Co jobs in Madrid - Page 19Create job alerts

Busco cofundador CTO Líderorientado a ventas B2B partnerships y gotomarket que multiplique la tracción comercial Busco un cofounder orientado a.

Residencia en Galicia Responsabilidades Planificación y gestión integral de proyectos de desarrollo de software, desde la fase inicial hasta la entrega final. Qué ofrecemos? Contrato Indefinido en una compañía 100% digital tecnológica Flexibilidad horaria y opción de teletrabajo Formación co

Empresa perteneciente a Grupo Delso, líder en el sector de los fertilizantes busca incorporar a su equipo un/a: RESPONSABLE DE CONTABILIDAD (CON FRANCÉS) Esta es tu oportunidad para unirte a una empresa en crecimiento que gestiona un negocio clave en el mercado marroquí. Desarrollo profesional co

Comunicación, las Artes y la Inteligencia Artificial , y te entusiasma transformar la enseñanza superior, quizá esta oportunidad sea para ti. Profesionales con un Doctorado finalizado en Comunicación, Artes o áreas afines. Responsable Transversal de Innovación y Desarrollo en la Facultad de Co

Buscamos una persona proactiva, con capacidad de planificación, organizada y resolutiva, capaz de trabajar en equipo en un entorno de colaboración, flexible y con habilidades de comunicación (tanto verbal como escrita), y con interés y visión de mejora continua. En ENAC estamos comprometidos co

QUIERES FORMAR PARTE DE GDC BEAUTY GROUP? Somos un innovador grupo global de belleza que opera con diferentes marcas en el sector de la cosmética profesional desde hace más de 60 años. GdC Beauty Group nace tras el inicio de un plan estratégico de crecimiento sostenible con un claro objetivo: co

This role involves executing go-to-market strategies for Spain and France, building acquisition channels, and driving B2B sales for small firms while effectively scaling B2C operations.

Y por ello necesitamos incorporar un/a Técnico/a de Ejecución de Obra (DEO) para nuestro equipo actual en Madrid.El Grupo IDP (IDP, Indutec, Ecointegral, IDP Data Center, Ibertel), perteneciente a Bureau Veritas , es el primer grupo de servicios de ingeniería especialista BIM en España, co

Precisamos incorporar un/a trabajador/a social en nuestro centro situado en Vicálvaro-El Cañaveral (Madrid) /ppbr/ppRealizará las siguientes funciones: /ppbRealizar y coordinar con Dirección la planificación y ejecución de las acciones comerciales, /b /ppbestableciendo contacto y relación co

Position Overview We are seeking an exceptional Clubhouse Manager to lead and elevate all clubhouse operations, with a strong focus on Food & Beverage excellence. Experiencia demostrada en un puesto senior en casa club, hospitalidad o liderazgo en F& B (preferiblemente en entorno de lujo) Sólido co

Como Director/a de Canal y Alianzas Mid-Market, tendrás que: Implementar la estrategia de Canal y Alianzas incluyendo el Partners Program que incluye los programas de incentivos, certificaciones, soporte, co-marketing, etc. Liderar y dinamizar la estrategia de canal y alianzas para el segmento Mid-

Dominio de español e inglés nivel intermedio (obligatorio). En Brach Madrid, estamos buscando una persona que quiera realizar sus prácticas en Recepción de Spa Wellness, La Capsule. Si eres una persona organizada con ganas de aprender y desarrollarte en un entorno dinámico, ¡Nos encantaría co

Responder proactivamente ante la diagnosis de averías y reparaciones con el objetivo de conseguir una solución. Llevar a cabo las reparaciones asignadas para lograr un funcionamiento continuo.

