Project manager, pcs. homebased. mexico, brazil, colombia, 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...
Senior cdc. homebased. mexico 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 sh...
Client services associate ii - homebased - mexico, brazil, chile, colombia, peru, argentina 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 in collaboration with icon, mapi research trust is a non-profit, full-service provider, promoting the use of clinical outcomes assessments (coas) in studies, and encouraging exchanges of patient-centered outcomes (pco) and clinical outcome assessments information among academics, pharmaceutical companies, and health researchers. since the mid-90′s we have been collecting and processing pco information to provide reliable, comprehensive and up-to-date information services. we offer free and subsidized access to clinical outcome assessments information, licensing and their derivatives for thousands of independent and academic research programs in over 130 countries every year, and we maintain the world’s largest library devoted exclusively to coas. through our proqolid & prolabels databases, we create vital links among those at every level of patient-centered outcomes studies. the trust was founded with the mission of centralizing and quickly disseminating reliable, exhaustive questionnaire information to the scientific community. mapi research trust is the largest single coa licensing provider and the most trusted name in distribution of coa instruments exclusively representing over 600 coas. the coa licensing client services asso...
Clinical trial manager 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 are currently seeking a clinical trial manager to join our diverse and dynamic team at icon plc. in this critical role, you will be responsible for overseeing the planning, execution, and successful completion of clinical trials, ensuring adherence to timelines, budgets, and regulatory guidelines. as a leader in our research department, you will collaborate with cross-functional teams, manage site relationships, and provide strategic guidance to drive the successful delivery of clinical trial outcomes. what you will be doing plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards. collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures. build and manage strong relationships with trial investigators and stakeholders. ensure all trials are conducted in compliance with local, national, and international regulations and ethical guidelines. problem-solve and make critical decisions regarding trial design, vendor selection, and risk management. your profile university degree in medicine, science, or equivalent combination of education & experience demonstrated ability to drive the clinical deliverables of a study subject matter expertise in the designated therapeutic area prior monitoring experie...
Overview as a cta you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. you will be partnering with one of the worlds premier biopharmaceutical companies. working across a vast portfolio of medicines and vaccines this company has, over centuries created a strong heritage of delivering innovative treatments and preventive medicines globally. responsibilities what you will be doing: cta assists in the coordination and administration of the study activities from the start up to execution and close out, and within the local study team to ensure quality and consistency of interventional study deliverables to time, cost and quality objectives collects, assists in preparation, reviews and tracks documents for the application process as well as coordination and tracking of study materials and equipment assist in submission of proper application/documents to ec/irb and, where appropriate to regulatory authorities interfaces with investigators, external service providers and cras during the document collection process local administrative main contact and works closely with the cras and/or the lsad for the duration of the study set-up and maintenance of the local etmf and isf including document tracking in accordance with ich-gcp and local requirements ensures essential documents are uploaded in a timely manner to maintain the etmf “inspection readiness” and study documents are ready for final archiving and completion of local part of the etmf and supports the cra in the close out activities for the isf prepar...
Job summary as a cta you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence. you will be partnering with one of the worlds premier biopharmaceutical companies. working across a vast portfolio of medicines and vaccines this company has, over centuries created a strong heritage of delivering innovative treatments and preventive medicines globally responsibilities - collects, assists in preparation, reviews and tracks documents for the application process as well as coordination and tracking of study materials and equipment - assist in submission of proper application/documents to ec/irb and, where appropriate to regulatory authorities - interfaces with investigators, external service providers and cras during the document collection process - local administrative main contact and works closely with the cras and/or the lsad for the duration of the study qualifications - bachelor's degree in a relevant field of study. - previous experience as study coordinator or any other administrative position. - experience with payments and/or invoices and interested in working in payment-related tasks. - excellent planning/ organizational skills - problem solving attitude - strong team player - all employees must read, write and speak fluent english and host country language. benefits our success depends on the quality of our people. that's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. in addition to your competitive salary, icon offers a range of ad...
Client services associate ii - homebased - mexico, brazil, chile, colombia, peru, argentina 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 in collaboration with icon, mapi research trust is a non-profit, full-service provider, promoting the use of clinical outcomes assessments (coas) in studies, and encouraging exchanges of patient-centered outcomes (pco) and clinical outcome assessments information among academics, pharmaceutical companies, and health researchers. since the mid-90′s we have been collecting and processing pco information to provide reliable, comprehensive and up-to-date information services. we offer free and subsidized access to clinical outcome assessments information, licensing and their derivatives for thousands of independent and academic research programs in over 130 countries every year, and we maintain the world’s largest library devoted exclusively to coas. through our proqolid & prolabels databases, we create vital links among those at every level of patient-centered outcomes studies. the trust was founded with the mission of centralizing and quickly disseminating reliable, exhaustive questionnaire information to the scientific community. mapi research trust is the largest single coa licensing provider and the most trusted name in distribution of coa instruments exclusively representing over 600 coas. the coa licensing client service...
