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Job Description: An opportunity for an Occupational Health Physician has arisen within Airbus Defence and Space in Getafe (Madrid). The selected candidate will join the Medical & Occupational Health Team. Our mission is to safeguard the health, safety, and well-being of all Airbus employees. As part of our multidisciplinary health unit, you will play a proactive role in preventive medicine, emergency response, and promoting a culture of health across our Getafe site. Responsibilities Your main tasks and responsibilities will be: Perform comprehensive medical surveillance tailored to specific job profiles and risk exposure to effectively prevent, diagnose work-related pathologies, and facilitate job retention. Identify, assess, and refer vulnerable employee groups or individuals to relevant specialists when appropriate. Propose, pilot, and participate in occupational health actions and projects in close cooperation and consultation with specialized teams. Propose fitness-to-work recommendations based on workplace risks and individual health assessments. Support and deliver* the organization of emergency responses and high-quality first-aid provisions on-site. Skills & Experience Is your profile aligned with the following criteria? If so, apply now! We are looking forward to meeting you: Education: University Degree in Medicine (specialization in Occupational Medicine / Medicina del Trabajo is highly valued). Experience: At least 2-3 years of experience in a related occupational health position. Languages: Advanced/Negotiation level in both English and Spanish is mandatory. Soft Skills: Excellent communication skills, strong empathy, and a proactive, hands-on approach to problem-solving. What’s In It For You? (Airbus Benefits) At Airbus, we are fully focused on our employees and their well-being. By joining our team in Getafe, you will enjoy a comprehensive benefits package: Work-Life Balance: Generous annual vacation days plus additional days off throughout the year. Financial Peace of Mind: Competitive salary, life & health insurance, employee stock options, and a structured retirement plan. Growth & Development: Excellent upskilling opportunities, access to study grants, and great career prospects in a truly global environment. Easy Commuting: Collective transport service (subject to calendar and home location). Top-tier On-site Facilities: Free canteen, on-site kindergarten, and a dedicated medical office. Purpose-Driven Culture: Opportunities to collaborate in various social and Corporate Social Responsibility (CSR) initiatives. * Perks & Discounts: Exclusive access to special rates on products and partner benefits. This job requires an awareness of any potential compliance risks and a commitment to act with integrity, as the foundation for the Company’s success, reputation and sustainable growth. Company: Airbus Defence and Space SAU Employment Type: Permanent ------- Experience Level: Professional Job Family: Health & Safety By submitting your CV or application you are consenting to Airbus using and storing information about you for monitoring purposes relating to your application or future employment. This information will only be used by Airbus. Airbus is committed to achieving workforce diversity and creating an inclusive working environment. We welcome all applications irrespective of social and cultural background, age, gender, disability, sexual orientation or religious belief. Airbus is, and always has been, committed to equal opportunities for all. As such, we will never ask for any type of monetary exchange in the frame of a recruitment process. Any impersonation of Airbus to do so should be reported to emsom@airbus.com . At Airbus, we support you to work, connect and collaborate more easily and flexibly. Wherever possible, we foster flexible working arrangements to stimulate innovative thinking.

OutSystems Tech Lead (Remote from Spain) We are still looking for the very Top Talent and we would be delighted if you were to join our team! More in details, UST is a multinational company based in North America, certified as a Top Employer and Great Place to Work company with over 35,000 employ

Arquitecto/a Software Tech Lead Java Descripción ¡Únete a Zemsania como Arquitecto/a Software - Tech Lead Java! En Zemsania, buscamos un/a Arquitecto/a Software con enfoque en Liderazgo Técnico Java para unirse a nuestro equipo en Madrid.Si tienes una pasión por la tecnología, una sólida

Tech Lead AI Conversational Agents Tech Lead AI Conversational Agents Country: Spain COMIENZA AQUÍ Santander (www.Juntos, estamos impulsando una transformación centrada en el cliente que valora el pensamiento audaz, la innovación y el coraje para desafiar lo que es posible.Esto es más q

