Buscamos monitor o monitora de ludoteca en Palma - Froggies - Palma

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• Tusclasesparticulares

  

  Monitor/a de Tiempo Libre y Refuerzo Escolar

  3 days ago

  €15–€30 hourly

  Part-time

  Palma

  En Tusclasesparticulares, empresa líder en educación, buscamos monitores/as de tiempo libre con vocación educativa que deseen acompañar a niños y niñas en sus deberes escolares, así como dinamizar actividades lúdicas que fomenten su desarrollo personal y académico. Tareas: • Apoyar a los niños en la realización de sus tareas escolares (primaria, ESO, etc.)., • Organizar y dinamizar actividades de tiempo libre y juegos educativos., • Fomentar una actitud positiva y motivadora hacia el aprendizaje. Requisitos: • No es necesario tener experiencia previa., • Compromiso y responsabilidad en el proceso educativo., • Valorable formación o interés en el ámbito de la animación sociocultural, monitor/a de tiempo libre o refuerzo escolar. Beneficios: • Flexibilidad horaria, • Modalidad hibrida, online o presencial., • Salario: 15€ a 30€/hora ¿Quieres formar parte de un proyecto educativo que combina el aprendizaje con el ocio creativo? ¡Aplica ahora!

  Immediate start!

  No experience

  Easy apply
• Minimon

  

  Monitor/a Infantil

  1 month ago

  €950 monthly

  Part-time

  Palma

  Chiquipark requiere monitor/a para puesto de trabajo. Contrato de larga duración. Incorporación inmediata. Se valorará experiencia previa en puesto similar. Imprescindible nivel medio de inglés y catalán.

  Immediate start!

  Easy apply
• GREEN VALLEY SCHOOL MALLORCA SL

  

  Secondary School Maths Teacher

  2 days ago

  Palma

  Company Description GREEN VALLEY SCHOOL MALLORCA SL is based out of CAMÍ DE LA VILETA, 210, PALMA, Illes Balears, Spain. The school is situated in the Greater Palma de Mallorca Metropolitan Area. Role Description We are looking for an enthusiastic and dedicated Secondary School Maths teacher (KS4 - KS5) to join our exciting Secondary school on the Island of Majorca. We have a talented, welcoming staff and an ethos which is built around teaching human values to our students; developing the whole child alongside high academic expectations. The successful candidate will teach Secondary Maths, covering both IGCSE and IB Diploma programs. Currently we have a successful Nursery and Primary school and after opening our Secondary School in September 2018, we now offer the IGCSE and IB DP curriculums, thus there is huge potential for professional development for our staff. This is a very exciting time to be part of Green Valley. Qualifications • UK qualified in Secondary education or equivalent., • Relevant experience with both GCSE and IB DP curriculums., • Proactive attitude and flexibility, • A love of learning and passion for education, • Enthusiasm for excellence in all areas of school life, • Ideally the candidate will already be living in Spain., • Green Valley School is committed to giving the best education to all our children, widening their horizons and raising their aspirations to prepare them for the modern world., • The successful candidate must be living in Sapin or have the right to work in Spain already. The school can offer • Competitive salary with a pay scale which rewards experience and qualifications., • A happy working environment., • Professional development, • Small class sizes of many nationalities, • A well-equipped classroom in a modern school (finished in 2017), • An encouraging and supportive management team, • Many opportunities for professional development and career advancement, • To start as soon as possible., • Salary: 30,000€ - 34,000€ gross per year., • Permanent contract offered. Please send your CV and a covering letter to: (please only apply if you have the right to work in Spain) humanresources@edu.greenvalleyschool.es https://greenvalleyschool.es/ Timing: 1st September 2026.

• emocional.com

  

  Técnico/a o Maestro/a de Educación Infantil ( IBIZA)

