As a graduate pharmacovigilance associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. you will be partnering with a pharmaceutical company committed to discovering a...
Site activation lead. homebased. mexico, brazil, peru, chile and colombia icon plc is a world-leading healthcare intelligence and clinical research organization. we’re proud to foster an inclusive environment driving innovation and excellence, and we...
Senior project manager - homebased - mexico, colombia, brazil, chile and peru icon plc is a world-leading healthcare intelligence and clinical research organization. we're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development as a senior project manager in icon's language services department, you will lead complex translation and localization projects for pharmaceutical and clinical clients, ensuring seamless execution, high quality, and regulatory compliance. acting as a trusted advisor and subject matter expert, you will manage client relationships, optimize workflows, and drive continuous improvement. you will also play a key role in mentoring others, solving complex challenges, and contributing to strategic initiatives that support the growth and integration of icon's language services. what you will be doing: recognizing, exemplifying and adhering to icon's values which centres around our commitment to people, clients and performance. as a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs. maintaining and sharing awareness of pharma/biotech/medical device trends and evolving client expectations. independently managing complex, high-value translation and localization projects from initiation through delivery. acting as the primary client partner, ensuring clear communication,...
**importante el ingles!** artists at play empresa de contenidos grabados, licencias y gestión para artistas musicales. creadores de contenido gráfico, visual y publicitario para los mismos artistas con los que trabajamos, sello discografico asesor hotelero/marketing airbnb **requisitos**: **nivel de ingles avanzado o intermedio** - gestiones y soluciones de huespedes y hospedaje en hotel (icon suites) que hace parte del jefe a cargo de artists at play. - cuidar de los huespedes, asesorar e informar con cautela las normas y reglas del hotel en su instancia. tipo de puesto: tiempo completo tipo de puesto: tiempo completo...
Empresa de hoteleria, hostal y entretenimiento icon suites, necesita un equipo de trabajo de obreros de construccion para finalizar un proyecto pausado. objetivo: preparar terrenos de **construcción**, cavar zanjas, colocar refuerzos en las paredes laterales de las excavaciones, construir andamios y limpiar escombros, restos, y otros materiales de desecho. pueden ayudar a trabajadores en otros oficios de la **construcción**. **requisitos**: contar con su estricto equipo de trabajo de soluciones con respecto a lo indicado. lunes a viernes tipo de puesto: tiempo completo...
El hotel icon suites solicida para su equipo de trabajo portero en puerta para el control de la entrada de huespedes y personal de trabajo - **requisitos**:_ buena precencia actitud caracter fuerte experiência en el area (1 año) obligaciones: - prestar atencion y tener en cuenta todo el personal que entra y sale del edifico, ser conciente de quien sale y quien entra - tener buena memoria para reconocer personas - buena requisa al personal tanto en la entrada como la salida - ningun personal te le permite entrar con ninguna clase de arma, decomisarla en el acto. - ser cordial y amable y muy atento horarios lunes a domingo (dias rotativos y horas rotativas) habran dias que no se laborara. tipo de puesto: tiempo completo...
Senior project manager - homebased - mexico, colombia, brazil, chile and peru icon plc is a world-leading healthcare intelligence and clinical research organization. we’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. as a senior project manager in icon’s language services department, you will lead complex translation and localization projects for pharmaceutical and clinical clients, ensuring seamless execution, high quality, and regulatory compliance. acting as a trusted advisor and subject matter expert, you will manage client relationships, optimize workflows, and drive continuous improvement. you will also play a key role in mentoring others, solving complex challenges, and contributing to strategic initiatives that support the growth and integration of icon’s language services. what you will be doing: - recognizing, exemplifying, and adhering to icon's values centered around our commitment to people, clients, and performance. - contributing to our culture of process improvement by streamlining processes, adding value, and meeting client needs. - keeping abreast of pharma/biotech/medical device trends and evolving client expectations. - managing complex, high-value translation and localization projects from start to finish. - serving as the primary client partner, ensuring clear communication, managing expectations, and providing strategic guidance. - advising clients and internal teams as a subject matter expert in life science...