Por favor, asegúrese de leer atentamente los siguientes detalles antes de enviar cualquier solicitud.Buscamos un/a nuevo/a dependiente/a para incorporarse al actual equipo.Persona con clara orientación comercial, pasión por la venta personalizada, que quiera aprender y crecer profesionalmente, co

To Apply Please send your CV to Subject line: Administrative Assistant Application. Administrative Assistant & Bookkeeper. Manage accounts payable and accounts receivable processes Process invoices and maintain accurate bookkeeping records Assist with bank reconciliations and expense tracking Suppor

Native or professional fluency in English is required; proficiency in a second European language (e. Lead the end‑to‑end process of establishing new legal entities in Europe, including tax registration, bank account openings, and the recruitment of local finance teams. Deep understanding of Euro

Buscamos incorporar a nuestro equipo una persona curiosa, analítica y con buena capacidad de conversación profesional para identificar y documentar proyectos de construcción en el mercado español.Aunque la experiencia profesional y las cualificaciones son clave para este puesto, asegúrese de co

En Ontime, empresa líder en operaciones logísticas integrales en Iberia, promovemos una política de contratación inclusiva y justa para todos. Colectivo Ontime con Banco Santander : disfruta de múltiples ventajas y servicios pensados especialmente para ti. Acceso al programa “Soy Ontime” co

Buscamos Técnicos/as de calidad y medio ambiente para integrarse en las estructuras de los proyectos, con el fin de garantizar una gestión eficiente de los sistemas de gestión y cumplimiento de la normativa aplicable, y su correcta aplicación e integración en los proyectos. Titulado superior co

At The Knot Worldwide, we champion celebration - and that starts with celebrating our people.Our employees are passionate dreamers, thoughtful doers, and lifelong learners who power meaningful moments for millions around the world.We’re united by authentic connection, shared purpose, and a deep co

At The Knot Worldwide, we champion celebration - and that starts with celebrating our people.Our employees are passionate dreamers, thoughtful doers, and lifelong learners who power meaningful moments for millions around the world.We’re united by authentic connection, shared purpose, and a deep co

Buscamos un / a Consultor SAP CO Senior para integrarse al área de Procesos de un cliente de referencia mundial en el sector farmacéutico, aportando su expertise técnico y operativo en la gestión financiera.Tiene las cualificaciones y habilidades adecuadas para este trabajo? Descúbralo a contin

Ready to innovate the packaging of tomorrow? Hero R&D are strategic partners, passionate co-creators, and experienced problem solvers.

Una empresa emergente en Bilbao busca co-líderes para proyectos que desarrollen ideas de negocio exitosas.Se requiere mínimo 3 años de experiencia en roles similares, habilidades de liderazgo y capacidad de análisis.Ofrecen un 40/45% de participación en la start-up sin inversión inicial, adem�

Todo listo para enviar su solicitud? Asegúrese de comprender todas las responsabilidades y tareas asociadas a este puesto antes de continuar.Tigrane Seydoux : traer la calidez de las pequeñas trattorias italianas al mundo.Lo que comenzó como un único local en París es hoy un fenómeno global co

The ideal candidate will have over 5 years of experience in the tech/startup industry and a proven ability to turn ideas into successful businesses.

A leading startup accelerator is looking for an entrepreneurial CEO based in Barcelona to lead a venture focused on redefining menopause experiences. The role entails establishing vision, driving growth, and leading a motivated team. Ideal candidates have over 8 years in management, preferably in digital health and wellness sectors, and possess strong leadership and strategic skills. This permanent position offers a competitive salary and significant equity as co-founder, aiming to impact women's health positively. #J-18808-Ljbffr