About bad marketing: we're a team of 170+ passionate leaders and creatives who have worked diligently to make bad marketing one of the largest and most robust growth marketing agencies in the world. at the core of our philosophy is the belief that excellence stems from a united team working toward a common objective: to not only help our clients grow profitably but also to provide them with an experience they can’t find anywhere else. we specialize in local lead generation, e-commerce, and information marketing; catering to clients that span from auto and local shop owners, to online consumer product brand owners, online gurus selling courses or coaching, and more. our approach to success involves more than just b old a nd d isruptive strategies. we invest in our team through extensive training, continuous support for growth and learning, and the cultivation of a happy and confident company culture. for us, finding fulfillment in your career is just as crucial as excelling in it. about this position: as an email & sms designer, you will play an important role in creating captivating email and sms campaigns, delivering visual messaging and optimize email designs for optimal ctr and conversions. you will be responsible for staying on brand with each client by using the correct fonts, colors, and visuals provided by each client’s branding guidelines. responsibilities: - create compelling and high converting graphic designs for email marketing campaigns. - design and design and develop email templates including icon/ui creation and gifs. - a/b test your...
Pharmacovigilance associate (case processing, colombia) page is loaded pharmacovigilance associate (case processing, colombia) apply remote type office or home locations colombia, bogota time type full time posted on posted 2 days ago job requisition id jr133549 pharmacovigilance associate (case processing, 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 welcome you to join us on our mission to shape the future of clinical development we are currently seeking a pharmacovigilance associate to join our diverse and dynamic team. as a pharmacovigilance associate at icon, you will play a vital role in monitoring and ensuring the safety of pharmaceutical products by collecting, analyzing, and reporting adverse event information. your attention to detail and understanding of regulatory requirements will be essential in supporting the organization’s commitment to patient safety and compliance. what you will be doing: - collecting and reviewing adverse event reports to ensure accurate and timely reporting in accordance with regulatory guidelines. - conducting signal detection and risk assessment activities to identify potential safety issues. - collaborating with cross-functional teams to support safety-related inquiries and investigations. - maintaining up-to-date knowledge of pharmacovigilance regulations and industry best practices. - assisting in the preparation of safety reports and regulatory submissions. your profile: - bachelor's ...
As a cta you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. you will be partnering with one of the worlds premier biopharmaceutical companies. working across a vast portfolio of medicines and vaccines this company has, over centuries created a strong heritage of delivering innovative treatments and preventive medicines globally. what you will be doing: cta assists in the coordination and administration of the study activities from the start up to execution and close out, and within the local study team to ensure quality and consistency of interventional study deliverables to time, cost and quality objectives collects, assists in preparation, reviews and tracks documents for the application process as well as coordination and tracking of study materials and equipment assist in submission of proper application/documents to ec/irb and, where appropriate to regulatory authorities interfaces with investigators, external service providers and cras during the document collection process local administrative main contact and works closely with the cras and/or the lsad for the duration of the study set-up and maintenance of the local etmf and isf including document tracking in accordance with ich-gcp and local requirements ensures essential documents are uploaded in a timely manner to maintain the etmf “inspection readiness” and study documents are ready for final archiving and completion of local part of the etmf and supports the cra in the close out activities for the ...
Overview as a cta you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. you will be partnering with one of the worlds premier biopharmaceutical companies. working across a vast portfolio of medicines and vaccines this company has, over centuries created a strong heritage of delivering innovative treatments and preventive medicines globally responsibilities what you will be doing: cta assists in the coordination and administration of the study activities from the start up to execution and close out, and within the local study team to ensure quality and consistency of interventional study deliverables to time, cost and quality objectives - collects, assists in preparation, reviews and tracks documents for the application process as well as coordination and tracking of study materials and equipment - assist in submission of proper application/documents to ec/irb and, where appropriate to regulatory authorities - interfaces with investigators, external service providers and cras during the document collection process - local administrative main contact and works closely with the cras and/or the lsad for the duration of the study - set-up and maintenance of the local etmf and isf including document tracking in accordance with ich-gcp and local requirements - ensures essential documents are uploaded in a timely manner to maintain the etmf “inspection readiness” and study documents are ready for final archiving and completion of local part of the etmf and supports the cra in the close out activit...
