Perfil magisterio para clases de nutrición - ferias-mercados

Descripción del puesto En Spanglish English Academy, buscamos un/a profesor/a de inglés altamente cualificado/a para unirse a nuestro equipo de clases online. Nuestro objetivo es ofrecer formación de calidad que ayude a los alumnos a alcanzar sus metas, especialmente en la preparación de exámenes oficiales de Cambridge. El puesto tendrá el objetivo de preparar exámenes de Cambridge a nivel B2 y C1 de manera intensiva (6 horas semanales por nivel, dando un total de 45 horas por nivel). Requisitos indispensables • Dominio experto de inglés: C2 acreditable (Cambridge C2 Proficiency/CPE o equivalente)., • Nivel bilingüe en español o mínimo C1 (se evaluará en la entrevista)., • Más de 5 años de experiencia enseñando inglés., • Mínimo 3 años de experiencia preparando exámenes de Cambridge (FCE y CAE obligatoriamente)., • Titulación universitaria relacionada con la enseñanza del inglés o la educación., • Residencia en España., • Experiencia y conocimientos en enseñanza online., • Equipamiento disponible para dar clases online., • (Opción de contratar a autónomos). Calendario y disponibilidad • Incorporación: 7 de enero (aunque hay opción de poder incorporarse el 12 de enero)., • Duración del curso: del 7 de enero al 26 de febrero. Opción a extender el contrato hasta junio gracias a los intensivos bimensuales (según disponibilidad y necesidades. NO ES OBLIGATORIO). Habrá otras dos ediciones más de intensivos en marzo-abril y mayo-junio., • Horario: lunes a jueves de 17:00 a 20:00. Habrá opción de trabajar viernes de tarde y sábados de mañana pagando dichas horas como horas complementarias para hacer Speaking (ESTO ES OPCIONAL). Qué ofrecemos • Trabajo 100% remoto (desde casa) dentro de España., • Mejora en el equipamiento si es necesario., • Vacaciones pagadas en Semana Santa y festivos según calendario académico nacional., • Sueldo muy competitivo, claramente por encima del convenio., • 12 horas semanales garantizadas (habiendo opción a horas complementarias siempre y cuando se quiera), • Descanso de 5-7 minutos en mitad de la jornada de 3 horas totalmente remunerado., • Pago adicional por correcciones de redacciones y preparación de clases.

The Senior Clinical Project Manager reports to the Clinical Operations Manager and is responsible to manage the local and international projects in compliance with contractual requirements, timelines, standard operating procedures and relevant regulations and legislations. He/she leads the internal study team allocated on his/her projects ensuring that all deliverables meet agreed expectations and milestones. Establishes with the study team strategies for achieving the study/investigation commitment. Collaborates with major functional areas to identify and evaluate potential issues on the project and ensures the implementation of timely solutions. Proactively manages project level operational aspects including management of trial timeline, budget, and vendors. Forecasts units/hours/generic resources for monitoring activities and analyzes forecasted and worked activities to ensure adherence to contract and budget identifying/escalating any out of scope. Some of what you'll that: • Proactively manages and coordinates the overall project activities ensuring that the deliverable meet contractual requirements, timelines, and quality standard;, • Leads the clinical project team and the various study team meetings;, • Organizes and prepares kick-of meeting, periodic meeting with Sponsor, Investigators’ meeting and internal project meetings ensuring that meeting minutes are appropriately filed in the Trial Master File;, • Provides efficient updates on study/investigation progress to the Sponsor and to the internal team; Prepares feasibility questionnaires and ensures that the site feasibility and qualification process for identification of qualified investigational sites is conducted as per study/investigation requirements and within timelines;, • Prepares the project plans, study/investigation specific procedure and tools;, • Manages study/investigation IMP/IP/MD (i.e., re-supply/IMP/IP/MD expiration/re-labelling of IMP/IP/MD, etc.)  