Summary LOCATION: London or Barcelona ROLE TYPE: Hybrid Working The Global Medical Affairs Director develops and implements strategic and operational Therapeutic Areas (TAs) Global Medical Affairs programs. Focused on innovative evidence and launch readiness along with post-market solutions, including medical affairs planning and execution of the medical/scientific engagement strategy. They address and deliver strategic pre-launch and launch medical activities needs for patient, clinical, access and value to health care systems. Providing expertise in the development and execution of the overarching strategies and providing inputs during design and along the end-to-end execution of programs. They also develop and execute the Integrated Evidence Plan (IEP)/functional specific programs to maximize the value proposition for the prioritized launch portfolio and impact of our medicines. About The Role Key Responsibilities: The Global Medical Affairs (GMA) team acts as enterprise medical voice across the asset lifecycle and leads the medical strategy for the TA. They develop/own IEP and provide input into development while ensuring US and International medical perspective is reflected. Responsible for the implementation of medical strategies for early programs globally with focus on innovative evidence solutions including interventional studies, Non-interventional studies (NIS) and Real World Evidence (RWE) studies and implementation science projects. With extensive experience in drug development the Global Medical Affairs Director will be able to lead Integrated Evidence Packages in situations with higher scientific complexity and potential regulatory challenges. They will also manage the most complex assets and those that potentially will require deeper pharmacovigilance expertise. Acting as a subject matter expert in the development of the overarching strategies, providing inputs during design and along the end-to-end execution of programs across different disease areas. They will provide leadership and deep medical expertise in the TA, pivoting support based on business priorities and will represent GMA with senior stakeholders. Major Accountabilities Lead development and execution of medical affairs strategy for TA/Asset priority programs including transformative tactics such as: research/population health, innovative partnerships and integrated evidence plans Co-develop plans for evidence generation, Medical Science Liaison (MSL) / Field Medical Affairs strategy, innovative medical education programs and scientific communications plans for external stakeholders, scientific publication planning and Medical Expert network development with TAs Financial tracking to ensure timely and cost-effective development & execution of medical activities Prepare Safety Review Committee (SRC) submissions for TA assets within remit Partner with Development, S&G, US and International cross-functions to shape portfolio early and diversify evidence to achieve broad access at launch and to enhance impact on clinical practice for priority programs Represent GMA around prioritized portfolio with internal and external audiences, in collaboration with TAs including the investment, medical and regulatory communities, as well as pharmaceutical or biotechnology industry collaborators/partners Provide direction and input into the development and implementation of successful reimbursement and market-access strategies Provide proactive input to Development on potential new therapeutic indications, to enrich Registration Programs and to consider new therapeutic opportunities. Ensure GMA activities are designed and executed in compliance with company policy guidelines and highest medical quality standards and that Patient Access programs are supported for all brands within the GMA and delivered with full compliance Essential Requirements Medical Degree (MD) (Preferred) or PhD/PharmD in Health Sciences. Specialist Degree or specialist qualification related to cardiovascular medicine (including anticoagulation) and/or pharmaceutical medicine (or its equivalent) is an advantage. 5+ years in Pharmaceutical Industry with experience in Medical Affairs at global level and/or Clinical Development Deep understanding of health care systems and key external stakeholders Critical thinker, agile mindset, ability to navigate uncertainty without major supervision, ability to truly collaborate across functions and markets (serve-partner-co-create) and a strong track record of delivery focus for time and quality in medical affairs projects Successful development and implementation of innovative programs and processes Understands unmet medical needs, generates the right evidence to fulfil them, uses innovative, multichannel communication formats for effective evidence dissemination Credibility as peer expert with external stakeholders; Patient interaction and engagement experience. Firm working knowledge of Good Clinical Practice (GCP,) scientific and clinical methodology, protocol designs, management and regulatory requirements for clinical studies designated for review by regulatory authorities. Preferred Experience Highly preferred: Cardiovascular medicine expertise including expertise with anti-coagulant therapy, significant medical affairs early asset lifecycle, pre-launch and launch experience in Global organizations Experience in developing and executing “Best in Class” processes at scale Clinical trial research experience conducted in a pharmaceutical or equivalent academic environment in cardiovascular medicine is strongly desired. Why Novartis Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: You’ll Receive You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. Commitment To Diversity And Inclusion Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve. Join Our Novartis Network If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? Benefits and Rewards Learn about all the ways we’ll help you thrive personally and professionally. Read our handbook (PDF 30 MB) #J-18808-Ljbffr

HealthTech Co-Founder & COO: Build a €1B+ Startup • Madrid, Spain A startup incubator is looking for ambitious entrepreneurs to build their own companies. The role includes receiving a salary or up to €500k in funding while developing the startup.