Empresa de hotelería, hostal y entretenimiento icon suites, necesita un equipo de trabajo de obreros de construcción para finalizar proyectos pausado. objetivo: preparar terrenos de **construcción**, cavar zanjas, colocar refuerzos en las paredes laterales de las excavaciones, construir andamios y limpiar escombros, restos, y otros materiales de desecho. pueden ayudar a trabajadores en otros oficios de la **construcción**. **requisitos**: contar con su estricto equipo de trabajo de soluciones con respecto a lo indicado. lunes a viernes 8:00 am - 5:00 pm tipo de puesto: tiempo completo...
Empresa de hoteleria, hostal y entretenimiento icon suites, necesita un equipo de trabajo de obreros de construccion para finalizar un proyecto pausado. objetivo: preparar terrenos de **construcción**, cavar zanjas, colocar refuerzos en las paredes laterales de las excavaciones, construir andamios y limpiar escombros, restos, y otros materiales de desecho. pueden ayudar a trabajadores en otros oficios de la **construcción**. **requisitos**: contar con su estricto equipo de trabajo de soluciones con respecto a lo indicado. tipo de puesto: tiempo completo...
Empresa de hotelería, hostal y entretenimiento icon suites, necesita un equipo de trabajo de obreros de construcción para finalizar proyectos pausado. objetivo: preparar terrenos de construcción, cavar zanjas, colocar refuerzos en las paredes laterales de las excavaciones, construir andamios y limpiar escombros, restos, y otros materiales de desecho. pueden ayudar a trabajadores en otros oficios de la construcción. requisitos: contar con su estricto equipo de trabajo de soluciones con respecto a lo indicado. lunes a viernes 8:00 am 5:00 pm tipo de puesto: tiempo completo...
As clinical research associate (cra), you will be joining the world's largest & most comprehensive clinical research organization, powered by healthcare intelligence. a cra is a professional who contributes to accelerated drug/device/outcomes research through independent monitoring of studies to ensure patient safety and data integrity. you will be partnering with one of our global pharmaceutical clients; a science-based company with one of the most exciting product pipelines in the industry. this global pharmaceutical client develops breakthrough innovative medicines to improve and extend the opportunity to build your career in a rewarding customer-focused environment that supports creativity, collaboration and performance. **what you will be doing**: - completes onsite and remote monitoring activities in accordance with all ich-gcp guidelines, applicable regulations, sops and study processes - verifies the protection of study participants by confirming informed consent procedures and protocol have been performed in accordance to applicable regulations. - ensures the integrity of clinical data and that the study is conducted in compliance with approved protocol, gcp, applicable regulations and sops. - writes and submits reports of investigational site findings and updates applicable tracking systems. escalates observed deficiencies, issues, and corrective and preventative action plans as appropriate. - participates in audit preparation and follow-up activities as needed. - may serve as preceptor, providing training to less experienced clinical team members. -...
**intercompany specialist** bogotá, colombia en dhl global forwarding, las personas son lo más importante. por eso nuestro objetivo es atraer y retener el mejor talento alrededor del mundo. nos encontramos en la búsqueda de nuestro próximo intercompany specialist. **tu objetivo serÁ**: apoyar de manera eficiente y oportuna la gestión operativa y analítica del proceso intercompany (partners dhl), con el fin de garantizar la integridad y exactitud de las cifras contenidas en los estados financieros conforme a las normas aplicables en colombia, las políticas contables corporativas y controles internos asociados. el especialista de intercompañías es responsable de la gestión y ejecución eficiente del proceso de principio a fin de intercompañías para garantizar el cumplimiento de los acuerdos de nível de servicio, incluyendo la gestión y/o ejecución de procesos financieros fundamentales. revisa, desarrolla, documenta, implementa y gestiona procesos y controles y sistemas contables para garantizar un nível adecuado de proceso y resultado. trabaja de manera colaborativa con los diferentes equipos para lograr mejoras en el proceso. **tus principales responsabilidades**: - revisa y envía información para el registro de asientos contables para transacciones y garantiza la precisión del libro mayor de las cuentas de ic. - revisión y gestión del reconocimiento de los gastos intercompany mensuales (ic-doe), control de tareas de la sub-región cenac - ejecutar y gestionar los controles icon de rtr-ic establecidos a nível global y aplicables para dgf co acorde lineamientos reg...