Tech Lead | Java & Microservicios ¡Seguimos buscando talento y nos encantaría que te unieras a nuestro equipo! Para que nos conozcas algo mejor, UST es una multinacional norteamericana certificada como Top Employer y Great Place to Work con más de 35.Somos líderes en servicios de tecnología

Preferiría alguien con experiencia en acompañamiento a pacientes y buena comunicación. El acompañante debe ser puntual, respetuoso y capaz de ayudar en situaciones simples si surgen, además de mantener la confidencialidad de mi información médica. Estoy buscando a alguien de confianza para ac

Idealmente alguien que hable español, con paciencia, discreción y experiencia en acompañamiento a personas mayores o con movilidad reducida. Busco a alguien de confianza para acompañarme a una cita médica en Madrid. La persona debe estar disponible para la cita programada, ayudarme a entender l

Estoy buscando a alguien de confianza para acompañarme a mis citas médicas.Vivo en España y necesito apoyo para traslados, gestionar papeles, y asegurar que llegue a tiempo a las consultas.La persona debe ser amable, paciente y capaz de comunicarse claramente en español.Preferiría un acompañan

Idealmente alguien puntual, con experiencia en asistencia sanitaria básica y buena comunicación. Soy adulto mayor y necesito apoyo para transporte, gestionar documentos y comprender las indicaciones del médico. Preferiría alguien que hable español y tenga seguro de responsabilidad.

Busco una persona de confianza para acompañarme a una cita médica en Granada.Soy adulto mayor y necesitaría apoyo para trasladarme al consultorio, gestionar trámites en la recepción y asegurar que entiendo las indicaciones del profesional.La cita es a mediodía, y me gustaría que la persona pu

Busco una persona de confianza para acompañarme a una cita médica en el centro de salud.Necesito apoyo para transporte, ayudar a recordar preguntas y tomar notas sobre el tratamiento recomendado.La cita es en un horario de mañana y preferiría una persona que hable español y tenga experiencia cu

Busco una persona de confianza para acompañar a una persona mayor a sus citas médicas en la ciudad.La tarea incluye transporte desde casa, inscribirse en la consulta, asistir a consultas y tomar notas básicas sobre indicaciones médicas.Se valoran amabilidad, paciencia y buena comunicación en es

Buscamos recepcionista para Centro Médico Cea Bermúdez en Madrid capital.

Descripción del puesto En el puesto de Auxiliar de clínica dental en PerioCentrum Madrid apoyarás al equipo odontológico en la atención integral de los pacientes y en la gestión diaria de la clínica. Requisitos * Experiencia previa como Auxiliar de Clínica Dental. Valorable formación como A

ROVI Pharma Industrial Services busca un profesional para participar en proyectos de ingeniería, desde el diseño hasta la ejecución en su planta de San Sebastián de los Reyes. La posición implica colaboración con diferentes departamentos y la documentación necesaria según las Buenas Práctic

Tech Lead AI Conversational Agents Tech Lead AI Conversational Agents Country: Spain COMIENZA AQUÍ Santander (www.Juntos, estamos impulsando una transformación centrada en el cliente que valora el pensamiento audaz, la innovación y el coraje para desafiar lo que es posible.Esto es más que un cam

Arquitecto/a Software Tech Lead Java Descripción ¡Únete a Zemsania como Arquitecto/a Software - Tech Lead Java! En Zemsania, buscamos un/a Arquitecto/a Software con enfoque en Liderazgo Técnico Java para unirse a nuestro equipo en Madrid. Tu Rol y Responsabilidades: Arquitecto Técnico con vocac

For our subsidiary Pacura med GmbH we are currently recruiting for new team members for the Austrian market.Pacura med GmbH is a German personnel service provider specialised in the medical sector.We are represented with a total of nine locations in Germany, Austria, Switzerland, and Norway.As part

Contar con certificado de discapacidad emitido por la Seguridad Social española o documento acreditativo válido en España (igual o superior al 33%).