Si te apasiona el análisis de datos, la gestión de calidad de datos y la definición de procedimientos de gobierno, ¡te estamos buscando!. Inclusión y Diversidad Consideramos que la diversidad es enriquecedora y queremos velar por la inclusión e igualdad de oportunidades, por lo que contamos co

You will take full responsibility for your startup's growth, develop personal skills, and iterate your product towards market fit while being part of an elite community of founders and investors. A leading startup incubator is seeking a Longevity Co-Founder / Head of Product to build a €1B+ compan

A leading startup incubator in Spain is seeking ambitious entrepreneurs to own and scale their startups, particularly in Agentic AI.

Summary The Global Medical Affairs Director develops and implements strategic and operational TAs Global Medical Affairs programs, with a focus on innovative evidence and/or launch readiness and/or post-market solutions, including medical affairs planning and execution of the medical/scientific engagement strategy addressing and delivering strategic pre-launch and launch medical activities needs for patient, clinical, access and value to health care systems -Provides expertise in the development and execution of the overarching strategies, providing inputs during design and along the end-to-end execution of programs -Develops and executes the Integrated Evidence Plan (IEP)/functional specific programs to maximize the value proposition for the prioritized launch portfolio and impact of our medicines. Summary The Global Medical Affairs Director develops and implements strategic and operational TAs Global Medical Affairs programs, with a focus on innovative evidence and/or launch readiness and/or post-market solutions, including medical affairs planning and execution of the medical/scientific engagement strategy addressing and delivering strategic pre-launch and launch medical activities needs for patient, clinical, access and value to health care systems -Provides expertise in the development and execution of the overarching strategies, providing inputs during design and along the end-to-end execution of programs -Develops and executes the Integrated Evidence Plan (IEP)/functional specific programs to maximize the value proposition for the prioritized launch portfolio and impact of our medicines. About The Role LOCATION: London, Dublin, Barcelona. ROLE TYPE: Hybrid Working, The Global Medical Affairs Director develops and implements strategic and operational Therapeutic Areas (TAs) Global Medical Affairs programs. Focused on innovative evidence and launch readiness along with post-market solutions, including medical affairs planning and execution of the medical/scientific engagement strategy. They address and deliver strategic pre-launch and launch medical activities needs for patient, clinical, access and value to health care systems. Providing expertise in the development and execution of the overarching strategies and providing inputs during design and along the end-to-end execution of programs. They also develop and execute the Integrated Evidence Plan (IEP)/functional specific programs to maximize the value proposition for the prioritized launch portfolio and impact of our medicines. Major Accountabilities Lead medical–scientific input for Global Medical Affairs studies: evidence gap and competitor analyses; study planning, execution and reporting; authoring study documents (concepts, protocols, SAP/DAP, CRFs, reports, publications); advisory board and training materials; ongoing medical review and interpretation (Phase IIIB–IV, PMS, NIS, RWE); act as key medical contact. Serve as a disease-area medical and scientific expert for internal stakeholders (PMAT, GCT, ISRC, Research, Device, Marketing, Patient Access, Country Organisations) and external stakeholders (HCPs, PAGs). Co-develop Brand/Franchise Medical Affairs strategy and plan; shape programme/brand publication plans with Scientific Communications; provide medical leadership to new product and pipeline activities. Lead and support evidence generation across RWE and HEOR in collaboration with RWE/HEOR leaders and Country Medical teams. Provide medical input and support for education and communications: speaker training, medical expert engagement, pre-/launch activities; create and review scientific materials in partnership with Scientific Communications. Enable Global Field Medical Excellence: supply up-to-date content and training for MSLs and Country Medical Affairs; support implementation of key Field Medical processes and discuss outcomes to drive actions; develop content for digital tools. Provide medical input across programme deliverables: Medical Affairs sections of IDP/CDP; support regions/countries on local Medical Affairs clinical programmes and pre-launch; value dossiers and payer advisory participation; global guidance and NEETs; review publications; input to PSURs/DSURs. Ensure medical accuracy, compliance and approvals for promotional and non-promotional global materials; deputise for the Executive Medical Director across PMAT/GCT/GPT, regional alignment, internal decision boards and external activities. Essential Requirements Medical Degree (MD) Specialist Degree or specialist qualification related to Rheumatology. Pharmaceutical Industry with experience in Medical Affairs at global level and/or Clinical Development Firm working knowledge of Clinical Trials, including Good Clinical Practice (GCP,) scientific and clinical methodology, protocol designs, management and regulatory requirements for clinical studies designated for review by regulatory authorities Deep understanding of health care systems and key external stakeholders Critical thinker, agile mindset, ability to navigate uncertainty without major supervision, ability to truly collaborate across functions and markets (serve-partner-co-create) and a strong track record of delivery focus for time and quality in medical affairs projects Successful development and implementation of innovative programs and processes Understands unmet medical needs, generates the right evidence to fulfil them, uses innovative, multichannel communication formats for effective evidence dissemination Credibility as peer expert with external stakeholders; Patient interaction and engagement experience. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally. Read our handbook (PDF 30 MB) #J-18808-Ljbffr