As a cra you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. a cra is a professional who contributes to accelerated drug/device/outcomes research through independent monitoring of studies to ensure patient safety and data integrity. you will have an opportunity to work in a solid partnership and an environment driven by innovation and continuous improvement. this program is for you if you are looking for an environment where people feel they belong and are empowered to reach their full potential, perform at their best and make a valued contribution to saving lives. **what you will be doing**: - completes onsite and remote monitoring activities in accordance with all ich-gcp guidelines, applicable regulations, sops and study processes. - verifies the protection of study participants by confirming informed consent procedures and protocol have been performed in accordance to applicable regulations. - ensures the integrity of clinical data and that the study is conducted in compliance with approved protocol, gcp, applicable regulations and sops. - writes and submits reports of investigational site findings and updates applicable tracking systems. escalates observed deficiencies, issues, and corrective and preventative action plans as appropriate. - participates in audit preparation and follow-up activities as needed. - may serve as preceptor, providing training to less experienced clinical team members. - may be assigned clinical tasks where advanced negotiating skills are required. **y...
Icon plc is a world-leading healthcare intelligence and clinical research organization. from molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations. with our patients at the center of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. our people are our greatest strength, are at the core of our culture, and the driving force behind our success. icon people have a mission to succeed and a passion that ensures what we do, we do well. we have an incredible opportunity for a **senior** **clinical data lead** to join the team. **location**: home-based or office-based - mexico - colombia **overview of the role**: as a senior clinical data lead you will be the point of contact for day to day activity on a study with key responsibilities for study set-up and close-out tasks as well as overseeing and coordinating tasks delegated to the study team members both locally and in other offices. you will also co-ordinate with data management teams, studies and programs of studies and independently oversee the performance of data management activities on multiple studies. - independently prepare all materials and take part in study kick off (internal and external) meeting. - review all activity on an ongoing basis to identify out of scope tasks and bring to the attention of the dmpm and contract analyst. - lead the development of specifications, implementation, and testing for the ecrf o...
Icon plc is a world-leading healthcare intelligence and clinical research organization. we’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. we offer challenging work in a respectful and friendly global working environment surrounded by a world of innovation driven mindsets and practices. in addition, learning and development for all employees is key, because your growth is our growth. **what you will be doing**: - engage with internal and external stakeholders around medical/scientific topics to advance understanding of the disease, pharmaceutical product or medical devices. - attends and follows up on scientific congresses, symposia, and other medical events. - delivers scientific presentations and education to hcp and facilitate of best practice scientific exchange. - informs stakeholders on safety issues - identifies potential speakers, detractors, opinion leaders and engage with them - as appropriate, support design and development of clinical trials initiated by investigators. - evaluate, review and propose, when and where appropriate, revisions to protocols in support of the development and/or medical strategies of the assigned product(s). - undertake the necessary revisions to protocols, ensuring full compliance with all established procedures and guidelines, as well as appropriate communication to other involved/impacted colleagues and/or external parties. - support clinical operations providing medical and scientific information at i...
