in environmental monitoring. Join a pioneering team dedicated to energy transition and sustainability, offering a positive work environment and flexible compensation. #J-18808-Ljbffr

IGNEO Ingeniería Sostenible S.L.U. busca un Controller Corporativo/a con sólida base contable y experiencia en consolidación financiera internacional, para coordinar cierres y el EBITDA consolidado. La posición es 100% presencial en Tres Cantos (Madrid), con incorporación inmediata y proyección de crecimiento dentro del área financiera del grupo multinacional orientado a proyectos. Perfil técnico, analítico y estructurado, con experiencia en IFRS, SAGE y Lucanet. #J-18808-Ljbffr

Analista Control y ReportingApplylocations: Madrid Cristalia, Spaintime type: Full timeposted on: Posted 2 Days Agojob requisition id: R20062144## Job Description SummarySomos una de las aseguradoras más importantes del mundo, formada por personas positivas, dinámicas y comprometidas que hacen que las cosas ocurran. Creemos que nuestra diversidad aporta valor a los equipos, a nuestra cultura y a los clientes. Sabemos que las mejores ideas y soluciones surgen en entornos inclusivos donde todos nos sentimos vistos, escuchados y valorados para que podamos desarrollar nuestro máximo talento. Hemos sido reconocidos como uno de los mejores lugares para trabajar en España por la lista Forbes y el ranking de Actualidad Económica, y es que contamos con la mejor propuesta de valor para todos los que formamos parte de Aegon:## Job Description Apostamos por la flexibilidad a través de nuestro modelo de trabajo híbrido: contamos con la posibilidad de teletrabajar al menos tres días por semana y también de compartir tiempo en unas oficinas adaptadas a la metodología ágil. Te ayudamos a conciliar y desconectar, con flexibilidad horaria durante todo el año y jornada intensiva en el verano. Las mejores acciones para tu bienestar físico y mental (seguro de salud gratuito, fisioterapia en la oficina, iniciativas de vida saludable, etc.) y un gran abanico de beneficios y ventajas sociales (la empresa hace una alta aportación a tu plan de pensiones, seguro de ahorro para la jubilación, retribución flexible, ayudas a la formación, regalo de Navidad, etc.). Oportunidades de desarrollo a todos los niveles mediante proyectos transversales e internacionales. Contamos con acciones de reconocimiento, compensación variable para todos y feedback continuo. Nuestro modelo de gestión está basado en tener conversaciones de calidad de manera recurrente, donde tendrás un papel protagonista. Cultura: el 80% de empleados estamos orgullosos de trabajar en Aegon. Somos una empresa internacional, cercana y empáticaLa oportunidad laboral de tu vida¿Te gustaría ayudar a las personas a vivir su mejor vida?, es a lo que nos dedicamos en nuestro día a día. Lo logramos gracias a que somos una empresa de personas que cuidan de personas, con curiosidad, conectados con la realidad que nos rodea y centrados en dejar un mundo mejor de como lo hemos encontrado. Siempre aprendemos de nuestros clientes y de las demás personas.¡Esperamos que te apasione tanto como a nosotros!(ツ)En Aegon apostamos por la innovación en nuestros procesos de selección. Por ello, te ofrecemos la posibilidad de realizar una primera entrevista telefónica a través de Inteligencia Artificial (Clara IA), lo que nos permite garantizar una experiencia más ágil y una evaluación objetiva y consistente de todas las candidaturas. Nuestra solución cumple con los más altos estándares de seguridad y privacidad de datos.Si quieres participar en este proceso con IA, puedes acceder a través del siguiente enlace: https://app.clara.works/a/j-SDXp6zR9GB8e0vCrXh3Amie_cljuSBq2YlTaSsl7HA?utm_source=clara_works_linkSi prefieres seguir el proceso tradicional, simplemente inscríbete en esta oferta y continuaremos tu candidatura por los canales habituales, sin necesidad de acceder al enlace anterior. (ツ) Sobre la posición:Formarás parte del equipo de Planificación y Análisis Financiero, contribuyendo activamente a la definición, seguimiento y análisis de la evolución del negocio en España.Entre tus principales responsabilidades estarán: Elaborar, analizar y realizar el seguimiento del presupuesto de las entidades del Grupo Aegon en España. Analizar los principales KPIs comerciales, financieros y operativos, identificando tendencias, desviaciones y oportunidades de mejora. Generar insights que apoyen la toma de decisiones estratégicas del negocio. Impulsar la automatización y transformación de los procesos de presupuestación, control de gestión y reporting.* Participar en proyectos de mejora continua orientados a incrementar la eficiencia y calidad de la información.Sobre ti: Experiencia de al menos 5 años en funciones de planificación, control de gestión, análisis financiero o reporting dentro del sector asegurador. Conocimiento de normativa contable US GAAP y/o IFRS 17. Formación universitaria en Actuariales, ADE, Economía o titulaciones afines. Se valorará formación complementaria en Data Analytics, Business Intelligence o similares. Sólida capacidad analítica y experiencia en la interpretación de información financiera y de negocio para la elaboración de informes y recomendaciones. Conocimiento profundo del negocio asegurador y de sus principales indicadores de gestión. Experiencia en explotación, análisis e interrelación de grandes volúmenes de datos. Conocimientos de Python y experiencia en automatización de procesos, informes y cuadros de mando. Nivel avanzado de Excel y experiencia trabajando con modelos financieros. Capacidad para trabajar de forma transversal con diferentes áreas, gestionar múltiples prioridades y desenvolverse en entornos dinámicos. Se valorará un nivel avanzado de inglés y conocimientos de SAP, Power BI y/o SAS. #J-18808-Ljbffr

Turboiber S.L. busca un Responsable de Control Administrativo para impulsar el área financiera y su analítica. Liderarás el diseño de reporting, supervisarás costes y contribuirás a decisiones estratégicas mediante un análisis riguroso de márgenes y eficiencia operativa. Trabajarás en un entorno estable, con interlocución directa con dirección y oportunidades de desarrollo. Se valorará orientación al negocio, proactividad y capacidad para trabajar transversalmente con distintas áreas. #J-18808-Ljbffr