Manages study/investigation materials (questionnaires, sample kit, etc.) Collaborates effectively with the Regulatory and Submission team to speed up the regulatory process and site contract negotiation;, • Reviews and approves the Investigator’s Folder and Trial Master File prototype;, • Ensures that the monitoring team is trained on study/investigation specific procedures and aspects;, • Ensures that the enrolment curve is on-track and take actions in case of under-performance; Ensures that the monitoring activities are conducted as per monitoring plan requirements;, • Reviews and approves site/remote reports;, • Ensures tracking, follow up and resolution of site issues have been completed in a timely manner; Proposes and guarantees the implementation of action plans that resolve issues and/or improve processes;, • Properly and timely escalates relevant issues according to the relevant procedures;, • Ensures potential study/investigation risks are assessed, managed, and communicated according to the relevant procedures., • Manages the administrative aspects of studies/investigations, including study/investigation budget and interact with the Finance and Administrative Unit in case of extra-budgets are needed; Interacts with the Vendor Manager in evaluating vendors services based on study/investigation requirements;, • Manages the study/investigation vendors and monitor the quality of vendor deliverables, addresses quality issues with the appropriate team member and identifies opportunities to improve the execution of the activities;, • Reviews vendor invoices and ensures that hospital fees are paid as per contractual requirements; Ensures all project level study/investigation documentation is filed in the TMF in accordance with company SOPs/all regulatory requirements and provides oversight to the study/investigation team regarding TMF filing, maintenance and archival procedures;, • Ensures that the site TMFs are checked by the monitoring team according to OPIS and/or Sponsor procedures;, • Keeps track of terminating studies and do the final check of the completeness of TMFs;, • Provides support with proposal development and participates in client presentations and/or bid defense meetings, as required;, • Performs co-monitoring visits with CRAs, if necessary;, • Can conduct Feasibility, Pre-study Visit, Site Initiation Visit, Monitoring Visit or Close out visit as necessary (e.g., back-up or directly allocated to the site), if he/she is compliant with local minimum requirements for monitoring;, • Collaborates in establishing and maintaining SOPs related to his/her activities;, • Collaborates to on-boarding of new associates and act as a mentor of junior staff., • Performs and completes on time all required trainings (training on OPIS and/or Sponsor SOPs, all other applicable trainings) by the assigned due date., • Ensures compliance of his/her study team on completing in due time all required assigned study-specific trainings;, • Ensures that OPIS and Sponsors’ KPI/KQI are respected;, • Ensures daily completion of TRACK system, correct entry of appropriate billable and non-billable time and ensure that the activities are billed on time What you have: • Degree in a scientific field, • At least 7 years of experience as Clinical Project Manager, • Excellent knowledge of ICH-GCP, ISO1455 and techniques for the monitoring of clinical trials, • Able to coordinate all the activities related to the management of local and international projects, monitoring of clinical studies/clinical investigations, guaranteeing the security of information, • Able to work independently under the supervision of the Clinical Operations Manager, • Good ability to manage and coordinate resources, • Excellent knowledge of English language, • Able to oversee the activities of CRAs Who we are: Founded in 1998 in Italy and now operating at an international level, OPIS is a full-service science driven biotech focused CRO providing premium trial management for multi-country clinical trials, including state-of-the-art information technology solutions and innovative approaches to the increasing complexity and variety of current projects. OPIS added value lies in its highly specialized professionals who can assist their clients using their deep know-how and experience to guarantee a top-quality level of Clinical Trial Management and ability to operate in a wide range of fields (medical writing, scientific and statistical consultancy for trial design, regulatory activities, pharmacovigilance, etc.) always contributing to our clients’ challenging achievements. What we offer: We offer a competitive salary with other benefits/bonuses and opportunity to develop your professional career with an expanding and growing company. Please read the information notice on the processing of personal data in the candidates information section of our company website.