Senior project manager - homebased - mexico, colombia, brazil, chile and peru icon plc is a world-leading healthcare intelligence and clinical research organization. we’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. as a senior project manager in icon’s language services department, you will lead complex translation and localization projects for pharmaceutical and clinical clients, ensuring seamless execution, high quality, and regulatory compliance. acting as a trusted advisor and subject matter expert, you will manage client relationships, optimize workflows, and drive continuous improvement. you will also play a key role in mentoring others, solving complex challenges, and contributing to strategic initiatives that support the growth and integration of icon’s language services. what you will be doing: - recognizing, exemplifying, and adhering to icon's values centered around our commitment to people, clients, and performance. - contributing to our culture of process improvement by streamlining processes, adding value, and meeting client needs. - keeping abreast of pharma/biotech/medical device trends and evolving client expectations. - managing complex, high-value translation and localization projects from start to finish. - serving as the primary client partner, ensuring clear communication, managing expectations, and providing strategic guidance. - advising clients and internal teams as a subject matter expert in life science...
Empresa de hoteleria, hostal y entretenimiento icon suites, necesita un equipo de trabajo de obreros de construccion para finalizar un proyecto pausado. objetivo: preparar terrenos de **construcción**, cavar zanjas, colocar refuerzos en las paredes laterales de las excavaciones, construir andamios y limpiar escombros, restos, y otros materiales de desecho. pueden ayudar a trabajadores en otros oficios de la **construcción**. **requisitos**: contar con su estricto equipo de trabajo de soluciones con respecto a lo indicado. tipo de puesto: tiempo completo...
As a cra you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. a cra is a professional who contributes to accelerated drug/device/outcomes research through independent monitoring of studies to ensure patient safety and data integrity. you will have an opportunity to work in a solid partnership and an environment driven by innovation and continuous improvement. this program is for you if you are looking for an environment where people feel they belong and are empowered to reach their full potential, perform at their best and make a valued contribution to saving lives. **what you will be doing**: - completes onsite and remote monitoring activities in accordance with all ich-gcp guidelines, applicable regulations, sops and study processes. - verifies the protection of study participants by confirming informed consent procedures and protocol have been performed in accordance to applicable regulations. - ensures the integrity of clinical data and that the study is conducted in compliance with approved protocol, gcp, applicable regulations and sops. - writes and submits reports of investigational site findings and updates applicable tracking systems. escalates observed deficiencies, issues, and corrective and preventative action plans as appropriate. - participates in audit preparation and follow-up activities as needed. - may serve as preceptor, providing training to less experienced clinical team members. - may be assigned clinical tasks where advanced negotiating skills are required. **y...
Icon plc is a world-leading healthcare intelligence and clinical research organization. we’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. we offer challenging work in a respectful and friendly global working environment surrounded by a world of innovation driven mindsets and practices. in addition, learning and development for all employees is key, because your growth is our growth. **what you will be doing**: - engage with internal and external stakeholders around medical/scientific topics to advance understanding of the disease, pharmaceutical product or medical devices. - attends and follows up on scientific congresses, symposia, and other medical events. - delivers scientific presentations and education to hcp and facilitate of best practice scientific exchange. - informs stakeholders on safety issues - identifies potential speakers, detractors, opinion leaders and engage with them - as appropriate, support design and development of clinical trials initiated by investigators. - evaluate, review and propose, when and where appropriate, revisions to protocols in support of the development and/or medical strategies of the assigned product(s). - undertake the necessary revisions to protocols, ensuring full compliance with all established procedures and guidelines, as well as appropriate communication to other involved/impacted colleagues and/or external parties. - support clinical operations providing medical and scientific information at i...
As country study manager (csm), you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence. you will be partnering with a pharmaceutical company committed to discovering and developing treatments that improve and save people´s lives. working in this program you will feel challenged and supported to advance in your professional career while making a truly impact. - **what you will be doing**: - planning, management, and oversight of clinical study execution in accordance with the global program strategy, through leadership of the cross-functional local study team (lst). - contributes and develops to program/study-specific materials - e.g., monitoring plan, study specific training documents. - accountable for site-level goal setting and study-specific deliverables for clinical sites within their country/-ies. - contributes to, deliver and/or lead cra, investigator and study coordinator training. - provides oversight and monitoring of applicable vendor activities e.g., laboratories and equipment provisioning. - provides country level input into the country operational plan (cop) and partner with the dfm through feasibility and with the gcms to ensure local delivery of the study. - responsible for approval of baseline and revised enrolment plans (country level). - monitors the execution of the clinical study against timelines, deliverables, and budget for that country. - translates global start up requirements into local country targets - monitors and acts upon data flow metrics - review, trend i...