Global Business Services (GBS) aspires to be the Partner of Choice for Suntory Global Spirits, creating exceptional value through the superior delivery of business services and solutions. The International Financial Reporting & Statutory Compliance Lead – Record to Report role is a critical retained organization position responsible for overseeing statutory reporting governance, external reporting support, audit coordination, and complex accounting activities across international operations. This role ensures effective financial governance, compliance, and oversight of Record-to-Report processes while partnering closely with the outsourced BPO provider, regional finance leadership, auditors, and external stakeholders. The position supports the integrity of financial reporting through oversight of trial balance reviews, journal entry governance, reconciliation certification, statutory compliance activities, and audit support. The role collaborates cross-functionally with regional Finance, Tax, Treasury, Controllership, and the BPO provider to ensure accurate, timely, and compliant financial reporting across diverse international markets. Role Responsibilities Prepare and maintain the local statutory books for Beam Suntory Spain, ensuring compliance with Spanish GAAP, IFRS and applicable local statutory accounting requirements. Own and coordinate the preparation of statutory financial statements and supporting documentation for Beam Suntory Spain. Lead retained organization oversight for international statutory reporting, external reporting support, and financial governance activities Support statutory audit activities and coordinate interactions with external auditors across international markets Provide oversight and support for external reporting requirements, ensuring compliance with corporate and local reporting obligations Review and approve non-routine and ad hoc journal entries impacting statutory, management, and general ledger reporting Approve correcting entries, post-close adjustments, and top-side journal entries in accordance with corporate accounting policies Review, certify, and approve balance sheet reconciliations and related supporting documentation Review trial balances for accuracy, completeness, and compliance with accounting standards and corporate policies Finalize and approve final trial balances for reporting and close activities Partner with the BPO provider to ensure timely execution of transactional accounting and close support activities Ensure compliance with internal controls, accounting policies, SOX requirements, and financial governance standards Coordinate with regional and global finance stakeholders to resolve accounting issues, reporting exceptions, and audit findings Monitor key performance indicators (KPIs), close metrics, audit observations, and service level agreements (SLAs) Drive continuous improvement initiatives focused on standardization, automation, close optimization, and reporting efficiency Support audit remediation activities, compliance initiatives, and internal control enhancements Collaborate with Finance, Tax, Treasury, Internal Audit, and external advisors to support regulatory and statutory requirements Support region-specific reporting and compliance considerations across international markets, including local accounting and statutory requirements where applicable Maintain detailed documentation of approvals, reconciliations, audit support materials, and financial governance activities to support compliance and audit requirement Flexibility and willingness to travel internationally, on a quarterly basis or as required by business needs. Qualifications Bachelor’s Degree or equivalent experience in Accounting, Finance, or related field CPA, CA, ACCA, or equivalent professional accounting certification preferred Minimum of 5 years of experience in financial reporting, Record-to-Report operations, controllership, audit, or accounting operations Experience supporting international operations and cross-cultural stakeholder environments preferred Experience supporting retained finance organizations and/or shared services operating models preferred Strong understanding of financial reporting, general ledger accounting, statutory compliance, reconciliations, and internal controls Experience supporting statutory audits, external reporting, and auditor interactions Experience partnering with outsourced service providers or business process outsourcing (BPO) organizations preferred Strong knowledge of accounting standards, close processes, and financial governance frameworks Experience with ERP systems such as SAP and reporting/analytics tools Advanced MS Excel, MS PowerPoint, and Microsoft Office capabilities Strong analytical, problem-solving, and stakeholder management capabilities Ability to work effectively across multiple international markets and collaborate with global stakeholders Experience driving process improvements, automation initiatives, and governance standardization in a shared services environment Strong knowledge and demonstrated experience in Spanish GAAP, IFRS and Spanish statutory accounting and reporting requirements. Hands‑on experience in the preparation of local statutory books and financial statements in Spain. #J-18808-Ljbffr

Collaborating with Editors, Staff Writers, and the video and social team to establish and maintain high editorial standards, adhering to the brand's identity and tone of voice. Reporting directly to our VP of Media, you will play a pivotal role in managing a growing team of passionate editors, write

Collaborating with Editors, Staff Writers, and the video and social team to establish and maintain high editorial standards, adhering to the brand's identity and tone of voice. You will also be responsible for coordinating, assigning, and prioritizing editorial work within the team, collaborating wi

Italian Creative Copywriter (native speaker) DDB Spain in Madrid, MD, ES. Perfil En TBWA-DDB Madrid buscamos un/a Creative Copywriter nativo/a en italiano para trabajar con una importante marca del sector financiero, que opera de forma digital en Italia (el idioma habitual en la oficina será españ

Tether is seeking a Technical Content Creator to demonstrate the practical power of its peer-to-peer stack. This builder-centric role targets engineers who bridge low-level infrastructure, cryptography, and applications. You will write code, spin up nodes, and record polished demos. Create ongoing visual prototypes that prove decentralized, serverless infra in action, collaborating with core teams across Pear and Bare. #J-18808-Ljbffr

Zurich Insurance Group, via ServiZurich in Barcelona, seeks an experienced Investment Accounting & Reporting Associate Director to join the IAA function. You will lead the investment subledger, ensure accurate valuation, and drive close processes and regulatory reporting. You will apply IFRS, US GAAP, and US Tax rules, coordinating with Finance and Investment teams while advancing automation and data analytics capabilities. #J-18808-Ljbffr

Booksy is seeking a senior accounting professional to own group consolidation, intercompany charges, and IFRS/US GAAP reporting across international entities. You will drive accuracy in trial balances, implement consolidation tooling, and support audits while mentoring finance teams in a rapidly growing startup environment. Ideal candidates bring 4+ years of consolidation experience, ACCA/CIMA/CPA, and advanced Excel in a remote-first global company based in Spain. #J-18808-Ljbffr

Wizeline is seeking a talented software engineer to develop and enhance a translation platform and related services, integrating AI/LLM-based translation capabilities into Dow Jones’ content-processing ecosystem. You will build reliable APIs and services for translation requests, support event-driven processing, and work with Dow Jones engineers on technical design, testing and documentation. This role offers a flexible, remote-friendly environment with opportunities for global mobility and #J-18808-Ljbffr