Máster en Análisis de Datos Masivos (Big Data) para los Negocios. Impartir la asignatura Plataformas de Datos dentro del Máster en Análisis de Datos Masivos (Big Data) para los negocios.

Ecix Group busca a un profesional freelance con título homologado en España y al menos 3/4 años de experiencia en spa, preferiblemente en hoteles de lujo.Se valorará nivel de inglés C1.El trabajo implica saludar a los invitados, realizar tratamientos de belleza y mantener la limpieza del spa.Se

Únete a una farmacia donde tu trabajo marca la diferencia! En Farmacias Trébol buscamos un/a Farmacéutico/a Adjunto/a para incorporarse a nuestro equipo de Usera (Madrid).Si buscas un proyecto estable, jornada completa, un equipo cercano y la oportunidad de seguir desarrollándote profesionalment

Con un equipo de profesionales que supera las 9.España, trabajamos a través de una red de más de 200 centros en los que priman nuestros valores hospitalarios centrados en el cuidado y atención a la persona, y donde el trato humano y nuestra sensibilidad por cada una de ellas son la clave de lo q

IRIUM busca un/a Data Engineer con 3–5 años de experiencia para realizar tareas de soporte y mantenimiento de puestos de trabajo, garantizando el correcto funcionamiento de los equipos informáticos y la atención de incidencias de primer nivel.La información a continuación detalla los requisit

Talan Group is seeking a Senior Product Owner / Proxy PO in Málaga, Spain. This position focuses on Client Contribution and Client P&L solutions within an international banking technology team. The successful candidate will have strong experience in technology teams, managing project delivery, and translating complex functional needs into actionable tasks. This role also offers opportunities for training, career development, and benefits, including private medical insurance and flexible working arrangements. #J-18808-Ljbffr

SlashMobility busca un Desarrollador Java para colaborar con un cliente en el sector bancario. El candidato ideal diseñará y mantendrá módulos de software, garantizando el cumplimiento de las mejores prácticas de ingeniería. Las funciones incluyen participar en revisiones de código, realizar pruebas de integración y servir de mentor a ingenieros junior. Se requiere experiencia en desarrollo de software y una mentalidad proactiva para mejorar continuamente los servicios. #J-18808-Ljbffr

Airbus Defence and Space in Madrid is seeking an Occupational Health Physician to join their Medical & Occupational Health Team. You will play a key role in safeguarding the health and well-being of all Airbus employees through preventive medicine and emergency response. Ideal candidates hold a University Degree in Medicine, have 2-3 years of experience in occupational health, and are bilingual in English and Spanish. The role includes comprehensive benefits such as generous vacation days and professional growth opportunities. #J-18808-Ljbffr

LU-VE IBERICA S.L.U., filial de LU-VE SPA, busca un Ingeniero de Aplicaciones para apoyar al departamento técnico‑ventas en la Península Ibérica. Realizará ofertas técnico‑económicas, cálculo y selección de equipos, e interpretación de especificaciones y planos. Se requiere 1–3 años de experiencia, ingeniería o formación técnica, inglés fluido y conocimiento de SAP; se valora italiano. Ofrecemos desarrollo profesional en un entorno internacional y un salario competitivo según experiencia. #J-18808-Ljbffr

Syneos Health is seeking a skilled Biostatistician in Barcelona, Spain, to lead statistical projects across multiple studies. The successful candidate will serve as the primary contact for all biostatistics activities and provide consultancy on study design and protocol development. Responsibilities include creating Statistical Analysis Plans, mentoring team members, and ensuring high-quality data management. The role may involve minimal travel and requires a strong background in statistical analysis and programming, particularly with SAS. #J-18808-Ljbffr