Una empresa líder en elevación busca un JEFE DE VENTAS para el área Noroeste de España, incluyendo Galicia, Asturias y Castilla y León. Es fundamental el manejo de herramientas como MsOffice y conocimientos de PowerBI. La persona ideal tendrá formación en empresariales o ingeniería y experie

Regulatory Affairs & Pharmacovigilance Platforms,** you will play a pivotal role in spearheading the implementation and support of digital solutions and informatics systems to facilitate the efficient functioning and continuous enhancement of Medical, Regulatory and Pharmacovigilance operations. This position demands strong strategic leadership, team management, and close collaboration with various departments to optimize regulatory compliance and data management. In your capacity as the Digital Lead for Medical, Regulatory Affairs & Pharmacovigilance, you will serve as the key point of contact for business stakeholders in these areas, with the goal of maximizing the value derived from digital investments and technology partnerships. This role requires a comprehensive understanding of Medical, Regulatory Affairs and Pharmacovigilance regulatory frameworks and obligations. It is a highly integrated role, necessitating your ability to influence, negotiate, project plan, and oversee initiatives to drive alignment and performance across the organization. Success in this position hinges on your enthusiasm, keen attention to detail, and a deep commitment to advancing the quality and safety of all our platforms to benefit patients. You will provide strategic leadership, overseeing a dynamic team and collaborating with cross-functional departments to elevate our digital platforms and operations. Main responsibilities * Strategic Technology Liaison: Act as the pivotal link between the Global Science- Medical RA & PV functions, and technology providers, overseeing the delivery of digital solutions for Medical, RA & PV information. Establish and maintain strategic vendor relationships and governance structures.* Digital Strategy: Develop and execute a comprehensive digital strategy for Medical, RA and PV platforms, aligning with organizational goals and regulatory requirements.* Technical Solutions Leadership: Lead discussions on technical feasibility, prototype development, and the design of efficient, adaptable, and scalable technology solutions, all in adherence to company policies, regulatory standards, and integration goals.* Team Leadership: Build, mentor, and lead a high-performing team of digital experts (both internal & external) focused on Medical, RA and PV domains, fostering innovation and excellence.* Technology Roadmap Execution: Manage the execution of the approved technology roadmap, ensuring the delivery of development and validation artifacts to meet high-quality standards, compliance, and audit readiness.* Platform Enhancement: Drive the enhancement and optimization of digital platforms used in Medical Affairs, Regulatory Affairs and pharmacovigilance, ensuring efficiency and compliance.* Stakeholder Collaboration: Collaborate closely with Medical Affairs, Regulatory Affairs, PV, Digital, and other relevant departments to align digital initiatives and ensure seamless integration of digital solutions.* Application Support Management: Supervise both daily and scheduled support for Medical RA & PV platforms collaborating with managed support teams both internal and external eto resolve issues with the highest level of quality and stakeholder satisfaction.* Vendor Management: Oversee relationships with technology vendors and service providers, ensuring the delivery of high-quality solutions and services.* Data Insights: Leverage data analytics and insights to inform decision-making, optimize processes, and drive continuous improvement in Medical, RA and PV operation.* Regulatory Compliance: Ensure that relevant digital platforms and processes comply with all relevant regulatory requirements, maintaining the highest standards of quality and safety.* Budget Oversight: Manage the budget for digital initiatives within Medical, RA and PV, optimizing resources for maximum strategic impact.* Platform Compliance: Collaborate with relevant stakeholders to ensure that solutions, such as Global Safety Database- ARIS G- LifeSphere MultiVigilance (LSMV), Veeva RIMS and Medical Affairs Global HCP Events platform, are developed in line with the requirements of 21 CFR Part 11 and systems validation standards.About you Experience* Bachelor’s degree in a relevant field; Master’s degree preferred. Proven extensive experience in digital leadership roles within the Lifesciences or consumer healthcare industry.* Proven experience in overseeing and implementing digital systems like Medical Affairs event platforms, RIMS and publishing platforms and ARIS or similar PV Platforms to optimize adverse event monitoring, case processing, and regulatory compliance.* Strong understanding of Medical affairs, Regulatory Affairs and PV processes.* Exceptional leadership and team management skills.* Excellent communication and stakeholder engagement abilities.* Demonstrated ability in evaluating, negotiating, and managing contracts and Statements of Work with Medical, RA and PV technology vendors and implementation/support providers.* Possesses comprehensive knowledge of Quality Assurance and regulatory compliance, including 21 CFR Part 11 and FDA regulations, ensuring technology solutions meet industry standards.* Strong problem-solving capabilities and a track record of successful project delivery.* Languages: Advanced English required, Spanish or French preferredSoft skills* Strong communication skills* tion, negotiation, and interpersonal skills* Demonstrated conflict resolution & problem-solving skills in a global environment.* Strong appetite to learn and discover, entrepreneur mindset.* Adaptable and open to change* Team player, service-oriented* Analytical and synthetic, able to formalize solutions, good writing skills.* Strong oral and written communication skills* With leadership attitude, autonomy and results driven.* Role model our 4* values: teamwork, #J-18808-Ljbffr

A startup accelerator program in Madrid seeks ambitious entrepreneurs to build and scale their own startups. The program offers a salary during the startup development phase or potential funding up to €500k. Excellent English communication is essential for responsibility in growing your startup to

Among the portfolio of services, TCS has information technology services, asset-based solutions, global consulting, engineering and industrial services, digital solutions and services, application maintenance and development, quality assurance and testing services, IT infrastructure and BPS. Tata Co