Appodeal, Barcelona-based, seeks an senior FP&A leader to own the consolidated operating model, board reporting, and monthly forecasting. Youll coordinate with Accounting, Product, and Growth teams while driving automation and scenario planning. The role requires strategic financial thinking and a track record of influencing leadership. The position offers a hybrid work rhythm in Barcelona with exposure to global revenue streams and a fast-growing ad-tech environment. #J-18808-Ljbffr

We are a Scale up in a hyper growth phase. As our Director of Group Controlling and Accounting , you will be the guardian of our global financial integrity. We are looking for a leader with exceptional technical rigor who has already operated in complex corporate environments and knows how to transform traditional processes into an automated, efficient financial machine. Your mission will be to lead the international control and consolidation structure, ensuring our financial information under IFRS standards is impeccable, while scaling and mentoring a high-performance team. Responsibilities: Global Consolidation & IFRS Mastery Lead the monthly, quarterly, and annual consolidation process for all Group entities. Ensure all financial statements strictly comply with IFRS standards and local GAAPs. Act as the internal technical expert for complex transactions, ensuring "investment-ready" financial reporting. Automation & Process Improvement Spearhead the transformation and automation of Accounting and Reporting processes to significantly reduce time-to-close. Optimize the use of the ERP and BI tools to eliminate manual tasks and guarantee a "single source of truth" for financial data. Implement continuous improvement methodologies for accounting workflows between subsidiaries and headquarters. Leadership & Team Management Direct, mentor, and scale the central accounting and control team. Establish clear KPIs for the team and foster a culture of operational excellence and professional development. Coordinate with local finance heads in each market, ensuring seamless communication aligned with Group objectives. Audit, Tax & Compliance Serve as the primary strategic point of contact for external auditors, leading the annual audit process to a clean opinion. Design and implement a robust internal control framework to mitigate risks in a hyper-growth environment. Support M&A activities and future funding rounds by leading financial Due Diligence and Data Room preparation. Requirements: Experience: +10 years of solid track record. Essential experience as a Group Controller in large corporate or multinational environments, following a strong foundation in external audit. IFRS Expert: Proven expertise in preparing consolidated financial statements under IFRS regulations. Leadership: Demonstrated experience in managing direct teams and the ability to inspire technical profiles. Digital Mindset: Passion for finance technology; experience in ERP implementation/optimization and reporting automation tools. Languages: Expert level in English and Spanish Due to the impossibility of providing sponsorship, we require you to have the eligibility to work in the EU. #J-18808-Ljbffr

AgileEngine is an Inc. 5000 company that creates award-winning software for Fortune 500 brands and trailblazing startups across 17+ industries. We rank among the leaders in areas like application development and AI/ML, and our people-first culture has earned us multiple Best Place to Work awards. WHY JOIN US If you're looking for a place to grow, make an impact, and work with people who care, we'd love to meet you! ABOUT THE ROLE We are looking for a Senior Technical Writer to design and automate AI-driven software documentation for end users, developers, and system integrators. MUST HAVES 4+ years of technical writing experience , with demonstrated expertise in software documentation (SaaS, cloud platforms, or developer-focused content). • Deep familiarity with prompt engineering and ability to design effective prompts, configure AI tools, and iterate based on output quality to achieve consistent documentation. • Strong understanding of documentation architecture and information design. Ability to analyze different documentation types and design patterns that scale., • Technical comfort with APIs, event streaming, batch processing, system architecture, and data models . Ability to understand complex concepts and write documentation that captures them accurately. • Proficiency with Markdown, YAML, Git, and version-controlled workflows . Comfortable in code editors and command-line environments. • Strong written and verbal communication skills, with an ability to write clear, user-centered documentation and communicate technical concepts to diverse audiences., • Attention to detail and excellent organizational skills with the ability to manage multiple priorities and maintain consistency across documentation systems., • Problem-solving mindset with ability to think critically about processes and advocate for improvements to documentation systems and workflows., • Experience in fast-paced, cross-functional product environments with the ability to adapt to changing priorities., • Bachelor's degree in computer science, English, or a related field, or equivalent work experience. NICE TO HAVES • Loyalty product, MarTech, or B2B SaaS experience preferred., • Redocly documentation framework for API references. WHAT YOU WILL DO • Partner with product, engineering, and operations teams to understand documentation needs and user workflows, then design documentation architecture and automation patterns that serve multiple audiences – end users, developers, and system integrators., • Establish documentation standards and build governance and quality gates directly into the automation system to ensure all generated documentation – user guides, API documentation, integration guides, in-product help, and release notes – maintains consistency and user value., • Build and refine prompt templates, style guides, and content models that enable developers and writers to generate consistent, high-quality documentation at scale., • Write, edit, and review documentation to model excellence, validate automation output quality, and identify patterns that strengthen prompts and templates., • Measure documentation impact using analytics and user feedback to identify gaps and inform improvements to the automation system, content strategy, and documentation approach., • Document all systems, configurations, prompts, and decision logic thoroughly so the team can maintain, evolve, and improve the automation system independently. PERKS AND BENEFITS Professional growth : Mentorship, TechTalks, and personalized growth roadmaps. Competitive compensation : USD-based pay with education, fitness, and team activity budgets. Exciting projects : Modern solutions with Fortune 500 and top product companies. Flextime : Flexible schedule with remote and office options. Meet Our Recruitment Process Each step helps us understand your skills and overall fit. If it’s a match, you’ll receive an offer. #J-18808-Ljbffr

Impala Terminals Group in Madrid seeks a Financial Reporting Controller to support accounting processes with IFRS expertise, focusing on compliance, financial reporting and internal controls. You will manage month-end close, coordinate with auditors and tax teams, and provide analysis to senior management. Fluency in English and strong analytical skills required in an international context. #J-18808-Ljbffr

IQVIA is seeking a Consultant Medical Writer to support the Global Health Economics team in HTA evidence and value communications. You will write HEOR and payer materials, contribute to GVDs and HTA dossiers, and collaborate with a senior team to manage small workstreams and ensure high-quality outputs. The role requires fluency in English, strong scientific writing, and the ability to translate complex data into compelling payer-focused narratives for EU, UK, and global markets. #J-18808-Ljbffr