The Company Our customer is a very innovative company which aims to positively impact on the planet and people’s lives, by providing detailed information and insights about daily changes on the surface of the Earth to empower organizations and businesses to make better decisions. They have a startup mindset with a very solid funding fostering a very quick growing process, and you can grow with them! They will hire the selected candidate as an internal and permanent employee Description of the position We’re looking for a Network Engineer for its global operations in Madrid. He/She will be play a critical role in managing and optimizing company’s network infrastructure. Working Experience @ 3–5 years of hands-on experience in network engineering or a similar role. This includes experience in designing and managing enterprise networks (LAN/WAN), configuring network equipment. Tech skills @ Excellent at diagnosing and resolving complex network issues quickly and under pressure. @ Strong understanding of networking protocols and systems. Proficient with TCP/IP, routing (e.g., OSPF, BGP) and switching (VLANs, STP), and experienced with enterprise network hardware (routers, switches, firewalls, APs). @ Hands-on experience with network security devices and concepts. @ Knowledge of ITIL or similar IT service management frameworks. Soft skills @ Experience working in a multi-national environment or on international teams. @ Excellent communication and interpersonal skills. @ Excellent problem-solving and analytical skills. @ Team-oriented attitude. Key Responsibilities @ Manage Network Architecture & Topology Design: Plan and develop the network’s structure (LAN, WAN, Wi-Fi) to meet business needs, ensuring the design is scalable, secure, and well-documented. @ Network Hardware Management: Install, configure, and maintain network devices (switches, routers, firewalls, access points) in the office and data center, keeping all equipment updated and running optimally. @ Performance Monitoring & QoS: Use network monitoring tools to track performance and reliability. Implement Quality of Service policies to prioritize critical traffic, so important data (e.g., voice or video) isn’t delayed or dropped during congestion. @ VLAN Configuration & Segmentation: Set up and manage Virtual LANs to segment network traffic for security and efficiency. @ Connectivity Redundancy: Implement redundant links and failover paths to achieve high availability ensuring the network stays up even if a primary connection or device fails. @ ITIL-Compliant Operations: Follow ITIL processes for network changes and incidents. @ Cross-Team Collaboration: Work closely with other IT teams (cloud, security, workplace) and vendors/partners. Provide network support in projects (such as new software rollouts or office expansions) and ensure external providers meet agreed service levels. @ Documentation & Policy: Maintain up-to-date network documentation, including diagrams, device configurations, IP address inventories, and failover procedures. Develop standard operating procedures for routine tasks and troubleshooting, to facilitate knowledge sharing and consistency. @ Continuous Improvement: Regularly evaluate the network setup for improvements. Stay informed about new networking technologies (SD-WAN, Wi-Fi 6/7, automation tools) and propose upgrades or optimizations that enhance performance, security, or efficiency. @ Management Advisement: Provide recommendations to IT leadership on network capacity planning, infrastructure investments, and design improvements. @ Security & Compliance: Work with the information security team to safeguard the network (ensure firewall rules, VPN access, and intrusion prevention systems are effective). Ensure all network activities comply with company policies and relevant regulations (e.g., data protection laws). Languages @ Spanish: At least B2 @ English: At least C1. Job location Tres Cantos (Madrid). European Union citizen; otherwise, a valid job permit is mandatory. Salary A very competitive salary package. Working from home 3-4 days a week (but according to the specific needs that may arise from the perspective of project development, department, clients, and/or partners). If you are interested, please apply here or send us an email to including in the subject: ‘Network Engineer’ along with your CV in English.