Join to apply for the Planning Manager, EU Central Operations role at Amazon Continue with Google 20 hours ago Be among the first 25 applicants Description The goal of Amazon Logistics is to build a world class last mile delivery operation. Amazon aims to exceed the expectations of our customers by ensuring that their orders are delivered quickly, accurately, and in the most cost effective way possible. Central Operations (CO) is a strategic initiative within Amazon Logistics (AMZL) to develop scalable solutions for the increasingly complex last mile delivery network. It focuses on forecasting, route planning, demand scheduling, and last mile delivery. We seek an Operations Manager with a proven track record of operational excellence to lead scalability efforts, develop strong processes and culture, and operate effectively in high ambiguity environments. This role offers opportunities for strategic thinking, innovation, and collaboration across teams to scale Central Operations. Key job responsibilities Lead a team of Managers and Logistics Associates to optimize day-to-day operations and projects for EU CO, focusing on KPIs such as forecast accuracy and process adherence/improvement. Drive performance metrics, program scoping, rollout, compliance, and stakeholder engagement. Develop best practices and standard work for the network. Communicate proactively with various departments, maintain high service levels, and resolve issues impacting business continuity. Conduct strategic research into process improvements and make real-time decisions. Maintain and report accurate statistics, management reports, and analysis. Please submit your CV in English. Basic Qualifications Degree qualification or equivalent Experience with planning, standard work practices, and performance metrics Strong analytical and problem-solving skills Flexibility to work various hours including weekends and public holidays Intermediate Excel skills Experience leading teams Effective communication skills in English Organizational and time management skills Teamwork mentality and ability to build trustful relationships Preferred Qualifications Not required but advantageous: Advanced or master’s degree Experience with Lean, Kaizen, or Six Sigma methodologies Experience in supply chain, logistics, or operations Data analysis and report creation for leadership Knowledge of SQL, MS Office, Tableau, or Python Amazon values diversity and is an equal opportunity employer. For privacy and accommodation details, please refer to Amazon’s privacy notice and accommodations page. #J-18808-Ljbffr

Summary The Global Medical Affairs Director develops and implements strategic and operational TAs Global Medical Affairs programs, with a focus on innovative evidence and/or launch readiness and/or post‑market solutions, including medical affairs planning and execution of the medical/scientific engagement strategy addressing and delivering strategic pre‑launch and launch medical activities needs for patient, clinical, access and value to health care systems – Provides expertise in the development and execution of the overarching strategies, providing inputs during design and along the end‑to‑end execution of programs – Develops and executes the Integrated Evidence Plan (IEP)/functional specific programs to maximize the value proposition for the prioritized launch portfolio and impact of our medicines. About the Role LOCATION: London, Dublin, Barcelona. ROLE TYPE: Hybrid Working. The Global Medical Affairs Director develops and implements strategic and operational Therapeutic Areas (TAs) Global Medical Affairs programs. Focused on innovative evidence and launch readiness along with post‑market solutions, including medical affairs planning and execution of the medical/scientific engagement