About Impress We believe everyone deserves a smile they'll love. We are IMPRESS, the largest chain of digital orthodontic clinics in Europe, revolutionizing the invisible orthodontic sector and bringing smiles to people's faces. Our unique combination of medical expertise and digitalization has earned us recognition as one of the top fastest-growing Health Tech companies by Forbes. Born in Barcelona in 2019, we have expanded across 10 countries with more than 110 locations, offering leading care and state-of-the-art technology. The role We are looking for a Group Consolidation & Reporting Manager to run the consolidation and external financial reporting of a complex, multi-entity, multi-jurisdiction group under IFRS. You will be a key technical contributor on group reporting and a day-to-day contact for our external auditors, working closely with local finance teams across our markets. This is a hands-on role: you will be close to the numbers and the process every day. What you will do: Run the group consolidation process across all entities and jurisdictions under IFRS Prepare consolidated financial statements and group reporting packages Support the group audit to close — day-to-day contact for external auditors, managing audit requests, timelines and technical queries Apply IFRS technical accounting positions and help ensure consistent application of group accounting policy across markets Help improve and scale consolidation processes, controls and tools as the group grows Partner with local finance teams to ensure quality and timeliness of reporting inputs Support management and board reporting with reliable, audit-ready numbers What we are looking for: 5+ years in group consolidation and/or audit of consolidated IFRS financial statements, ideally for multinational groups Solid technical knowledge of IFRS and multi-entity consolidation Experience working with external auditors through an audit cycle Big Four or audit-firm training a plus Fluent English (our working language); additional European languages a plus Hands-on, detail-driven, and comfortable in a fast-paced, high-complexity environment Qualified or part-qualified accountant (ACCA / ACA / CPA / equivalent) preferred What we offer A high-impact role at the core of group reporting for a fast-growing European group Central role in Barcelona-based finance team with international scope Competitive compensation based on experience Real scope to grow with the consolidation function as it scales At Impress we cultivate a culture of inclusion and diversity. We celebrate our employees' individual strengths, views, and experiences and we encourage all candidates to apply, without regard to race, color, religion, gender identity, sexual orientation, age, national origin, disability, or any other factor. Our differences enable us to be a better team - one that makes better decisions, drives innovation, and delivers better results. #J-18808-Ljbffr

ICF is seeking a Project Finance Analyst to join our Europe & Asia Business Management team on a permanent basis to drive financial performance of the ICF activities. The role covers forecasting, revenue profiling, budgeting, and close collaboration with Project Managers and Directors across diverse teams. You will manage project financials, sub-contractor accruals, and client billing, supporting timely month-end reporting and WIP reduction. #J-18808-Ljbffr

A Frulact procura um/uma Finance Controller para o departamento de Finance and Risk Management na Maia. O/ a candidato(a) ideal tem formação superior em áreas relacionadas e experiência em tesouraria, SAP e BI, com forte capacidade de organização. Será responsável pela gestão diária de tesouraria, fluxo de caixa, gestão de instrumentos financeiros e apoio a melhorias de reporting. O cargo é em regime integral, com foco na liquidez e governança financeira do grupo. #J-18808-Ljbffr

Madrid, Barcelona Full‑time Your mission Are you passionate about finance and business? We are looking for a full‑time Senior Financial Content Consultant to join us in ahybrid role based in Madrid.We are seeking a talented professional who can transform complex financial products, investment tr

Catalonia Hotels & Resorts busca un Responsable de Consolidación para su Headquarters en Barcelona. Será el titular del proceso de consolidación y reporting mensual, coordinando las sedes internacionales y transformando estados contables a IFRS. Se valorará experiencia en Big4 o multinacionales y dominio de SAP. El puesto requiere grado en ADE/Economía y al menos 3 años en funciones similares, con rigor y capacidad de trabajar con plazos ajustados. #J-18808-Ljbffr

About Accelerant Accelerant is a data-driven risk exchange connecting underwriters of specialty insurance risk with risk capital providers. Accelerant was founded in 2018 by a group of longtime insurance industry executives and technology experts who shared a vision of rebuilding the way risk is exchanged – so that it works better, for everyone. The Accelerant risk exchange does business across more than 20 different countries and 250 specialty products, and we are proud that our insurers have been awarded an AM Best A- (Excellent) rating. For more information, please visit www.accelerant.ai. About Accelerant Accelerant is a data-driven risk exchange connecting underwriters of specialty insurance risk with risk capital providers. Accelerant was founded in 2018 by a group of longtime insurance industry executives and technology experts who shared a vision of rebuilding the way risk is exchanged – so that it works better, for everyone. The Accelerant risk exchange does business across more than 20 different countries and 250 specialty products, and we are proud that our insurers have been awarded an AM Best A- (Excellent) rating. For more information, please visit www.accelerant.ai. About The Role This is a rare opportunity to join a Solvency II reporting function that is actively investing in how it works — not just maintaining what already exists. As a Senior Analyst, you'll bring deep SII expertise to a team that is mid-journey on a genuine modernization program, with Tagetik at the center of its reporting infrastructure and a real appetite for automation and AI-driven process improvement. You'll have meaningful ownership across the reporting cycle, from QRT production and regulatory change through to capital calculations and audit-ready controls — and you'll be expected to shape how the function evolves, not just run it. If you're a few years into your SII career and looking for a step up that offers both technical depth and broader influence, this role is worth a close look. Key Responsibilities Regulatory Reporting & Compliance Own the end-to-end annual reporting schedule, driving data sourcing, QRT population and timely delivery in line with PRA and EIOPA requirements Stay ahead of regulatory change — monitor taxonomy updates from the PRA and EIOPA and take accountability for ensuring QRTs reflect the latest requirements Capital & Actuarial Calculations Take ownership of SCR calculations as a core member of the Capital Management team, contributing technical depth to the wider actuarial and finance functions Data, Controls & Audit Maintain a robust data lineage framework spanning all aspects of the Solvency process, partnering with data, finance and business engagement teams to stay ahead of changes to upstream data flows Maintain auditable controls and clear process documentation that stand up to internal and external scrutiny Drive the control framework forward, including peer review, to ensure the function is consistently audit-ready Systems & Automation Play a leading role in the build-out of automation within Tagetik, working directly with system consultants to translate reporting knowledge into scalable solutions Act as the team's AI advocate — identifying credible opportunities to automate processes and controls and helping move them from idea to implementation Process Improvement Continuously challenge the status quo, identifying and delivering process improvements that reduce manual effort and increase the reliability of the reporting cycle Stakeholder Engagement & Communication Build trusted relationships across data, finance and business teams, positioning yourself as the go-to person for Solvency data and process questions Lead quarterly discussion forums with senior stakeholders across the full Solvency reporting chain, communicating complex regulatory and technical topics with clarity and confidence What We're Looking For, +5 years of hands‑on Solvency II reporting experience Strong working knowledge of QRT production, regulatory submissions and PRA/EIOPA requirements Experience with or exposure to Tagetik or a comparable reporting platform Familiarity with SCR calculations and Solvency II Best Estimate/Risk Margin, or a solid enough actuarial/finance grounding to engage credibly with Capital Management colleagues A track record of building controls and documentation that hold up under audit scrutiny Strong communicator — comfortable presenting to senior stakeholders and managing relationships across functions Genuine curiosity about process improvement and emerging technology, including AI Why join us, A reporting function with real modernization underway — Tagetik investment, automation ambition and an open mind on AI Genuine ownership at Senior Analyst level, with visibility across the full SII cycle A collaborative team that values technical rigor and continuous improvement in equal measure #J-18808-Ljbffr