RESUMEN DEL CANDIDATO/A BUSCADO/A En Premium Research buscamos un/a Investigador/a en Inteligencia Artificial y Machine Learning (PhD) para reforzar nuestro equipo de I+D. La persona seleccionada participará en el diseño, desarrollo y despliegue de modelos avanzados de IA en proyectos de investigación aplicada, principalmente, en el ámbito de la salud (aunque no exclusivamente), trabajando en entornos altamente técnicos, colaborativos y multidisciplinares. DESCRIPCIÓN DEL PUESTO La persona incorporada formará parte del área de Inteligencia Artificial y Machine Learning de Premium Research, contribuyendo activamente a proyectos estratégicos de I+D a nivel nacional y europeo. Su labor abarcará desde el diseño conceptual de modelos y metodologías avanzadas hasta su implementación técnica y validación, colaborando estrechamente con perfiles investigadores, ingenieros y expertos en el ámbito biomédico. Entre sus principales responsabilidades se incluyen: • Diseño, desarrollo y validación de modelos de Machine Learning y Deep Learning aplicados a problemas complejos., • Análisis y procesamiento de grandes volúmenes de datos, incluyendo datos biomédicos y de salud, entre otros., • Desarrollo de pipelines de datos y modelos, desde la fase de investigación hasta su despliegue., • Colaboración en proyectos de I+D+i, incluyendo consorcios europeos y nacionales., • Elaboración de documentación técnica, informes científicos y apoyo a publicaciones científicas cuando proceda., • Trabajo en entornos cloud, DevOps y MLOps para el escalado y mantenimiento de soluciones de IA. Se valorará especialmente la experiencia o especialización en el ámbito de la salud, incluyendo proyectos de bioinformática, biomedicina o salud digital, así como experiencia en dry lab (análisis computacional de datos biomédicos) y, de forma adicional, conocimientos de wet lab, técnicas de laboratorio y procesamiento de muestras, que permitan una comprensión integral del ciclo experimental y su traducción a datos y modelos de IA. El puesto ofrece la oportunidad de integrarse en un entorno investigador de alto nivel, con participación en proyectos punteros financiados en gran parte por la Unión Europea, y con una clara orientación a la excelencia científica y tecnológica. REQUISITOS: Experiencia profesional • Mínimo 3–5 años de experiencia en investigación aplicada, I+D o desarrollo avanzado en Inteligencia Artificial y Machine Learning, en entornos académicos, industriales o mixtos., • Experiencia demostrable en:, • Diseño, desarrollo, entrenamiento y validación de modelos de Machine Learning y Deep Learning., • Análisis y procesamiento de grandes volúmenes de datos y pipelines complejos., • Participación en proyectos de I+D+i, preferentemente a nivel nacional y/o europeo., • Experiencia en el desarrollo de soluciones de IA desde fases de investigación hasta su implementación técnica., • Valorable experiencia previa en proyectos del ámbito de la salud, biomedicina, bioinformática o salud digital, incluyendo trabajo con datos biomédicos. REQUISITOS: Formación Doctorado (PhD) en una de las siguientes áreas o disciplinas afines: • Inteligencia Artificial, • Machine Learning / Data Science, • Bioinformática / Computación, • Matemáticas, Física, • Ingeniería de software Sólida formación en matemáticas y estadística, aplicada al modelado y análisis de datos. CONOCIMIENTO, HABILIDADES Y COMPETENCIAS CLAVE Imprescindibles: • Elevado nivel de matemáticas., • Experiencia avanzada en Machine Learning e Inteligencia Artificial, • Dominio avanzado de Python., • Programación de software., • Nivel avanzado de inglés hablado y escrito., • Modelos supervisados y no supervisados., • Deep Learning y arquitecturas avanzadas., • Capacidad de trabajo autónomo y en equipos multidisciplinares., • Responsabilidad, eficiencia y capacidad de esfuerzo. Deseables: • Conocimientos de ingeniería de software., • Cloud engineering., • DevOps., • Experiencia en entornos cloud (AWS, GCP, Azure u otros)., • Escalado y mantenimiento de soluciones de IA en producción., • Habilidades transversales: comunicación, síntesis, capacidad analítica, etc., • Experiencia en proyectos de salud. CONDICIONES DE TRABAJO Y SALARIO: • Contrato indefinido, con 6 meses iniciales de prueba., • Jornada completa., • 100% teletrabajo desde cualquier punto de España., • Flexibilidad para elegir horario y vacaciones., • Jornada intensiva sólo por las mañanas los meses de julio y agosto., • Disponibilidad para reuniones presenciales cada 1-2 meses y posibles viajes al extranjero 1-2 veces al año., • Puesta a disposición de teléfono de empresa y equipos informáticos de última generación., • Rango salarial orientativo: 32.000 € - 38.000 € euros brutos anuales, en función de la experiencia, formación y capacidades. El puesto incluye un plan de crecimiento y revisión salarial según la progresión del candidato/a. NUESTRA EMPRESA Premium Research es una empresa de base tecnológica especializada en la prestación de servicios de ciencia e innovación y en el desarrollo de proyectos de I+D+i tanto a nivel europeo como nacional. Cuenta con un equipo multidisciplinar con experiencia en biomedicina, nanotecnología, genética, bioinformática y machine learning, y ha participado en proyectos de alto impacto en ámbitos como la salud, la economía circular y smart cities entre otros. En su área de Data Science, Premium Research destaca en la gestión de grandes volúmenes de datos, la bioestadística y el modelado predictivo, además de liderar iniciativas propias de desarrollo de producto e innovación.