  4 days ago

  Palma

  Ibiza · Presencial · Jornada completa Sobre Emocional En emocional.com somos un centro de psicología y formación que combina lo mejor de la tecnología con lo mejor de las personas. Ayudamos a más de 200 empresas y a más de 20.000 personas cada día a mejorar su salud mental y emocional. En este proyecto ampliamos nuestro impacto al ámbito de la primera infancia, incorporando un equipo educativo especializado para la atención a niños y niñas de 0 a 3 años. Valoramos positivamente la discapacidad acreditada igual o superior al 33%. Sobre el trabajo Buscamos Técnicos/as de Educación Infantil y Maestros/as de Educación Infantil para formar parte de un equipo educativo en Ibiza. El proyecto está dirigido a niños y niñas de 0 a 3 años y se desarrollará desde una mirada educativa, inclusiva, segura y centrada en el cuidado cotidiano. Formarás parte de un equipo estable y cualificado, orientado a garantizar una atención educativa de calidad, en coordinación con las familias, el equipo del centro y los recursos del entorno. Tu día a día Recibirás a niños y niñas durante la acogida, observando su estado emocional, físico y comunicativo. Acompañarás separaciones familiares, llanto, cansancio, sueño, hambre o necesidades de contacto. Organizarás propuestas de juego, exploración, movimiento, cuentos, música, materiales sensoriales, patio y vida cotidiana. Atenderás momentos de higiene, cambio de pañal, lavado de manos, comedor y descanso desde una mirada educativa y respetuosa. Comunicarás a las familias información relevante del día. Registrarás observaciones sobre adaptación, desarrollo, alimentación, descanso, comunicación, juego y relación. Te coordinarás con tutoras, apoyos, dirección y otros recursos cuando sea necesario. Prepararás materiales, espacios y rutinas adaptadas a cada grupo de edad. Participarás en reuniones de equipo, claustros, coordinación de comedor, atención a la diversidad, familias y formación. Aplicarás protocolos de seguridad, protección infantil, igualdad, coeducación, salud y prevención de riesgos. Perfiles que buscamos Buscamos incorporar los siguientes perfiles profesionales: Técnicos/as de Educación Infantil 8 profesionales con titulación de Técnico/a de Educación Infantil o equivalente según la normativa vigente, a jornada completa. Maestros/as de Educación Infantil 2 profesionales con titulación de Maestro/a de Educación Infantil o equivalente según la normativa vigente, a jornada completa. Requisitos y aspectos valorables Titulación Técnico/a de Educación Infantil, Maestro/a de Educación Infantil o titulación equivalente según normativa vigente. Experiencia Se valorará experiencia en escuelas infantiles de primer ciclo y en atención educativa a niños y niñas de 0 a 3 años . Capacidad técnica Capacidad para trabajar en un entorno educativo estable, seguro, inclusivo y adaptado a las necesidades de la primera infancia. Lengua vehicular El catalán será la lengua vehicular y de cohesión, respetando el castellano y las lenguas familiares. Formación anual El personal educativo realizará un mínimo de 20 horas anuales de formación. Contenidos formativos Acogida, adaptación, protección infantil, primeros auxilios, alergias, prevención de riesgos, atención a la diversidad, coeducación, comedor educativo y comunicación con familias. Jornada Jornada completa. Cómo postular Envía tu CV , titulaciones y certificados de formación y experiencia a: laura@emocional.com pedro@emocional.com belen@emocional.com alejandra@emocional.com carlota.martin@emocional.com Con el asunto: “Infantil - Ibiza” Fecha límite: 1 de junio .

• Tusclasesparticulares

  

  Teletrabajo - Profesor/a Particular - Sin Experiencia

  1 month ago

  Palma

  No se requiere experiencia previa como profesor.

• Crovelis

  

  Clinical Research Associate - USA Relocation - palma de mallorca

  7 hours ago

  Palma

  🇺🇸 Clinical Research Associate (CRA) – USA Relocation Opportunity CROVELIS is currently looking for experienced Clinical Research Associates (CRAs) interested in relocating to the United States for a long-term international clinical research assignment. This position offers the opportunity to join a global clinical operations team supporting high-impact international studies in a fast-paced and highly collaborative environment. Selected candidates will relocate to the US for an estimated period of 2–3 years, with relocation and visa support provided by the company. 📍 Location: United States ✈️ Visa & relocation support included 🕒 Long-term assignment (2–3 years) 🔎 What are we looking for? • Minimum 4 years of experience as a CRA in clinical trial monitoring, • Strong experience performing:, • • Site Selection Visits (SSV), • • Site Initiation Visits (SIV), • • Routine Monitoring Visits (RMV), • • Close-Out Visits (COV), • Solid understanding of ICH-GCP, FDA regulations, and clinical operations processes, • Experience managing investigative sites independently and ensuring protocol compliance, • Ability to work in dynamic, fast-paced, and international environments, • Strong communication, organizational, and stakeholder management skills, • Previous exposure to multicountry/global clinical trials is highly valued, • Fluent English level required 💼 Key Responsibilities As a CRA, you will play a critical role in the successful execution of international clinical trials across multiple sites in the United States. Responsibilities will include: • Overseeing site performance and ensuring studies are conducted according to protocol, GCP, SOPs, and regulatory requirements, • Conducting site qualification, initiation, routine monitoring, and close-out visits, • Building strong relationships with investigators, coordinators, and site staff, • Ensuring patient safety, data integrity, and overall study quality throughout the trial lifecycle, • Reviewing source documentation, identifying protocol deviations, and supporting issue resolution, • Collaborating closely with Clinical Trial Managers, vendors, sponsors, and cross-functional teams, • Supporting site activation, enrollment, and retention strategies, • Maintaining accurate and timely study documentation and monitoring reports, • Participating in investigator meetings, trainings, and study planning activities 🚀 Why join CROVELIS? CROVELIS is building a globally focused internal CRO designed to deliver high-quality clinical trial execution through agility, collaboration, and innovation. This role offers a unique opportunity to combine: ✅ International relocation to the US ✅ Career growth within global clinical operations ✅ Exposure to complex and high-visibility studies ✅ Multicultural and collaborative environment ✅ Long-term international experience If you are looking to take your CRA career to an international level and be part of a growing global organization, we would love to hear from you.