Workday in Spain seeks an experienced Workday consultant to deliver Success Plans services and enable customers to maximize their Workday investments. The role requires 5+ years in IT implementation with Workday Financials Reporting, plus 2+ years in software consulting. A Workday Certification or ability to certify in one area is required; a Bachelor’s degree is essential, with advanced degrees preferred. #J-18808-Ljbffr

IQVIA is seeking a senior Medical Writer to deliver high-quality clinical documents for eye health and inflammatory indications. You will integrate with sponsor teams, manage timelines, and ensure adherence to regulatory requirements across ICH, FDA, and EMA guidelines. The role emphasizes senior-level writing leadership, collaboration across disciplines, and adherence to sponsor SOPs while using eDMS and structured authoring tools for accurate document delivery. #J-18808-Ljbffr

Puig SL, based in Barcelona, seeks an Accountant Executive (Greek Appreciated) to support global finance operations. You will manage month-end closes, balance sheet accuracy, cash forecasting, tax reporting, and statutory audits while collaborating with local controllers and external auditors. The role requires 3–5 years’ accounting experience, a degree in accounting, and fluency in English; Greek is a plus. Proficiency in SAP and MS Office is essential for success. #J-18808-Ljbffr

HBX Group is a world-leading technology partner for travel, combining finance leadership with a tech-first mindset. This role focuses on statutory reporting, audits, financial controls, and balance sheet governance for assigned entities to ensure local GAAP compliance and reliable regional reporting. You will collaborate with Global Finance Services, support tax reporting, and help strengthen internal controls across the finance function while working closely with the Head of Finance. #J-18808-Ljbffr

A dynamic real estate investment platform is seeking a Senior Accounting Manager to oversee accounting operations, ensure compliance with Spanish GAAP, and lead financial reporting for multiple entities. The role includes managing day-to-day activities, interacting with auditors and stakeholders, and improving accounting processes. Ideal candidates will have a Bachelor's in a relevant field, 5–8 years of experience, and strong Excel skills. This position offers competitive compensation and the chance to work in a fast-paced environment. #J-18808-Ljbffr

Olixir Spain, part of Omnicom Health, is seeking a Medical Writer to develop scientific content—from slide decks to monographs, abstracts, and congress reports—for diverse audiences. You will devise publication strategies, conduct bibliographic research, write materials, and provide complete reference sets, incorporating client feedback and coordinating with KOLs and cross-functional teams to ensure timely delivery. #J-18808-Ljbffr

Senior Medical Writer - Europe / home based - FSP TeamSyneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need.Discover what your 25,000 future colleagues already know:Why Syneos Health• We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.• We are committed to building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life.• We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.Job ResponsibilitiesThis is a full-time permanent position within our FSP Team. For this role, we can consider candidates based anywhere in EMEA except Switzerland, Germany and France.Leads the clear and accurate completion of medical writing deliverables, ensuring scientific information is presented clearly and accurately. Manages medical writing activities associated with individual studies, coordinating medical writing activities within and across departments with minimal supervision. Leads the resolution of comments from the client.Completes a variety of documents that may include clinical study protocols and clinical study protocol amendments; clinical study reports; patient narratives; annual reports; investigator brochures; informed consents; annual reports; plain language summaries; periodic safety update reports, clinical development plans; IND submissions; integrated summary reports; NDA and eCTD submissions; journal manuscripts; and abstracts, posters, and presentations for scientific meetings.Adheres to established regulatory standards, including, but not limited to, ICH E3 guidelines, as well as company standard operating procedures, client standards, and company and/or client approved-templates, authorship requirements, and style and formatting guides, when completing medical writing projects, on time and on budget.Coordinates quality and editorial reviews. Ensures source documentation is managed appropriately. Leads team document reviews, and reviews documents as needed.Acts as peer reviewer for internal team to ensure document scientific content, clarity, overall consistency, and proper format.Reviews statistical analysis plans and table/figure/listing specifications for appropriate content, and for grammar, format, and consistency. Provides feedback to further define statistical output required and document needs.Interacts and builds good working relations with clients, department head, and peers in data management, biostatistics, regulatory affairs, and medical affairs, as necessary, to produce writing deliverables.Performs online clinical literature searches and complies with copyright requirements.Identifies and proposes solutions to resolve issues, escalating as appropriate. Provides technical support, training, and consultation to department and other company staff. May contribute to development of internal materials and presentations or changes to internal process, standard practices, and capabilities.Mentors and leads less experienced medical writers on complex projects, as necessary.Develops deep expertise on key topics in the industry and the regulatory requirements and guidelines that affect medical writing.Aware of budget specifications for assigned projects, working within the budgeted hours and communicating status and changes to medical writing leadership.Completes required administrative tasks within the specified timeframes.Performs other work-related duties as assigned.Minimal travel may be required (less than 25%).Qualifications:3-5 years of relevant experience in science, technical, or medical writing.Veeva Vault - MUST HAVEFSP or CRO experience preferredTech Savy - you feel comfortable using technologyExperience working in the biopharmaceutical, device, or contract research organization industry required.Strong understanding of FDA and ICH regulations, other regulatory guidelines, and/or good publication practices strongly required.Experience writing relevant document types required.Extensive knowledge of English grammar and ability to communicate clearly; strong familiarity with AMA Manual of Style.Get to know Syneos HealthOver the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.http://www.syneoshealth.comAdditional InformationTasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. #J-18808-Ljbffr