SD Worx is seeking a FinOps Tech Lead to steer cloud financial management strategy, cost efficiency, and governance across multi-cloud environments. You will partner with engineering, finance, and product teams to drive data-driven decisions and automation. The role involves defining cost models, building real-time cost insights, and mentoring engineers in FinOps best practices while ensuring alignment with business goals and budget planning. #J-18808-Ljbffr

A digital travel company is seeking a Software Engineer to join their agile team. You will take ownership of product quality and collaborate with stakeholders to deliver innovative solutions. Ideal candidates have strong programming skills, preferably in JVM languages, and are passionate about applying AI technology. This role promises a flexible work schedule in a multicultural environment with opportunities for personal and professional growth. #J-18808-Ljbffr

Alexion Pharma Spain S.L. is seeking a Medical Director, Clinical Development in Hematology based in Barcelona. You will lead or support clinical development plans, represent Clinical Development on global teams, and drive the preparation of regulatory and publication documents for hematology programs. Requirements include an MD with hematology expertise, 3+ years in industry, and experience as a medical monitor for trials. #J-18808-Ljbffr

UST busca un Technical Lead Software Engineer con más de 5 años de experiencia en Java y microservicios, y con experiencia en AWS. El puesto es 100% remoto para un cliente del sector bancario, con sede en Madrid para referencia de idioma y cultura. Responsabilidades: liderar equipos, definir estándares de desarrollo, diseñar soluciones basadas en microservicios y garantizar la calidad de APIs REST, pruebas y migraciones a la nube. Se valora la mentoría y la gestión técnica. #J-18808-Ljbffr

QSalud, centro médico enfocado en consultas online, busca psiquiatras para un entorno de trabajo flexible y compatible con su práctica habitual. Las funciones incluyen evaluación y seguimiento por videoconferencia o teléfono, con colaboración presencial ocasional en Cuenca. Se ofrece colaboración mercantil (autónomo), flexibilidad de agenda y condiciones económicas competitivas por actividad presencial. #J-18808-Ljbffr

Pertenecemos al Grupo Quirónsalud, el grupo sanitario más importante de Europa.Dentro de la multinacional, en Q-Ready nos ocupamos de la gestión integral de la salud en las empresas, con más de 35 años de experiencia, somos referentes en la gestión de la incapacidad temporal en España, presta

Tamarind Intelligence, líder global en farmacéutica y cosmética, busca un Tech Lead Backend Node.js para guiar la transformación tecnológica y definir la arquitectura futura. El rol exige visión de negocio y capacidad de liderazgo en un entorno híbrido en Barcelona. Se valoran más de 5 años de experiencia en Node.js, AWS y diseño de APIs seguras, con foco en rendimiento. Ofrecemos onboarding, formación continua y horarios flexibles para un reto ambicioso. #J-18808-Ljbffr