strategy. They address and deliver strategic pre‑launch and launch medical activities needs for patient, clinical, access and value to health care systems. Providing expertise in the development and execution of the overarching strategies and providing inputs during design and along the end‑to‑end execution of programs. They also develop and execute the Integrated Evidence Plan (IEP)/functional specific programs to maximize the value proposition for the prioritized launch portfolio and impact of our medicines. Major Accountabilities Lead medical‑scientific input for Global Medical Affairs studies: evidence gap and competitor analyses; study planning, execution and reporting; authoring study documents (concepts, protocols, SAP/DAP, CRFs, reports, publications); advisory board and training materials; ongoing medical review and interpretation (Phase III–IV, PMS, NIS, RWE); act as key medical contact. Serve as a disease‑area medical and scientific expert for internal stakeholders (PMAT, GCT, ISRC, Research, Device, Marketing, Patient Access, Country Organisations) and external stakeholders (HCPs, PAGs). Co‑develop Brand/Franchise Medical Affairs strategy and plan; shape programme/brand publication plans with Scientific Communications; provide medical leadership to new product and pipeline activities. Lead and support evidence generation across RWE and HEOR in collaboration with RWE/HEOR leaders and Country Medical teams. Provide medical input and support for education and communications: speaker training, medical expert engagement, pre‑/launch activities; create and review scientific materials in partnership with Scientific Communications. Enable Global Field Medical Excellence: supply up‑to‑date content and training for MSLs and Country Medical Affairs; support implementation of key Field Medical processes and discuss outcomes to drive actions; develop content for digital tools. Provide medical input across programme deliverables: Medical Affairs sections of IDP/CDP; support regions/countries on local Medical Affairs clinical programmes and pre‑launch; value dossiers and payer advisory participation; global guidance and NEETs; review publications; input to PSURs/DSURs. Ensure medical accuracy, compliance and approvals for promotional and non‑promotional global materials; deputise for the Executive Medical Director across PMAT/GCT/GPT, regional alignment, internal decision boards and external activities. Essential Requirements Medical Degree (MD) Specialist Degree or specialist qualification related to Rheumatology. Pharmaceutical Industry experience in Medical Affairs at global level and/or Clinical Development. Firm working knowledge of Clinical Trials, including Good Clinical Practice (GCP), scientific and clinical methodology, protocol designs, management and regulatory requirements for clinical studies designated for review by regulatory authorities. Deep understanding of health care systems and key external stakeholders. Critical thinker, agile mindset, ability to navigate uncertainty without major supervision, ability to truly collaborate across functions and markets (serve‑partner‑co‑create) and a strong track record of delivery focus for time and quality in medical affairs projects. Successful development and implementation of innovative programs and processes. Understands unmet medical needs, generates the right evidence to fulfil them, uses innovative, multichannel communication formats for effective evidence dissemination. Credibility as peer expert with external stakeholders; Patient interaction and engagement experience. Why Novartis Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? Benefits and Rewards Learn about all the ways we’ll help you thrive personally and professionally. Read our handbook (PDF 30 MB) #J-18808-Ljbffr

