MONITOR/A DE AJEDREZ - Docendo Ocio Educativo - Vitoria-Gasteiz

At Faes Farma, where we unite passion, science and innovation to transform people's health, we are looking to incorporate a Research Scientist in Medicinal Chemistry. We are seeking to add to our Drug Discovery R&D team a professional with a strong background in medicinal chemistry who will contribute to the design and development of new chemical entities with therapeutic potential. What will your mission be? Actively participate in drug discovery projects, from defining scientific strategies to compound optimization, contributing to the advancement of drug candidates. Main responsibilities • Contribute to the definition of project objectives and scientific strategies., • Design and synthesize new chemical entities applying knowledge of organic and medicinal chemistry., • Progressively lead workstreams within medicinal chemistry projects., • Manage compound optimization based on biological results, ADMETox and profiling studies., • Collaborate with multidisciplinary teams (biology, ADMET, pharmacology, etc.)., • Use computational tools and collaborate with external partners to accelerate projects., • Maintain high laboratory productivity standards through efficient planning., • Analyze results, prepare reports and communicate progress to the team., • Participate in the drafting of patents, scientific publications and technical documentation. Requirements • Bachelor’s or Master’s degree in Chemistry or Pharmacy., • PhD in Organic Chemistry, Medicinal Chemistry or related field., • Minimum of 2 years of experience in a pharmaceutical environment or academic laboratory in organic/medicinal chemistry., • Strong experience in organic synthesis (multi-step synthesis), purification and characterization., • Knowledge of ADMETox properties and PK/PD relationships., • High level of English (spoken and written). Preferred qualifications • Experience in flow chemistry, parallel synthesis or automated platforms., • Interest or experience in the use of artificial intelligence and machine learning applied to drug discovery., • Ability to identify and solve problems independently., • Strong communication and teamwork skills in multidisciplinary environments., • Experience or knowledge in ophthalmology (a plus).

Descripción de la empresa INTERNATIONAL SCHOOL ANITA CONRAD SL es una empresa situada en Las Palmas, España, dedicada a ofrecer educación de calidad. Su visión se centra en crear un entorno de aprendizaje integral y multicultural para los más pequeños, fomentando el desarrollo académico y emocional. La empresa opera desde sus instalaciones en la Calle Lomo Los Azules y es conocida por su enfoque innovador hacia la enseñanza. Descripción del puesto Como Educador/a Infantil y/o Maestro de Infantil/Primaria serás responsable de organizar y llevar a cabo actividades educativas diseñadas para fomentar el desarrollo temprano de los niños. Entre tus tareas diarias, te encargarás de crear un ambiente estimulante, guiar a los niños en sus aprendizajes, y mantener una comunicación dinámica con las familias. Este es un puesto de tiempo completo, que se realizará de manera presencial en San Bartolomé de Tirajana. Requisitos • Aptitudes interpersonales y capacidad para colaborar eficazmente con otros educadores y familias., • Conocimientos en desarrollo infantil temprano y experiencia previa trabajando con niños pequeños., • Habilidades de creatividad para diseñar actividades atractivas que favorezcan el aprendizaje y el desarrollo personal de los niños., • Organización y planificación para gestionar tareas administrativas y preparar actividades educativas con antelación., • Competencia en idiomas inglés avanzado y formación certificada en educación infantil serán v requisitos necesarios,