Description POSITION DESCRIPTION Job Title: Critical Care Registered Nurse Supervised by: Charge Nurse/Nurse Manager Job Summary: Provides direct and indirect patient care in the critical care setting. Communicates with physicians about changes in patient’s clinical condition including hemodynamic monitoring, results of diagnostic studies and symptomatology. Is able to respond quickly and accurately to changes in condition or response to treatment. Additionally, is able to perform general nursing duties in all departments with adequate supervision. Participates in performance improvement and CQI activities. Demonstrates Competency in the Following Areas: Knowledge of medications and their correct administration based on age of the patient and their clinical condition. Follows the seven (7) medication rights and reduces the potential for medication errors. Ability to monitor hemodynamic status of patient and correctly interpret the results. Ability to perform a head-to-toe assessment on all patients and reassessments as per policy. This includes neonate, pediatric, geriatric and the general patient population. Ability to adequately assess and reassess pain. Utilizes appropriate pain management techniques. Educates the patient and family regarding pain management. Ability to interpret results of waived tests; take appropriate action on waived tests results. Performs all aspects of patient care in an environment that optimizes patient safety and reduces the likelihood of medical/health care errors. Supports and maintains a culture of safety and quality. Ability to formulate an individualized plan of care, revise plan as indicated by the patient’s response to treatment and evaluate overall plan daily for effectiveness. Formulates a teaching plan based upon identified learning needs and evaluates effectiveness of learning, family is included in teaching as appropriate. Demonstrates knowledge of cardiac monitoring, identifies dysrhythmias and treats appropriately based upon ACLS protocol. Provides care to patients with compromised nutritional/metabolic status. Provides care to patients requiring extensive fluid and electrolyte management. Communicates appropriately and clearly to charge nurse, co-workers and physicians. Consults other departments as appropriate to provide for an interdisciplinary approach to the patient’s needs. Provides care appropriate to disease condition and age of the patient. Coordinates and supervises patient care as necessary. Demonstrates an ability to assist physicians with procedures both in the Critical Care Unit and other departments. Demonstrates an ability to be flexible, organized and function well under stressful situations. Treats patients and their families with respect and dignity. Identifies and addresses psychosocial, cultural, ethnic and religious/spiritual needs of patients and their families. Functions as a liaison between administration, patients, physicians and other healthcare providers. Demonstrates knowledge of the principles of growth and development over the life span and the skills necessary to provide age appropriate care to the patient population served. Able to interpret data about the patient’s status in order to identify each patient’s age specific needs and provide care needed by the patient group. Interacts professionally with patient/family and involves patient/family in the formation of the plan of care. Maintains a good working relationship both within the department and with other departments. Documentation meets current standards and policies. Ability to assess and care for patients in the post anesthesia period both in the PACU and Critical Care. Participates in performance improvement activities. Professional Requirements: Adheres to dress code, appearance is neat and clean. Completes annual education requirements. Maintains regulatory requirements, including all federal, state, local regulations and accrediting organization standards. Maintains patient confidentiality at all times. Reports to work on time and as scheduled, completes work within designated time. Wears identification while on duty, uses computerized punch time system correctly. Completes inservices and returns in a timely fashion. Attends annual review and department inservices, as scheduled. Attends at least 12 staff meetings annually, or reads and returns all staff meeting minutes. Represents the organization in a positive and professional manner. Actively participates in performance improvement and continuous quality improvement (CQI) activities. Complies with all organizational policies regarding ethical business practices. Regulatory Requirements: · Graduate of an accredited school of nursing. · Current state Registered Nurse Licensure. · Current ACLS and BLS certification, prior to completion of department orientation. · One (1) year of RN experience, preferred. Language Skills: · Able to communicate effectively in English, both verbally and in writing. · Additional languages preferred. Skills: · Basic computer knowledge. Physical Demands: · Mobility, sight, hearing, verbal communication, changes in temperature, exposure to disagreeable elements, exposure to biological, mechanical, electrical, and chemical hazards. Frequent standing and walking. Lift up to 100 pounds. Carrying up to 40 pounds. Pushing/pulling up to 450 pounds. · This position is a safety sensitive position pursuant to Amendment 98 to the Arkansas Constitution § 2(25). A safety sensitive position means any position in which a person performing the position while under the influence of marijuana may constitute a threat to health or safety. This position is therefore “safety sensitive” due to the fact it requires the following: performing life-threatening procedures; working with hazardous or flammable materials, controlled substances, food, or medicine; and a lapse of attention while working in this position could result in injury, illness, or death. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the position without compromising patient care. #J-18808-Ljbffr

Nalco Water, An Ecolab Company, is looking for a Director of Marketing to lead their Europe High-Tech division focused on data center and microelectronics segments. This strategic role encompasses defining growth strategies, commercialization, and team development while working closely with various stakeholders to drive engagement and profitability. The ideal candidate will have extensive experience in marketing strategy within technical sectors, a strong background in team leadership, and excellent communication skills. A bachelor's degree in engineering and an MBA are preferred. #J-18808-Ljbffr

Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management. Responsibilities Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy Compile and maintain project-specific status reports within the clinical trial management system Interact with the internal project team, Sponsor, study sites, and third-party vendors Manage and perform quality control of our internal regulatory filing system Provide oversight and management of study supplies Create and maintain project timelines Coordinate project meetings and produce quality minutes Qualifications PhD in Life Sciences Fluency in English with solid presentation skills Ability to work in a fast-paced dynamic industry within an international team Prior experience within the CRO or pharmaceutical industry not required but will be advantageous Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives Awards Recognized by Forbes as one of America’s Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What To Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. #J-18808-Ljbffr

Infatica.io is seeking a Platform Architect & Tech Lead to own the Web Data Platform's technical architecture and guide engineering decisions. You will lead browser automation, data collection infrastructure, and large-scale distributed services while mentoring engineers and shaping technical strategy. You will collaborate with Product, Infrastructure, and Platform teams to ensure scalability, reliability, and growth, balancing long-term architecture with hands-on leadership. #J-18808-Ljbffr

The Patient Centered Solutions team (PCS) The PCS team leads the industry in the science of measuring the patient experience. We pair strategic consulting expertise with technical scientific knowledge to design and execute scientifically rigorous research that incorporates the patient voice into the development and commercialization of new medicines. This research includes qualitative (e.g., patient interviews, focus groups), quantitative (e.g., clinical outcome assessments (COAs)/patient‑reported outcomes (PROs), preference research) and passive (e.g., digital health technology tools) approaches to understand patient, caregiver and physician experiences and expectations of disease and treatment. Why join? Become part of a recognized global leader in patient‑focused research Keep growing with an organization that encourages and invests in continuous professional and personal development Develop your business and leadership skills further, with coaching from senior leaders Continue challenging yourself by addressing the toughest client issues, working across multiple geographies and solutions in a dynamic and crucial field for the industry Make a difference to patients by enabling the successful approval or launch of new treatments with features that are truly patient‑centric Responsibilities As a Manager, you will be responsible for overseeing a portfolio of projects in the field of patient‑centred research, and for developing and communicating strategic insights and recommendations to clients. In your day‑to‑day role, you will collaborate directly with IQVIA’s senior leaders and independently manage client relationships on each project. You will typically oversee 3‑6 projects at the same time. Your role will include: Acting as the day‑to‑day manager for a portfolio of consulting projects with responsibility for project delivery and client relationships Coaching and directing junior team members Developing a broad knowledge of patient science and how it addresses client needs for evidence generation and dissemination, regulatory and market access strategy Partnering with scientific team members to develop study material and conduct patient‑centered research Integrating results from research and analysis workstreams into strategic recommendations Creating reports, presentations and facilitating workshops Contributing to business development and assisting with or leading proposal development Supporting people‑related activities such as recruitment, training and development Leading special initiatives such as knowledge management and process improvement Mentoring 1‑3 junior team members Essential experience, skills and education required An advanced academic science degree in public health, epidemiology, psychology, sociology, medical anthropology, health economics or another related field Minimum of 5 years of experience in at least one of the above fields Previous experience in strategic consulting and project management Previous exposure to COA/PRO, patient preference and/or real‑world evidence methods Advanced knowledge of the healthcare regulatory processes and international payer systems Excellent written and verbal communication skills including presenting, facilitating meetings and workshops, and report writing Demonstrable analytical, interpretative, and problem‑solving skills Excellent interpersonal skills and ability to work effectively with others Ability to work in a fast‑paced environment with demonstrated ability to effectively manage multiple tasks Ability to establish and maintain effective working relationships in multi‑disciplinary and international teams Please submit your CV in English. #J-18808-Ljbffr

TD SYNNEX está buscando un Business Development Executive para Alcobendas, Madrid, con enfoque en la colaboración con fabricantes tecnológicos y la conversión de estrategias en planes de acción ejecutables. El rol requiere coordinación entre equipos multifuncionales y un enfoque orientado a resultados para impulsar crecimiento y cuota de mercado. Se valorará experiencia en ventas y marketing, habilidades analíticas y capacidad para trabajar de forma autónoma. #J-18808-Ljbffr