• Crovelis

  

  Clinical Research Associate - USA Relocation

  7 hours ago

  Palma

  🇺🇸 Clinical Research Associate (CRA) – USA Relocation Opportunity CROVELIS is currently looking for experienced Clinical Research Associates (CRAs) interested in relocating to the United States for a long-term international clinical research assignment. This position offers the opportunity to join a global clinical operations team supporting high-impact international studies in a fast-paced and highly collaborative environment. Selected candidates will relocate to the US for an estimated period of 2–3 years, with relocation and visa support provided by the company. 📍 Location: United States ✈️ Visa & relocation support included 🕒 Long-term assignment (2–3 years) 🔎 What are we looking for? • Minimum 4 years of experience as a CRA in clinical trial monitoring, • Strong experience performing:, • • Site Selection Visits (SSV), • • Site Initiation Visits (SIV), • • Routine Monitoring Visits (RMV), • • Close-Out Visits (COV), • Solid understanding of ICH-GCP, FDA regulations, and clinical operations processes, • Experience managing investigative sites independently and ensuring protocol compliance, • Ability to work in dynamic, fast-paced, and international environments, • Strong communication, organizational, and stakeholder management skills, • Previous exposure to multicountry/global clinical trials is highly valued, • Fluent English level required 💼 Key Responsibilities As a CRA, you will play a critical role in the successful execution of international clinical trials across multiple sites in the United States. Responsibilities will include: • Overseeing site performance and ensuring studies are conducted according to protocol, GCP, SOPs, and regulatory requirements, • Conducting site qualification, initiation, routine monitoring, and close-out visits, • Building strong relationships with investigators, coordinators, and site staff, • Ensuring patient safety, data integrity, and overall study quality throughout the trial lifecycle, • Reviewing source documentation, identifying protocol deviations, and supporting issue resolution, • Collaborating closely with Clinical Trial Managers, vendors, sponsors, and cross-functional teams, • Supporting site activation, enrollment, and retention strategies, • Maintaining accurate and timely study documentation and monitoring reports, • Participating in investigator meetings, trainings, and study planning activities 🚀 Why join CROVELIS? CROVELIS is building a globally focused internal CRO designed to deliver high-quality clinical trial execution through agility, collaboration, and innovation. This role offers a unique opportunity to combine: ✅ International relocation to the US ✅ Career growth within global clinical operations ✅ Exposure to complex and high-visibility studies ✅ Multicultural and collaborative environment ✅ Long-term international experience If you are looking to take your CRA career to an international level and be part of a growing global organization, we would love to hear from you.

• Crovelis

  

  Clinical Research Associate - USA Relocation - Crovelis

  7 hours ago

  Palma

  🇺🇸 Clinical Research Associate (CRA) – USA Relocation Opportunity CROVELIS is currently looking for experienced Clinical Research Associates (CRAs) interested in relocating to the United States for a long-term international clinical research assignment. This position offers the opportunity to join a global clinical operations team supporting high-impact international studies in a fast-paced and highly collaborative environment. Selected candidates will relocate to the US for an estimated period of 2–3 years, with relocation and visa support provided by the company. 📍 Location: United States ✈️ Visa & relocation support included 🕒 Long-term assignment (2–3 years) 🔎 What are we looking for? • Minimum 4 years of experience as a CRA in clinical trial monitoring, • Strong experience performing:, • • Site Selection Visits (SSV), • • Site Initiation Visits (SIV), • • Routine Monitoring Visits (RMV), • • Close-Out Visits (COV), • Solid understanding of ICH-GCP, FDA regulations, and clinical operations processes, • Experience managing investigative sites independently and ensuring protocol compliance, • Ability to work in dynamic, fast-paced, and international environments, • Strong communication, organizational, and stakeholder management skills, • Previous exposure to multicountry/global clinical trials is highly valued, • Fluent English level required 💼 Key Responsibilities As a CRA, you will play a critical role in the successful execution of international clinical trials across multiple sites in the United States. Responsibilities will include: • Overseeing site performance and ensuring studies are conducted according to protocol, GCP, SOPs, and regulatory requirements, • Conducting site qualification, initiation, routine monitoring, and close-out visits, • Building strong relationships with investigators, coordinators, and site staff, • Ensuring patient safety, data integrity, and overall study quality throughout the trial lifecycle, • Reviewing source documentation, identifying protocol deviations, and supporting issue resolution, • Collaborating closely with Clinical Trial Managers, vendors, sponsors, and cross-functional teams, • Supporting site activation, enrollment, and retention strategies, • Maintaining accurate and timely study documentation and monitoring reports, • Participating in investigator meetings, trainings, and study planning activities 🚀 Why join CROVELIS? CROVELIS is building a globally focused internal CRO designed to deliver high-quality clinical trial execution through agility, collaboration, and innovation. This role offers a unique opportunity to combine: ✅ International relocation to the US ✅ Career growth within global clinical operations ✅ Exposure to complex and high-visibility studies ✅ Multicultural and collaborative environment ✅ Long-term international experience If you are looking to take your CRA career to an international level and be part of a growing global organization, we would love to hear from you.