REMEDY EDGE™ SPAIN in Barcelona is seeking a Medical Writer Supervisor to oversee scientific content development and supervision. The role requires a health science degree and at least 5 years of experience in medical writing and content supervision. Responsibilities include supervising medical strategies and creating scientific materials. The ideal candidate should be a native or bilingual Spanish or English speaker, have strong attention to detail, and be able to manage relationships with Key Opinion Leaders. This position values teamwork and collaboration within a diverse team. #J-18808-Ljbffr

IQVIA LLC seeks a Consultant Medical Writer to join its Global Health Economics HTA Evidence & Strategy Centre of Excellence. You will focus on HEOR/HTA medical writing, producing EU Joint Clinical Assessment dossiers, global value dossiers, and payer materials, collaborating with senior team members to deliver high-quality outputs. You will translate clinical and economic data into compelling payer narratives, support project delivery, and mentor junior writers in a fast-paced, global #J-18808-Ljbffr

About fonio We grew from $1M to $10M ARR in under 12 months and now serve 10,000+ customers. Fonio is Europe’s market leader for AI phone agents for SMBs. Now we’re expanding globally and into new products. We move fast, take ownership, give direct feedback, and avoid politics and unnecessary meetings. Join one of Europe’s fastest-growing companies . Your Role You are the face of fonio. You get in front of the camera, explain AI in a way that gets people excited, and build both brand and conversions at the same time. The challenge: we’re B2B, but we want to build ourselves like a consumer brand. What You’ll Do Regularly produce content for TikTok and Instagram: short, entertaining videos about AI, automation, and our products Contribute ideas, help develop formats, and understand what performs Think brand and conversion together: you know that great content can do both Work closely with our Creative Strategist Who We’re Looking For You feel at home in front of the camera and you’re entertaining on it You’re excited about AI and the whole space, not just casually interested Native-level Italian + good English skills What We Offer Competitive salary: €45,000–€60,000 Equity: you’re helping build this, so you should get a piece of it Equipment of your choice: whatever makes you happy Lunch & dinner on us: We cover your lunch and dinner every day, plus unlimited drinks and snacks. Application Process 15-min intro call 30-min skill interview 20-min culture fit #J-18808-Ljbffr

Tecan in Barcelona, Spain is seeking a Corporate Controller for a 100% role to lead group reporting, budgeting, and forecasting. You will coordinate planning across divisions, prepare analyses for the Management Board and Board of Directors, and drive improvements in reporting and consolidation processes. You will collaborate with FP&A and local finance teams to ensure financial transparency. Ideal candidates have 5–7 years in Controlling, English and Spanish fluency, SAP S/4HANA experience, and #J-18808-Ljbffr

Medical Writer - Future roles (Spain) Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Every day we perform better because of how we work together, as one team, each the best at what we do. We bring a wide range of talented experts together across a wide range of business-critical services that support our business. Every role within Corporate is vital to furthering our vision of Shortening the Distance from Lab to Life®. Discover what our 29,000 employees, across 110 countries already know. Why Syneos Health We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. Job Responsibilities Compiles, writes, edits, and coordinates medical writing deliverables that present scientific information clearly and accurately, and works as a medical writer within and across departments with moderate supervision. Completes a variety of documents that may include clinical study protocols and protocol amendments; clinical study reports; patient narratives; and investigator brochures. Adheres to established regulatory standards, including ICH E3 guidelines, company standard operating procedures, client standards, company and/or client-approved templates, authorship requirements, and style and formatting guides, when completing medical writing projects, on time and on budget. Coordinates quality and editorial reviews. Ensures source documentation is managed appropriately. Leads document reviews, reviews documents as needed, and resolves comments from client. Reviews statistical analysis plans and table/figure/listing specifications for appropriate content and for grammar, format, and consistency. Interacts and builds good working relationships with clients, department head, and peers, as necessary, to produce writing deliverables. Performs online clinical literature searches and complies with copyright requirements. Identifies and proposes solutions to resolve document issues, escalating as appropriate. Continues professional development to grow awareness of industry standards and best practices to improve ability to meet client expectations. Aware of budget specifications for assigned projects, working within the budgeted hours and communicating status and changes to medical writing leadership. Completes required administrative tasks within the specified timeframes. Performs other work-related duties as assigned. Minimal travel may be required (less than 25%). Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. Discover what our Syneos Health colleagues already know: work here matters everywhere. Work alongside the brightest minds in the biopharmaceutical industry taking down walls and removing barriers to speed our customers’ delivery of important therapies to patients. We are strategic thinkers who actively seek different perspectives, whether across offices or across oceans. Because we solve some of the toughest challenges facing the most prestigious healthcare companies today, you'll gain exposure and be supported with comprehensive resources including emerging technologies, data, science and knowledge sharing. The diversification and breadth of Syneos Health creates a multitude of career paths and employment opportunities. We’re a growing, global company dedicated to advancing our talent past their initial role. Discover what our 29,000 employees already know: work here matters everywhere. We work hard, and smart, all in the name of getting much-needed therapies to those who need them most. A career with Syneos Health means your everyday work improves patients’ lives around the world. Selecting us as an employer secures a career in which you’re guaranteed to: Partner with the most diverse team of experts in the industry. From the top down, our people are inspiring. Everyone has a voice and is encouraged to use it. Work in specialized Syneos Health teams that are therapeutically or functionally aligned for expert collaboration. We assemble clinical teams where everyone, from CRAs to senior management, is skilled in the same therapeutic area or customer teams. With this structure, everyone on your team speaks the same language and can deliver unique insights into the therapeutic environment and patient population. We are partners with purpose. We integrate seamlessly with our customers and do what’s best for their success. Our people provide the brilliant ideas, valuable insights and endless energy that accelerates the impact of life changing therapies worldwide. #J-18808-Ljbffr