🧬 Are you passionate about clinical research and eager to be part of projects that directly impact people’s health? You will join a strategic project within a leading pharmaceutical company, working closely with medical teams and investigators, and actively participating in all phases of clinical studies, from study start-up to close-out. 🎯 What do we offer? Permanent contract through Manpower to provide services on a project within a top-tier pharmaceutical company. A high-impact project focused on clinical research and the development of innovative medicines. A collaborative environment with continuous training and close interaction with multidisciplinary teams. 🔬 What will your day-to-day look like? You will be responsible for monitoring and following up on clinical studies at assigned investigator sites, ensuring compliance with the protocol, Good Clinical Practices (GCP), and regulatory requirements. Your main responsibilities will include: Conducting study initiation, monitoring (on-site and remote), and close-out visits. Verifying the quality and accuracy of clinical data and the correct management of informed consent. Overseeing adverse event reporting and ensuring ethical and regulatory compliance. Keeping study documentation up to date and preparing visit reports. Providing ongoing support to investigators to ensure proper patient recruitment and follow-up. 🌟 What are we looking for? University degree in health sciences, biology, pharmacy, medicine, or related fields. Previous experience as a Clinical Research Associate or in clinical research (experience in observational or clinical studies is highly valued). Good knowledge of Good Clinical Practices (GCP) and applicable regulations. Strong analytical skills, attention to detail, and a focus on data quality. Good communication skills, autonomy, and the ability to manage multiple sites and tasks. High level of confidentiality, professional ethics, and scientific rigor. 🚀 Apply now and take the next step in your career in clinical research!

Due to our ongoing global expansion, we have a great opportunity for a Regulatory Submissions Specialist to join our growing regulatory team in Taiwan, on a fully remote basis. We are looking for someone who can autonomously carry on the work within the scope of their activities and interacts with the Direct Manager to define priorities and manages workload. The Regulatory Submissions Specialist contributes to the management and development of procedures related to the activities in which he/she is involved in and ensures that the outputs of their activities meet the quality standards required by the company. Ensures the timely compilation of activity tracking and attendance systems. What you'll do: • Develops and maintains knowledge of global and local regulatory requirements and industry practice/guidelines for submission activities., • Manages adaptation of master documentation for submission (Informed Consent and any additional patient items such as patient emergency card, patient diary and questionnaires etc…) to local requirements., • Manages activities associated with obtaining initial and amended central authority approvals from Competent Authorities (CAs), Central Ethics Committee (CECs), IRB and any other authorities, • Manages contract and budget negotiation/execution with sites/investigators/other parties involved as applicable., • Prepares the financial agreement/addendum to the financial agreement/loan/assignment letter for an external structure and obtain the Sponsor/OPIS signatures for the shipment to the Site., • Maintains tracking of regulatory, ethics and administrative submission and approval dates. What we are looking for: • Experience with CA and CEC submission, using combined ways of submission, • ICF customization;, • Contracts and budget negotiation,, • CTIS (The Clinical Trials Information System) experience - a new central way how EU submission are being processed, • Minimum 2 years’ experience in a pharmaceutical or Clinical Research Organization, • Good knowledge of ICH / GCP regulations / IRB, • Fluent in English, • Good planning, problem solving and organizational skills What we offer: We offer a competitive salary, bonuses, and other benefits together with the opportunity to develop your professional career with an expanding and growing international company. Please read the information notice on the processing of personal data in the candidates’ information section of our company website. Who we are: OPIS is an International CRO with 25 years of experience in conducting Phase I-IV, non-interventional and medical devices studies on an international level. We always offer state-of-the-art information technology solutions and innovative approaches to the increasing complexity and variety of projects. OPIS extensive expertise covers all phases of drug-related trials, taking care of the Sponsor beyond the therapeutic area, offering also accurate clinical investigations for medical and diagnostic devices. With Global Clinical Research Locations all over the world, OPIS offers a full range of integrated clinical research services as scientific advice, medical writing, trial start-up, monitoring, study management, data management, statistics, pharmacovigilance, medical monitoring, electronic data capture as well as quality assurance and training.