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...
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 jo...
Si eres un profesional que sabe que tiene los conocimientos y no consigues empleo en el área en que te especializaste y estás seguro que le puedes prestar un servicio a las empresas y/o profesionales de otras áreas la siguiente información te interesa. estás pendiente de las redes sociales, envías hojas de vida sin resultados y/o te han calificado como sobrevalorado por tus conocimientos o te descalifican por tu edad, entonces es tiempo de pensar en tener tu propio negocio de consultoría. si estás en alguno de los siguientes grupos: profesionales independientes, freelances, empresarios,emprendedores, diseñador gráfico,programador,coach,doctores,especialista en funnels y automatización de marketing,copywriter,media buyer / traffickerlead generator,closer / vendedor,affiliate manager,launch manager,evergreen manager,content creator,editor de videos,disenador / ilustrador. puedes ser cualquiera de los siguientes tipos de consultores: [wps_lists icon=»arrow-right» icon_color=»#81d742″] consultor de negocio. consultor de marketing. consultor de ventas. consultor financiero. consultor de rrhh. consultor de imagen personal. consultor en nutrición. consultor de compras. consultor deportivo. consultor de otras especialidades. [/wps_lists] tienes la idea pero no sabes como desarrollarla? en el siguiente video conocerás: [wps_lists icon=»arrow-right» icon_color=»#81d742″] los 11 pasos para crear un negocio de consultoría. cómo puedes certificarte como consultor digital. cuales son los pasos para tener un negocio de consultoría digital. cuales son la...
Job title: pharmacovigilance associate job location: bogotá, bogota, colombia job location type: on-site job contract type: permanent job seniority level: home based 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 clini...
**overview**: - as a manager, clinical operations 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** manage a local clinical team effectively, maximising resource use to deliver operational, quality, and fiscal targets whilst ensuring employee engagement, retention and growth. accellacare - oversee personnel, recruitment directives, meeting financial goals, and the overall operations of the clinical research site. coms verify that ctas are performing to icon standards and performance metrics through efficient utilization of our employees and adherence to their metrics. - dedicated people leader for the local clinical operations team that includes cras, ihcras and ctas as determined by the country team size and structure. - provide effective management support through your team to deliver a high performing culture including managing attrition, development and engagement of the operational group - carrying out all relevant people leadership responsibilities including performance assessments, goal setting and development plans. - managing the local clinical operations team by empowering and coaching them to deliver their key objectives. - understand and follow key principl...
Overview as a manager, clinical operations 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 manage a local clinical team effectively, maximising resource use to deliver operational, quality, and fiscal targets whilst ensuring employee engagement, retention and growth. accellacare – oversee personnel, recruitment directives, meeting financial goals, and the overall operations of the clinical research site. coms verify that ctas are performing to icon standards and performance metrics through efficient utilization of our employees and adherence to their metrics. - dedicated people leader for the local clinical operations team that includes cras, ihcras and ctas as determined by the country team size and structure. - provide effective management support through your team to deliver a high performing culture including managing attrition, development and engagement of the operational group - carrying out all relevant people leadership responsibilities including performance assessments, goal setting and development plans. - managing the local clinical operations team by empowering and coaching them to deliver their key objectives. - understand and follow key principles with regard to r...
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...
Si es consultor, trabajador independiente, quiere ingresar al marketing digital, quiere desarrollar un negocio desde casa, o se encuentra buscando trabajo la siguiente información le interesa. internet se ha constituido en una fuente de múltiples posibilidades de ingreso, y en el siguiente evento online encontrará la siguiente información: [wps_lists icon=»arrow-right» icon_color=»#81d742″] incluir productos de marketing digital en su portafolio de servicios a empresas. vender productos de terceros ganando comisiones como afiliados. venta de productos y contenidos propios. comercializar moda con diseños propios. venta de joyería (accesorios y moda) por internet. modelo de negocio de inmobiliarias en internet. el negocio del turismo en internet. venta de productos digitales. [/wps_lists] y 17 oportunidades más. regístrese en el siguiente enlace para participar en el evento gratuito y online:...