Job Responsibilities Serves as a statistical department resource, mentors biostatisticians on job skills, oversees or develops training plans or materials for Biostatistics associates. Conducts training sessions, or otherwise trains new hires and enhances the skills of existing personnel. Prepares Statistical Analysis Plans (SAPs), including development of well‑presented mock‑up displays for tables, listings, and figures. Collaborates with sponsor, if required. Responsible for the statistical aspects of the protocol, generation of randomization schedule, and input to the clinical study report. Reviews SAS annotated case report forms (CRFs), SAS database design, and other study documentation to ensure protocol criteria are met and all data is captured as required to support a high‑quality database and the planned analysis. Creates or reviews programming specifications for analysis datasets, tables, listings, and figures. Directs the activities of other biostatistics personnel on assigned projects to ensure timely completion of high‑quality work. Provides independent review of project work produced by other statisticians in the department. Implements company objectives, and creates alternative solutions to address business and operational challenges. Serves as biostatistics representative on project teams, interfacing as necessary with other departmental project team representatives. Includes preparing in advance for internal meetings, contributing ideas, and demonstrating respect for opinions of others. Conducts and participates in verification and quality control of project deliverables, ensuring that output meets the expected results and is consistent with analysis described in SAP and specifications. Manages scheduling and time constraints across multiple projects, sets goals based on priorities from management, discusses time estimates for completion of study‑related activities with biostatistics management, adapts to timeline or priority changes by reorganizing daily workload, and proactively communicates to biostatistics management any difficulties with meeting these timelines. Monitors progress on study activities against agreed‑upon milestones and ensures the study timelines for project deliverables are met. Identifies out‑of‑scope tasks and escalates to management. Provides statistical programming support as needed. May participate in Data Safety Monitoring Board (DSMB) and/or Data Monitoring Committee (DMC) activities, including charter development and serving as an independent non‑voting biostatistician. May serve as a voting statistician on DSMBs and/or DMCs. Leads projects involving integrated analyses, attends regulatory agency meetings or responds to questions, as needed, to support the statistical analysis results of clinical trials on behalf of the sponsor. Provides input, reviews, and subsequently follows applicable Standard Operating Procedures (SOPs), Work Instructions (WIs), and relevant regulatory guidelines (e.g., International Conference on Harmonization (ICH)). Maintains well‑organized, complete, and up‑to‑date project documentation, and verification/quality control documents and programs; ensuring inspection readiness. Displays willingness to work with others and assists with projects and initiatives as necessary to meet the needs of the business. Prepares in advance for internal meetings, contributes ideas, and demonstrates respect for opinions of others. Supports business development activities by contributing to proposals, budgets, and attending sponsor bid defense meetings. Performs other work‑related duties as assigned. Minimal travel may be required. Summary This position is responsible for leading projects across multiple studies or programs. A Principal Biostatistician acts as the primary contact with the sponsor for all biostatistics related activities on assigned projects. Provides external statistical consultancy for sponsor companies, and serves as a departmental resource for complex statistical questions, study design considerations, and protocol development. Core Responsibilities. 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. #J-18808-Ljbffr

Eroski S. Coop. busca incorporar a un profesional para realizar exámenes visuales y evaluaciones de la salud ocular, con atención personalizada y asesoramiento técnico sobre lentes y monturas. El puesto ofrece contrato indefinido, salario bruto anual de 34.553 euros, desarrollo formativo y oportunidades de crecer dentro del equipo; entorno de trabajo colaborativo y enfoque en la salud visual. #J-18808-Ljbffr

Accenture is seeking experienced Software professionals at Team Lead to Manager level to join a cutting-edge AI project. The role is based in Madrid or Barcelona in a hybrid model, with residence in Spain required. You will design and develop microservices using Java/Spring Boot or Python/Fast API, lead cloud-native implementations in AWS, and mentor teams to deliver AI-enabled backend services. Ideal candidates have 6+ years in software development, strong microservices experience, and fluency #J-18808-Ljbffr