Elevate your career with the hart team!are you ready to launch your career to new heights in an inspiring, forward-thinking environment? at the hart team, we're not just looking to fill a role; we're inviting a transaction coordinator to become a core part of our success story! if you're ambitious, strategic, and eager to make a real impact in the world of real estate, this is your moment. in this role, you'll work directly with our executive team, sparking innovation and helping shape our vision. here, your creativity is celebrated, your growth is prioritized, and every contribution you make is valued. ready to make waves in real estate? let's connect!join our team and make an impact!we handle and close more than 100 transactions each year, keeping up a fast-paced momentum that fuels our team's drive and success!we're a proudly part of exp realty, the top cloud-based real estate brokerage known for innovation, excellence, and expansive market reach. led by wayne hartard, an icon agent ranking in the top 3% out of over 90,000 agents at exp realty, we bring unparalleled expertise and dedication to every client and transaction.the roleyou will be responsible for : oversee a pipeline of 150+ active transaction files, ensuring each file progresses smoothly from start to close.track deadlines, required documentation, and client communications for each transaction, proactively managing any potential delays.responsible for opening all transaction files and creating new listings for properties as they come on the market.build detailed property listings, ensuring accuracy and...
Empresa de hoteleria, hostal y entretenimiento icon suites, necesita un equipo de trabajo de obreros de construccion para finalizar un proyecto pausado. objetivo: preparar terrenos de **construcción**, cavar zanjas, colocar refuerzos en las paredes laterales de las excavaciones, construir andamios y limpiar escombros, restos, y otros materiales de desecho. pueden ayudar a trabajadores en otros oficios de la **construcción**. **requisitos**: contar con su estricto equipo de trabajo de soluciones con respecto a lo indicado. tipo de puesto: tiempo completo tipo de puesto: tiempo completo...
Elevate your career with the hart team!are you ready to launch your career to new heights in an inspiring, forward-thinking environment? at the hart team, we're not just looking to fill a role; we're inviting a transaction coordinator to become a core part of our success story! if you're ambitious, strategic, and eager to make a real impact in the world of real estate, this is your moment. in this role, you'll work directly with our executive team, sparking innovation and helping shape our vision. here, your creativity is celebrated, your growth is prioritized, and every contribution you make is valued. ready to make waves in real estate? let's connect!join our team and make an impact!we handle and close more than 100 transactions each year, keeping up a fast-paced momentum that fuels our team's drive and success!we're a proudly part of exp realty, the top cloud-based real estate brokerage known for innovation, excellence, and expansive market reach. led by wayne hartard, an icon agent ranking in the top 3% out of over 90,000 agents at exp realty, we bring unparalleled expertise and dedication to every client and transaction.the roleyou will be responsible for : be the voice of success: strong verbal and written communication skills that engage and inspire.daily client prospecting: generate new clients every day from a variety of lead sources!respond rapidly: handle all inbound leads from internet sources, sign calls, and beyond.coordinate key appointments: set up appointments for our listing and buyer specialists.master lead management: input, organize and manage cl...