Workday, Inc. is seeking a seasoned Workday Success Plans professional to help customers maximize value from Workday applications in a fast-paced environment. You will advise on configuration, deliver demonstrations, and guide customers through optimization paths across Go-Live to post-go-live adoption. The role requires strong communication skills, 5+ years in IT implementation with Workday Financials reporting, and the ability to travel up to 20% as needed. Fluency in English is essential. #J-18808-Ljbffr

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. As a Senior Medical Writer at ICON, you will lead the development and execution of medical writing strategies for clinical research projects, contributing to the advancement of innovative treatments and therapies. What You Will Do You will take ownership of medical writing deliverables, applying your expertise to complex challenges. Key Responsibilities Include Independently produces clinical and regulatory documents in collaboration with Principal/Senior Principal MW assigned to the program. These documents may include clinical study level documents such as Clinical Study Protocols or Clinical Study Reports. This includes Phase 1 in patients to Phase 3 across multiple therapeutic areas. Thoroughly analyze and critically interpret data to determine the best approach to composing each document, applying lean writing strategies. Acts as the primary contact for the study team in relation to the preparation and timelines (incl. planning) of assigned documents. Facilitates the review of the documents and ensures that documents are submission-ready and finally approved. When preparing documents you will be directly in contact with QC personnel and publishing specialists who support you in document preparation. Mentoring and coaching junior medical writers, providing guidance on best practices, writing techniques, and scientific principles, and fostering a culture of excellence, collaboration, and continuous learning within the medical writing team. Your Profile You will have a strong foundation in medical writing, with the experience to work independently and guide others. Required Qualifications And Experience 3-5 years of experience as regulatory writer Regulatory experience: Mandatory protocol writing experience in phase II or III, also CSR experience is good to have Bachelor's degree in a relevant scientific discipline or healthcare-related field Proficiency in interpreting and summarizing complex clinical trial data, scientific research findings, and statistical analyses, with excellent writing, editing, and proofreading skills Strong understanding of regulatory requirements (e.g., ICH-GCP, FDA, EMA) governing the preparation and submission of clinical documents and publications, and experience in interacting with regulatory agencies during the review and approval process. Excellent interpersonal and communication skills, with the ability to collaborate effectively with cross-functional teams, build relationships with key stakeholders, and influence decision-making processes. remote What ICON Can Offer You Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our Benefits Examples Include Various annual leave entitlements A range of health insurance offerings to suit you and your family’s needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here #J-18808-Ljbffr

Bridgestone America, Inc. is seeking a Senior Technical Writer to own content across product, engineering, and customer experience. You will manage API references, installation guides, and release communications from drafting through translation and publication. The role demands collaboration with product, engineering, and marketing to ensure accuracy and timely delivery. You should have 5+ years in technical writing for hardware/software, experience with API docs, and strong English writing #J-18808-Ljbffr

May Business Consulting busca un Data Analyst con experiencia en mercados financieros y reporting regulatorio para unirse al área de Market Regulations en Madrid. Participarás en procesos BAU y colaborarás con equipos multidisciplinares para garantizar reportes precisos de DFA y EMIR. Se valorará automatización de procesos y desarrollo de herramientas de análisis, con dominio de Python, SQL y herramientas de procesamiento de grandes volúmenes de datos. Incorporación híbrida en Madrid. #J-18808-Ljbffr

Join our Payments Operations team and help shape the future of regulatory reporting through automation and collaboration. You will work on impactful projects, develop your skills, and contribute to a culture of innovation. At J.P. Morgan, your growth is valued—advance your career while making a difference for our clients and the firm. As a Business Analyst within Corporate and Investment Bank Payments Operations, you will promote automation and execution of EMEA regulatory reporting obligations. You will leverage your analytical skills to support process improvements and key initiatives, collaborating across teams to ensure compliance and operational excellence. Your expertise will help deliver accurate, efficient reporting and foster a culture of continuous improvement. Job Responsibilities: Analyze regulations to identify EMEA reporting requirements and products in scope. Collaborate with subject matter experts, Technology, and Product partners to understand procedures and data sources. Lead business analysis for reporting obligations using Waterfall and Agile best practices. Gather, validate, and own business requirements; write BRDs, define acceptance criteria, perform testing, and raise user stories. Identify process improvements and risk mitigation solutions to strengthen control environments. Conduct walkthroughs with stakeholders to articulate reporting requirements. Execute data analysis, prepare reports, and manage regulatory submissions. Prepare SOPs, document changes, and maintain Confluence wiki content. Participate in department continuous improvement initiatives. Communicate effectively with senior stakeholders on status, progress, issues, and blockers. Proactively self-learn and investigate product designs, systems, and payment flows. Required qualifications, capabilities, and skills: Min. 4 years of experience as a Business Analyst or in a similar role. Proficient in English. Excellent communication and presentation skills across stakeholders. Ability to work effectively with individuals from different departments and areas of expertise. Advanced proficiency in Microsoft Office, including Excel, Visio, and PowerPoint. Ability to analyze data and translate technical information into clear business reports. Strong problem-solving mindset with a structured approach. Demonstrated leadership, responsibility, analytical skills, and self-motivation. Preferred qualifications, capabilities, and skills: Knowledge of SQL, Alteryx, or Python. Additional languages such as Spanish, French, German, or Italian. Experience with JIRA and Confluence. Familiarity with payment systems such as ACH, SEPA, RTP, Wires, and demand deposit accounts. Previous experience in regulatory reporting, business analysis, or process automation within financial services. #J-18808-Ljbffr

J.P. Morgan in Madrid is seeking a Regulatory Operations Associate to support Payments regulatory reporting. You will manage intake requests for new and revised regulations, assess impact, and ensure compliance in a standardized way. Joining the Global Regulatory Operations team, you will collaborate with cross-functional partners, perform weekly scanning of developments, and help deliver key metrics and knowledge base updates. #J-18808-Ljbffr

ENGIE España busca un/a Finance Controller para su sede en Madrid, con 1-3 años de experiencia en controller/FP&A y dominio de SAP/Power BI. Elaborará reporting y cuadros de mando para la gestión de la unidad de negocio. La posición ofrece un entorno híbrido, planes de formación y un sistema de retribución flexible; un equipo multidisciplinar y oportunidades de desarrollo profesional dentro de un grupo energético internacional. #J-18808-Ljbffr