About the Company Virtus College, The British Sixth Form, is the first Sixth Form College in Spain, offering a British education in small class sizes and year groups. Founded in 2016, we have built a distinctive educational model centred on academic excellence, personal development and a highly personalised approach to teaching and mentoring. Over the past nine years, Virtus has grown significantly and now operates from a state-of-the-art campus in La Moraleja, Madrid. Our model combines the academic rigour of the British Sixth Form system with a strong commitment to student wellbeing, university guidance, and the development of the skills students need to thrive in the 21st century. At Virtus, every student follows a personalised Roadmap designed around their academic profile, aspirations and university goals. Our teachers play a central role in making that journey successful, not only through high-quality classroom teaching, but also through mentoring, enrichment and active participation in the wider life of the school. We are a close-knit, international team united by a shared commitment to educational excellence, innovation and the belief that every student can become the best version of themselves. About the Role We are seeking a passionate and committed Physics A-Level Teacher to join our teaching team from August 2026. The successful candidate will teach Physics at KS5 / A-Level, contributing to a learning environment that is intellectually ambitious, highly supportive and rooted in strong relationships with students. This is a dynamic role that extends beyond subject teaching and includes involvement in our Mentoring Programme, The Enrichment Programme, and the broader pastoral and co-curricular life of the school. Responsibilities Teaching and learning • Teach Physics at A-Level standard, ensuring excellent subject knowledge, strong exam preparation and high academic expectations., • Plan and deliver structured, engaging and challenging lessons in line with Virtus’ teaching approach and the principles of ACE: Assessment, Challenge and Engagement., • Adapt teaching to support, stretch and challenge students of different abilities and profiles., • Integrate digital tools and ICT effectively into teaching and learning, in line with Virtus’ technology-rich educational model., • Design, implement and review both formative and summative assessments in line with curriculum goals and examination requirements., • Provide students with regular, meaningful and actionable feedback to support progress. Student progress and pastoral contribution • Monitor student performance carefully and maintain accurate records of attendance, grades and progress., • Report on student progress clearly and professionally, including in communication with families and at parents’ evenings., • Contribute to the pastoral life of the school and support the wellbeing and development of all students., • Take responsibility for mentees within the Mentoring Programme, working closely with the Head of Mentoring and the wider team to support students in their academic, personal and university-related goals. Wider school contribution • Contribute actively to The Enrichment Programme, including the design and/or delivery of co-curricular opportunities, clubs or societies, depending on the candidate’s profile and interests., • Attend staff meetings, CPD sessions, parents’ evenings, school events, outings and other relevant school activities., • Uphold and promote the ethos, values and professional standards of Virtus at all times., • Remain up to date with safeguarding, school policies, educational standards and best practice. Qualifications • Degree-level qualification directly related to Physics, or a closely related field., • Ability to teach Physics at KS5 / A-Level., • Previous classroom teaching experience., • High level of English, both spoken and written., • Strong communication, organisational and interpersonal skills., • Ability to deliver engaging, inclusive and academically ambitious lessons., • Commitment to safeguarding and to the holistic development of young people., • A collaborative mindset and willingness to contribute to the wider life of the school. Required Skills • PGCE, UK QTS, or equivalent postgraduate teaching qualification., • Experience teaching A-Level or within the British curriculum., • Experience using digital devices and educational technology in the classroom., • Experience in mentoring, pastoral care or university guidance., • Experience contributing to enrichment, co-curricular activities, clubs or societies., • Evidence of continued professional development in subject knowledge or pedagogy. Pay range and compensation package • Permanent contract under the Spanish system., • Salary: €34,000-€38,000 gross annual salary, depending on experience and aligned with market conditions. Additional salary progression of €1,500 gross per year, subject to performance, during the first three years after signing., • Start date: August 2026. Schedule: on site, 08:15 to 16:30, Monday to Friday, with occasional later finishes for events and meetings., • Extensive support, induction and training. Access to high-quality teaching resources and a technology-rich environment., • Free cooked lunches and hot drinks every day., • Public transport costs covered., • Free access to sports facilities through Wellhub (Silver Plan)., • Full support with legal and administrative visa processes where applicable. Equality, Diversity and Inclusion Virtus College is committed to promoting equality, diversity and inclusion across the whole school community. We warmly welcome applications from candidates of all backgrounds and are committed to creating an environment in which all staff and students feel respected, safe and valued.

At Faes Farma, where we unite passion, science and innovation to transform people’s health, we are looking to incorporate a Clinical Research Head to join our team. As the Clinical Research Physician Head you will be responsible for the scientific leadership of clinical research activities within the Clinical Research Department. You will operate in a wide range of aspects in clinical and pharmaceutical medicine, providing scientific and therapeutic expertise in the Company interactions with health authorities, health care providers, colleagues, and contract research organisations (CROs). Your role will be focused on overseeing medical activities in phase I–IV clinical trials, ensuring compliance with ethical, legal, and regulatory standards; as well as participating in the elaboration of clinical development plans and scientific divulgation. You will line-manage and develop the scientific group of the department and will report to the Global Head of the Department. Key responsibilities: • Lead medical oversight of clinical trials (Phase I–IV), • Contribute to clinical development plans and pipeline strategy, • Support go/no-go decisions based on scientific and operational insights, • Ensure compliance with regulatory requirements and ICH-GCP standards, • Lead, develop and inspire a team of Clinical Scientists and Medical Experts, • Collaborate cross-functionally with Regulatory Affairs, Medical Affairs, and other key stakeholders, • Support interactions with health authorities and regulatory agencies What we are looking for: • Medical Degree (Ophthalmology preferred), • +5 years of experience in clinical research or clinical development, • Strong knowledge of ICH-GCP and regulatory frameworks, • Proven leadership and team management experience, • Excellent communication skills in English and Spanish