Se espera que todas las personas que trabajan en nrc se acojan a los valores fundamentales de la organización: dedicación, innovación, inclusión y responsabilidad. estas actitudes y creencias guiarán nuestras acciones y relaciones. ¿qué buscamos? el consejo noruego de refugiados (nrc) está en búsqueda de una persona profesional dedicada, resiliente y dinámica para asumir el rol de oficial técnico/a de administración quien tiene como responsabilidad liderar las necesidades de administración de la oficina regional de américa latina. el propósito del cargo es asegurar una correcta gestión interna de la oficina y mejorar la eficiencia de los recursos regionales. ¿cuáles serán tus responsabilidades? asegurar el cumplimiento de las políticas, herramientas, manuales y directrices de nrc. apoyar con la implementación del portafolio de funciones de soporte delegadas según el plan de acción. preparar y elaborar los informes de situación que requiera la dirección. asegurar el correcto archivo de los documentos. promover y compartir ideas para mejorar la función de apoyo. por favor descarga el para saber más sobre la posición. requisitos de educación y experiencia título universitario relevante, por ejemplo, en administración de empresas, logística, contabilidad, recursos humanos. experiencia mínima de trabajo de tres (3) años en cargos similares, preferiblemente en un contexto humanitario, con ong, en un papel de apoyo ejecutivo. experiencia previa de trabajo en contextos complejos y volátiles experiencia comprobable relacionada con las responsabilidades del cargo. nivel medio en el i...
**we are seeking a graphic designer! someone with a good sense of aesthetics, good handle of illustrator and comprehensive knowledge of the countless signage material options.** * responsibilities will include: - confer with clients in order to determine their specific creative requirements. - provide clients with information on designs and sizes. - generate customers’ concepts and ideas into graphics. - ensure that colors and tones are in accordance with clients’ requirements. - perform duties such as symbol and icon creation. - design signs to correct metrics such as shape, size, and color. - review designs, edit and make necessary changes - ensure all assignments are final on time for development * * **requirements**: - advanced english level - proven work experience as a graphic designer with strong editing skills and excellent portfolio - solid experience with digital technology and photo editing software packages - knowledge of 3d rendering, computer imaging, photographic techniques and color composition - creative mind with an eye for detail. - good handle of adobe creative suite. - a can-do attitude: no task is too small or too daunting. - have an eye and interest in good design. - great time management skills, thrives on multitasking (but still have focus for each task) * tipo de puesto: tiempo completo, indefinido salario: $1.600.000 - $2.000.000 al mes pregunta(s) de postulación: - can you commute from 8am to 5pm from monday to friday? idioma: - ingles (deseable)...
Empresa de hoteleria, hostal y entretenimiento icon suites, necesita un equipo de trabajo de obreros de construccion para finalizar un proyecto pausado. objetivo: preparar terrenos de **construcción**, cavar zanjas, colocar refuerzos en las paredes laterales de las excavaciones, construir andamios y limpiar escombros, restos, y otros materiales de desecho. pueden ayudar a trabajadores en otros oficios de la **construcción**. **requisitos**: contar con su estricto equipo de trabajo de soluciones con respecto a lo indicado. tipo de puesto: tiempo completo tipo de puesto: tiempo completo...
As clinical research associate (cra), you will be joining the world's largest & most comprehensive clinical research organization, powered by healthcare intelligence. a cra is a professional who contributes to accelerated drug/device/outcomes research through independent monitoring of studies to ensure patient safety and data integrity. you will be partnering with one of our global pharmaceutical clients; a science-based company with one of the most exciting product pipelines in the industry. this global pharmaceutical client develops breakthrough innovative medicines to improve and extend the opportunity to build your career in a rewarding customer-focused environment that supports creativity, collaboration and performance. **what you will be doing**: - completes onsite and remote monitoring activities in accordance with all ich-gcp guidelines, applicable regulations, sops and study processes - verifies the protection of study participants by confirming informed consent procedures and protocol have been performed in accordance to applicable regulations. - ensures the integrity of clinical data and that the study is conducted in compliance with approved protocol, gcp, applicable regulations and sops. - writes and submits reports of investigational site findings and updates applicable tracking systems. escalates observed deficiencies, issues, and corrective and preventative action plans as appropriate. - participates in audit preparation and follow-up activities as needed. - may serve as preceptor, providing training to less experienced clinical team members. -...
Direct message the job poster from icon management human resources director / hrbp/ human resources manager / talent management / master in human resources management about us! icon management is a dynamic company with a team of exceptional professio...
As a clinical research associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. you will be partnering with one of our global pharmaceutical clients; a company that is ...
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