Senior drug safety associate - homebased in switzerland only as a senior drug safety associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. the role is dedicated to an innovative pharma that currently develops and manufactures prescription biopharmaceutical medications in multiple therapeutic areas including oncology, inflammation, and autoimmunity. the senior drug safety associate will be responsible for processing and oversight of adverse event/drug experience reports (serious and non-serious) and other safety related data for marketed products and clinical trials. the position will be responsible for leading case management lifecycle from receipt through case completion. what you will be doing: perform processing and oversight of adverse event/drug experience reports (serious and non-serious) and other safety related data for marketed products and clinical trials. completion of the case management lifecycle including but not limited to: intake, triage, book-in, data entry, peer/quality review, follow-up and submissions. perform case processing (including case deactivations) and data gathering tasks within argus safety database and other systems (i.e. edc systems). assist with literature review and article procurement as required. perform retrospective quality review and document findings, and contribute to metric compilation assist with business partner and other query management. represent pharmacovigilance on project teams. assist with capa/audit or inspection finding investigations a...
Pharmacovigilance associate (case processing, colombia) page is loaded pharmacovigilance associate (case processing, colombia) apply remote type office or home locations colombia, bogota time type full time posted on posted 2 days ago job requisition id jr133549 pharmacovigilance associate (case processing, 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 welcome you to join us on our mission to shape the future of clinical development we are currently seeking a pharmacovigilance associate to join our diverse and dynamic team. as a pharmacovigilance associate at icon, you will play a vital role in monitoring and ensuring the safety of pharmaceutical products by collecting, analyzing, and reporting adverse event information. your attention to detail and understanding of regulatory requirements will be essential in supporting the organization’s commitment to patient safety and compliance. what you will be doing: collecting and reviewing adverse event reports to ensure accurate and timely reporting in accordance with regulatory guidelines. conducting signal detection and risk assessment activities to identify potential safety issues. collaborating with cross-functional teams to support safety-related inquiries and investigations. maintaining up-to-date knowledge of pharmacovigilance regulations and industry best practices. assisting in the preparation of safety reports and regulatory submissions. your profile: bachelor's degree in life scien...
Pharmacovigilance associate (case processing, 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 welcome you to join us on our mission to shape the future of clinical development. we are currently seeking a pharmacovigilance associate to join our diverse and dynamic team. as a pharmacovigilance associate at icon, you will play a vital role in monitoring and ensuring the safety of pharmaceutical products by collecting, analyzing, and reporting adverse event information. your attention to detail and understanding of regulatory requirements will be essential in supporting the organization’s commitment to patient safety and compliance. what you will be doing: collecting and reviewing adverse event reports to ensure accurate and timely reporting in accordance with regulatory guidelines. conducting signal detection and risk assessment activities to identify potential safety issues. collaborating with cross-functional teams to support safety-related inquiries and investigations. maintaining up-to-date knowledge of pharmacovigilance regulations and industry best practices. assisting in the preparation of safety reports and regulatory submissions. your profile: bachelor's degree in life sciences, pharmacy, or a related field; advanced degree preferred. experience in pharmacovigilance, drug safety, or a related area, preferably within a clinical or pharmaceutical environment. strong analytical skills with attention to detail in data collection and re...
Tienes wifi y sabes utilizar tu computador, entonces puedes ganar dinero desde casa. el marketing digital es una opción real para trabajar desde casa y ganar dinero . si en este momento te sientes identificado con una de las siguientes situaciones: [wps_lists icon=»arrow-right» icon_color=»#81d742″] tienes más de 40 años y no consigues empleo? tienes un grupo de amigos y contactos, y te gustaría poder venderles algún producto pero no sabes cuál? tienes una idea de negocio y no sabes por donde comenzar? quieres promocionar tu propia idea de negocio y no sabes como hacerlo? te gustaría comercializar productos de china en redes sociales? quieres vender tus productos durante la temporada de fin de año? quieres vender productos digitales sin tener productos propios? te interesa el tema pero consideras que hay un exceso de información y no sabes por donde comenzar? quieres prepararte en marketing digital como opción complementaria de formación? quieres tener una fuente de ingreso complementaria o principal? te gustaría poder recibir un acompañamiento en marketing digital en el que puedas hacer todas las preguntas que tengas? [/wps_lists] cierre de inscripciones: 30 de noviembre si la respuesta a alguna de las preguntas anteriores es si, te invito a ver el siguiente video:...
Join to apply for the cta. payments role at icon strategic solutions 2 days ago be among the first 25 applicants join to apply for the cta. payments role at icon strategic solutions as a cta you will be joining the world’s largest & most comprehensiv...
As a clinical research associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. what you will be doing: serve as the primary point of contact between investigational si...
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