En UTAMED buscamos un/a docente de inglés universitario con acreditación de ANECA. ❗ Requisitos imprescindibles • Acreditación de Contratado Doctor o Profesor de Universidad Privada por ANECA, • Experiencia docente universitaria., • Nivel alto de inglés (C1–C2 o docencia en inglés demostrable). 🎯 Funciones • Impartición de asignaturas de inglés en distintos grados., • Evaluación del alumnado con criterios académicos., • Desarrollo y actualización de contenidos., • Acompañamiento al estudiante en su aprendizaje. 💡 Se valorará • Experiencia en entornos de educación online., • Participación en proyectos de innovación docente., • Experiencia profesional internacional o en empresa. 🌍 Sobre UTAMED UTAMED es una universidad online comprometida con la innovación educativa, la calidad académica y el impulso de la actividad investigadora. En el marco de su crecimiento institucional, UTAMED abre una convocatoria para la incorporación de Personal Docente e Investigador (PDI) con el objetivo de reforzar su claustro académico y potenciar el desarrollo de líneas de investigación vinculadas a sus titulaciones. 💡 Lo que ofrece UTAMED • Contrato laboral indefinido, • Docencia 100 % online con flexibilidad real, • Ecosistema digital con aulas virtuales interactivas, • Entorno académico orientado al desarrollo de la carrera investigadora, • Posibilidad de participar en proyectos de investigación y producción científica, • Integración en una universidad en crecimiento y expansión 🚀 ¿Te interesa? Si cuentas con acreditación universitaria y experiencia docente, inscríbete en la oferta y forma parte del proyecto UTAMED.

KPS is looking for Oversight Monitor to join sponsor team. Small FTE approx 0.2 for this year. The primary responsibility of the (Clinical) Oversight Monitor (C)OM) is to ensure adequate Sponsor oversight of the conduct, monitoring and management of one or more clinical studies and assigned monitors at clinical study sites, within the assigned country or region. The (C)OM): • contributes to development of the Overall Study Management Plan, the study level Site and Monitoring Plan and the Oversight Monitoring Plan., • contributes to the definition of appropriate standards and quality indicators for site management and monitoring., • ensures high quality conduct and execution of clinical studies at sites according to the protocol and study team and governance requirements in compliance with quality, regional and regulatory (GCP) standards., • addresses issues identified with study conduct, monitoring and site management with Sponsor’s management, are appropriately communicated/escalated and follows up through resolution., • May conduct oversight monitoring visits, co-monitoring visits, monitoring visit report reviews and other Sponsor oversight activities per applicable study plans, as needed., • reviews the submission documents for IRBs/IECs and Health Authorities as appropriate for assigned sites/countries/region., • may assist with translations or verification of translations., • implements approved communication plans with external strategic partners or CROs., • supports the collection of key study performance information, including study start-up metrics, enrollment, data collection timeliness/quality., • reviews monitoring visit reports for finalization/consistency/issues according to study monitoring plan., • utilizes available tools/systems to assess vendor and site performance., • ensures inspection readiness at the study sites and follow up corrective/preventive actions., • maintains good communication and working relationships with investigators, internal stake-holders and external services providers (CROs)., • computer literacy in appropriate software(s)., • the ability to work well within a matrix environment with excellent interpersonal (written and verbal) and decision-making skills., • demonstrated innovation skills, drive, energy and enthusiasm to deliver the study program objectives., • demonstrated management of all clinical study aspects (developing a protocol to clinical study report)., • the ability to identify, solve and escalate issues that arise at study sites and within site management, • comprehensive/extensive knowledge of ICH guidelines/GCP and remains current on medical/scientific aspects., • demonstrated project management skills i.e. (simultaneous management of multiple vendors, sites and studies. Possesses excellent planning, time management and coordination skills., • a degree (BSc/MSc or equivalent preferred) in life science, nursing, pharmacy, medical laboratory technology, or other health/medical related area., • other degrees and certifications considered if commensurate with related clinical research experience (e.g., diploma or associate degree RN, certified medical technologist)., • a minimum of 8+ years’ relevant clinical research (or related) experience., • 6+ years’ experience in monitoring and site management of industry sponsored clinical research (CRA, Clinical Trial Monitor, or equivalent)., • a thorough understanding of the drug development and clinical trial process., • the ability to assess selected CROs monitoring performance and provide constructive feedback and remediation as necessary., • the ability to participate in preparation, conduct and follow up of audits and site inspections., • active management experience of countries and sites in a region., • thorough knowledge of ICH guidelines/GCP and its applicability to all stages of the clinical development process.