Dotgainen en Cataluña busca un Tech Account Executive para liderar la prospección de negocio en servicios de infraestructura, cloud y ciberseguridad. El candidato que se incorpore dirigirá procesos de ventas con un enfoque consultivo y técnico, facilitando que nuevos clientes comprendan cómo Dotgainen puede resolver sus necesidades. Se ofrece contrato indefinido, modalidad 100% remota con visitas a clientes, un salario fijo más comisiones, y un entorno laboral dinámico con oportunidades de desarrollo profesional. #J-18808-Ljbffr

At Roche Diagnostics Solutions (RDS), our mission is clear: to diagnose earlier, develop faster, and personalise treatment because every patient is unique. Our Clinical Development & Medical Affairs (CDMA) team drives innovation to improve healthcare outcomes globally. Position Overview As a Clinical Site Manager for Continuous Glucose Monitoring studies in our Study Delivery Near Patient Care CVMD team, you are responsible for designing, planning, coordinating, and conducting all activities involved in initiating, monitoring, and completing clinical research studies at the clinical study sites. You ensure studies are delivered, recorded, and reported in accordance with protocol, standard operating procedures, good clinical practices, and other applicable regulatory requirements. Responsibilities Act as the primary contact and clinical trial expert for assigned study site personnel, coordinating training, certification, and providing technical assistance to ensure successful study execution. Perform site assessments and qualification visits to support the site selection decision process and site activation activities, including contracting and obtaining IRB/EC/Health Authority approvals in compliance with regulatory requirements. Develop and manage key study site documentation such as Study Monitoring Plans, informed consent documents, source documents, patient instruction guides, and case report forms, while contributing technical expertise to review study protocols, data management plans, reports, and manuscripts. Oversee CROs for the delivery of site management activities, including training CRO CRAs, escalating issues, and collaborating with international investigators and key customers while mentoring and supporting colleagues to enhance their skills and expertise. Execute site management activities for sponsored studies in assigned focus areas across all phases of study (start‑up, conduct, and close‑out) for both registrational and non‑registrational purposes. Validate product performance claims, supply data for critical regulatory submissions, define the functional and clinical utility of products, and gather feedback and opinions from laboratories or customers regarding the products. Work in local and global study teams, including virtual teams, demonstrating diversity, cultural awareness, and fostering strong, collaborative relationships with cross‑functional team members, internal stakeholders, and external partners to achieve business goals and ensure operational excellence. Qualifications Bachelor’s degree in Science, preferably in Health Sciences such as Clinical Diagnostics or Engineering (or equivalent combination of education and work experience). Working experience in the Medical Device or Diagnostics industry, and solid experience in clinical study of IVD/Medical Device/Drug. Experience particularly in the Continuous Glucose Monitoring field. Excellent understanding of ISO14155:2026, MDR, and ICH GCP guidelines in the execution of clinical trials. Ability to make sound decisions, analyze and solve problems, and take responsibility for independent choices. Demonstrates flexibility and adaptability to perform in a fast‑paced, matrixed environment where fluid, cross‑team collaboration is crucial. Where pay transparency applies, details are provided based on the primary posting location. For this role, the primary location is Motherwell. If you are interested in additional locations where the role may be available, we will provide the relevant compensation details later in the hiring process. Roche is an Equal Opportunity Employer. #J-18808-Ljbffr

Alignerr is seeking a Nursing Informatics Specialist (AI Training) to leverage real‑world nursing expertise in evaluating AI‑generated clinical content. This fully remote, hourly contract role offers flexible, asynchronous work and the chance to influence AI understanding of nursing workflows and patient care documentation. You will review EHR-related outputs, provide actionable feedback, and collaborate across teams to improve AI outputs while maintaining clinical accuracy and patient safety #J-18808-Ljbffr