Buscamos teleoperadores/as para campaña de ONG!.Sea uno de los primeros solicitantes, lea la descripción completa del puesto a continuación y luego envíe su candidatura para que sea considerada.Si tienes experiencia en ventas telefónicas o call center y te apetece formar parte de un proyecto co

A consulting firm is seeking a Head of Finance (Europe) to lead financial strategy for expanding European operations. Responsibilities include establishing new entities, overseeing financial management, and ensuring compliance with local regulations. The ideal candidate has over 5 years of senior experience in finance, preferably in a trading environment, and holds relevant finance qualifications. Proficiency in English and a second European language is preferred. This role is pivotal in navigating the complexities of an early-stage international rollout. #J-18808-Ljbffr

Una empresa líder en retail busca un/a Head of Property para dirigir su estrategia de crecimiento en España.Este puesto implica controlar la expansión de la compañía identificando nuevas oportunidades y gestionando proyectos de construcción.Todas las responsabilidades incluyen supervisar la co

Responsable de Selección | Talent Acquisition Specialist | Conecto profesionales con oportunidades en los sectores industrial y tecnológico. Disponibilidad para viajar a nivel internacional de forma ocasional. La persona seleccionada se encargará de recopilar y analizar información técnica y co

Buscamos un/a bIngeniero/a en Electrónica Industrial y Automática /b para garantizar el análisis, coordinación, implementación y supervisión de las soluciones TICS definidas en los pliegos y contratos, trabajando estrechamente con los equipos internos (IT, Estudios, Compras, Delegaciones) y co

Quiénes somos? Occident es uno de los líderes del sector asegurador español, y del seguro de crédito Con un crecimiento constante y una gran implantación, cuenta con más de 7.A partir de enero 2024 Seguros Catalana Occidente, Plus Ultra Seguros y Seguros Bilbao se han fusionado y somos.Para co

Una empresa líder en el sector de comida rápida busca un responsable de unidad de negocio para gestionar cuentas de explotación y supervisar el funcionamiento diario del restaurante. Se requiere experiencia previa de 2 años y habilidades en liderazgo y gestión de equipos. El puesto ofrece un co

Una agencia gubernamental de vivienda en Córdoba busca un Técnico Medio Económico-Financiero.Se requiere tener relación laboral con la agencia, un título universitario y disponibilidad para viajar.Este puesto es para una promoción interna, y el candidato debe cumplir con ciertos requisitos, co

Una consultora de empleo en Coslada busca un/a Gerente de Oficina para liderar su equipo de gestión fiscal, laboral y mercantil. Se requiere un/a profesional con más de 4 años de experiencia en la ocupación, carnet de conducir y titulación en Económicas, Empresariales o afines. Se ofrece un co