Briolf Group, un grup català amb presència internacional, busca un/a Responsable de consolidació financera per liderar el reporting i els tancaments del grup. La persona seleccionada recollirà informació de les filials, prepararà conciliacions intragrup i col·laborarà amb auditors per millorar processos. S’espera una sòlida experiència en finances i consolidació, capacitat de treball en equip i orientació a dades per donar suport a la direcció financera. #J-18808-Ljbffr

Content Creator (Short-Form Video) Barcelona, Spain Full-time About the role Join our four-person, AI-first email marketing startup in Barcelona to create, film, and edit funny short-form videos about startup life and useful B2B software ideas. Full-time; $70,000 USD gross per year. You'll work directly with our team, turning real moments from building Migma into reels people want to share. You'll also make our AI email product understandable and entertaining for marketers and founders. This is a hands-on creator role, with room to shape our voice and try ideas quickly. What you'll do Pitch and script short videos about our daily startup life, the team, and the product Film with the team in Barcelona and appear on camera when the concept calls for it Edit polished, fast-paced reels with strong hooks, captions, and sound Turn B2B email marketing and AI product ideas into clear, funny stories Publish and learn from performance across Instagram, TikTok, and LinkedIn What we're looking for Strong spoken and written English Based in Barcelona or able to relocate and film with the team regularly Examples of short videos you conceived, filmed, or edited; personal or student projects count Comfortable collaborating on camera and giving others direction Curiosity about startups, AI, and B2B software; prior SaaS experience is welcome but not required What We Offer $70,000 USD gross annual salary for a full-time role Creative ownership with a small team in Barcelona Room to experiment, learn, and build a visible body of work #J-18808-Ljbffr

A global manufacturing company seeks a financial controller based in Spain to manage financial data analysis across multiple entities. You will prepare financial reports, ensure accuracy in reporting, and collaborate with international teams. The ideal candidate has a degree in Finance or Accounting and 2-4 years of experience in financial controlling, along with strong analytical abilities and proficiency in Excel. This is an opportunity to play a vital role in enhancing financial processes and compliance across the organization. #J-18808-Ljbffr

IQVIA is seeking a senior-level FTE Medical Writer to deliver clinical documents across CTRs, protocols, IBs and submission materials with emphasis on eye health and inflammation. The role embeds in sponsor processes, aligning with project teams, timelines, and required trainings. The ideal candidate has ~5 years of medical writing in biopharma or CROs, strong regulatory knowledge (ICH/FDA/EMA), and proven ability to lead complex documentation while maintaining scientific accuracy. #J-18808-Ljbffr

Frankfurt, Hesse, Germany Lisbon, Portugal Brussels, Brussels-Capital Region, Belgium Belgrade, Serbia Barcelona, Spain London, United Kingdom Madrid, Spain Full time R1560755 The FTE Medical Writer will serve as an integrated member of the team, delivering medical writing services for the development of clinical documents, including Clinical Trial Reports (CTRs), Trial Design Outlines/Clinical Trial Protocols (TDOs/CTPs) and CTP amendments, Briefing Books, Investigator’s Brochures (IBs) and IB updates, Biomarker Reports, and submission documents such as the Summary of Clinical Efficacy and Safety, etc. Emphasis will be placed on the therapeutic areas of eye health and inflammation; senior-level experience in these areas is preferred. The FTE Medical Writer will work on a dedicated basis and be embedded in sponsor’s processes and workflows, including Feedback and Alignment Meetings. In this role, the FTE Medical Writer will participate in ongoing project-related activities, such as planning, project discussions, and all required training sessions. The FTE Medical Writer will adopt sponsor’s systems, tools, and methodologies to ensure seamless collaboration and alignment with internal teams. Tasks typically include, but are not limited to: Document management: Set-up and management of clinical document in the Electronic Document Management System (EDMS) Review and approval of the Statistical Analysis Plan in the EDMS Management of timelines including proposal of timelines to trial/project team (based on timelines communicated by sponsor), finalising them after agreement, and updating them as appropriate Preparation for and attendance of the required trial team meetings or submission meetings Preparation, conduct, and documentation of kick-off meetings, e.g. for TDO/CTP, IB or CTR writing Preparation, conduct, and documentation of Results Alignment Meetings (RAM; not applicable for Phase I in healthy volunteer studies) Writing of drafts including appropriate in-text tables and figures according to the timelines agreed upon with trial/project team Provision of drafts and management of all review cycles by the trial/project team, reaching consensus on comments/changes, integration of changes into the text, and completion of the Review Documentation Form (as applicable) Initiation and monitoring or conducting of Quality Control (QC) checks as well as completion of the Quality Control Documentation Form (QCDF) Creation and provision of the final document version to the trial/project team Initiation of publishing and pre-archive checks, monitoring and resolution of findings E-approval of final clinical document in the EDMS Technical checks after the final draft of initial IBs and IB updates in the EDMS, and by going through a Final Formatting checklist document FTE Medical Writer will follow the appropriate process as per document type and according to sponsor SOPs Qualifications Bachelor’s degree in a scientific, clinical, regulatory, or related field required; advanced degree (e.g., MSc, PhD, PharmD, MD) preferred Approx 5 years of experience in medical writing within the biopharmaceutical, biotechnology, or CRO industry; equivalent experience in clinical or preclinical development will also be considered Strong knowledge of global regulatory requirements and guidelines (e.g., ICH, FDA, EMA) across all phases of clinical development Broad understanding of clinical research processes, including study design, data analysis, and regulatory submission requirements Demonstrated ability to lead writing activities for complex documents and provide strategic input to cross-functional teams Excellent written and verbal communication skills, with the ability to clearly and accurately present complex scientific and clinical information Strong organizational, time management, and project management skills, with the ability to manage multiple priorities and meet tight deadlines Proven ability to work collaboratively in a cross-functional, team-oriented environment while also operating independently when needed High attention to detail with a commitment to quality, consistency, and scientific accuracy Proficiency in Microsoft Word and document formatting best practices Experience with electronic document management systems (eDMS) and familiarity with document templates, style guides, and structured authoring tools 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. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. EEO Minorities/Females/Protected Veterans/Disabled #J-18808-Ljbffr