🎓 ¿Quiénes somos? UTAMED es una universidad a distancia con un espíritu innovador, inquieto y curioso. Nos adaptamos a los cambios en la educación y en la sociedad, comprendiendo que la búsqueda del conocimiento es un proceso dinámico y en constante evolución. Nuestra misión es ofrecer programas académicos alineados con las exigencias del mundo actual, potenciando el desarrollo personal y profesional de nuestros estudiantes. 🔎 ¿A quién buscamos? Seleccionamos profesionales para colaborar como redactores/as de contenidos y posteriormente como docentes del Grado de Derecho, en la siguiente asignatura: • Derecho de familia y sucesiones. 🎯 Requisitos clave • Doctorado en Derecho., • Acreditación ANECA como Profesor Titular de Universidad (preferiblemente) o Profesor Contratado Doctor., • Especialización en Derecho de Familias., • Interés por la docencia universitaria y la elaboración de contenidos., • Manejo fluido de herramientas digitales y plataformas online., • Disponibilidad para colaborar en modalidad 100% remoto. 🌍 ¿Qué harás en UTAMED? • Redactar y preparar los contenidos y materiales docentes de las asignaturas., • Una vez que comience la asignatura, impartir docencia en modalidad online, • Diseñar actividades y recursos orientados a la práctica profesional., • Acompañar y orientar al alumnado en su aprendizaje., • Participar en la mejora continua del programa formativo. 💡 Valoramos especialmente • Experiencia previa en docencia universitaria o formación., • Participación en proyectos académicos o de innovación educativa., • Buenas habilidades de comunicación y vocación docente. 📄 Condiciones Fase 1 – Redacción y preparación del material formativo (contrato mercantil): • Duración: desde el inicio de la colaboración hasta el inicio del curso., • Docencia asociada a un volumen aproximado de 90 alumnos., • Modalidad 100% online., • Implica impartir clases, supervisar actividades y acompañar al alumnado durante el curso., • 2.800€ por 90 alumnos. 📄 Lo que ofrecemos • Docencia 100% online con flexibilidad real., • Ecosistema digital con aulas virtuales interactivas y analítica de aprendizaje., • Formación continua y Certificación UTAMED en Docencia Online., • Comunidad docente internacional y colaborativa., • Programas Boost y Consolida con mentoría, apoyos y ayudas económicas., • Incentivos por publicaciones y proyectos de investigación., • Apoyo para congresos, estancias y colaboración en grupos emergentes. 🚀 ¿Te interesa formar parte del proyecto? Si eres Procurador/a, te apasiona compartir tu experiencia y quieres participar en la formación de futuros profesionales, ¡te estamos esperando! 👉 Envía tu candidatura y súmate a UTAMED

This is not an on-site or in-house monitoring position. This role is equivalent to an SSU Specialist II. Kapadi is a full service CRO that focuses on complex oncology indications including immunotherapy and cellular therapies. We know that innovative research requires innovative operations and we've built that into our culture, systems and processes. We have an infrastructure to enhance access to patients and integrated technology to provide higher quality and faster access to results. We are looking for a highly-motivated Research Associate II - Study Start-Up and Maintenance to help us continue to grow our business and deliver new, life-changing therapies for the cancer patients who need them. As a Research Associate II - Study Start-Up and Maintenance, you will: • Perform study startup and regulatory document maintenance activities for Phase I-IV clinical research projects., • Assess the progress of clinical projects at assigned sites and ensure clinical projects are conducted, recorded and reported in accordance with the protocol, Company and Sponsor standard operating procedures (SOPs), ICH-GCP, and/or all applicable local and federal regulatory requirements., • Serve as the primary liaison between site and project team throughout the study lifecycle, from site identification through close-out related to site start-up support and regulatory document maintenance. Respond to site concerns and questions as applicable., • Document activities via communication logs and other required project documents as per SOPs and project plans. Enter data into tracking systems as required to track all observations, ongoing status and assigned action items for resolution., • Manage, coordinate and perform Central IRB submissions for North America and local CTIS submissions for Europe, including but not limited to: initial submissions, amendment submission, changes of PIs, safety submission, annual reviews etc.., • Assist the project team with the creation and finalization of the Clinical Site Activation Plan. Knowledge, skills and abilities: • Demonstrated knowledge of the clinical research and development process in pharmaceutical and/or biotechnology industries., • Demonstrated ability to lead and coordinate study start-up and regulatory activities for large-scale clinical trials., • Strong knowledge of Good Clinical Practice/ICH guidelines and other applicable regulatory requirements. Requirements: • Bachelor’s Degree (or equivalent) level of qualification in Life Sciences, Medicine, Pharmacy, Nursing or equivalent combination of education and experience., • Minimum of 3 years of experience in clinical R&D in pharmaceutical, biotechnology and/or clinical research organization (CRO) businesses, including at least 2 years of experience in a CRO providing clinical research services to pharmaceutical, biotechnology or medical device companies., • 5+ years of experience in a study start-up position. Candidates who also bring in experience in compiling EU CTR submissions via CTIS in Ireland or even other EU CTR countries and with additional language skills are preferred. This position is homebased!