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 ski...
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...
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 welcome you to join us on our mission to shape the future of clinical development we are currently seeking a project manager, pcs to join our diverse and dynamic team. icon insights evidence & value (iev) is part of icon plc, a leading global clinical research organization headquartered in dublin, ireland. our group undertakes consultancy projects for international clients in both the pharmaceutical and medical device sectors, supporting late-phase clinical trials. the project manager will work on multiple projects focusing across different areas from market access, health economics, epidemiology & data analytics, health technology assessment & value communications and patient reported outcomes. our team is based in several countries such as us, uk, brazil, canada, germany, france, india, spain. what you will be doing: contribute towards a culture of business excellence with a focus on quality, scope, timelines adding value to the business and exceeding client expectations. participate at the forefront of innovation and drive delivery using your project leadership expertise. deliver successful working relationships with clients cross functional project planning, scheduling, and implementation define project scope, resource requirements and deliverables evaluate and decide on risk mitigation strategies, associated action plan,...
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 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 ...
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 pro...
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 designs....
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 ...
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 designs....
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 insp...
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 sites and the sponsor - conduct all types of site visits, including selection, initiation, routine monitoring, and close-out - ensure site compliance with ich-gcp, sops, and regulations - maintain up-to-date documentation in ctms and etmf systems - support and track site staff training and maintain compliance records - monitor patient safety, ensuring timely and accurate ae/sae/pqc reporting - support subject recruitment and retention efforts at the site level - oversee drug accountability and ensure proper storage, return, or destruction - resolve data queries and drive timely, high-quality data entry - document site progress and escalate risks or issues to the clinical team - assist in tracking site budgets and ensuring timely site payments (as applicable) - collaborating with cross-functional partners including ctas, ltms, and ctms you are: - a graduate with a bachelor’s degree in life sciences or equivalent, or a qualified rn - eligible to work in united states without visa sponsorship - a clinical research professional with 2+ years of on-site monitoring experience in the pharmaceutical or cro industry - experienced across multiple therapeutic areas, including immunology preferred. - proficient in ich-gcp, local regulatory requirements, and clinical systems like ctms and etmf - a clear communicator, ...
Hasta el próximo viernes 30 de noviembre, las personas, colectivos, grupos animalistas y fundaciones interesadas en formar parte del consejo distrital de protección y bienestar animal tienen la posibilidad de participar. la convocatoria la está liderando el instituto distrital de la participación y acción comunal (idpac). hay cuatro vacantes disponibles. los interesados deben inscribirse por correo electrónico, adjuntado los siguientes documentos: [wps_lists icon=»arrow-circle-right» icon_color=»#59d600″] documento de identidad (tamaño al 150%). acta expedida y firmada por los integrantes de las organizaciones, fundaciones, colectivos o grupos donde concede el aval como delegado o delegada. constancia expedida por la alcaldía local, junta de acción comunal, instituciones públicas o privadas que acrediten un año de experiencia y trayectoria en el sector del bienestar y protección de los animales. formulario de inscripción diligenciado para candidatos o candidatas para ser electos como delegados ante el consejo distrital de protección y bienestar animal, este formulario estará disponible en las páginas web del idpac e idpyba. [/wps_lists] correo electrónico: para información de futuras convocatorias y ofertas laborales, los invitamos a seguirnos en las redes sociales en el : comparta la información utilizando los botones de las redes sociales....
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 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 r...
Pharmacovigilance assistant ii 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 assistant ii to join our diverse and dynamic team. as a pharmacovigilance assistant ii at icon, you will play a critical role in ensuring the accurate collection, processing, and reporting of safety data for clinical trials and marketed products. you will contribute to compliance with global regulatory requirements and help safeguard patient safety in ongoing research and post-marketing activities. locations: colombia sao paolo, brazil what you will be doing: overseeing the collection, processing, and timely reporting of adverse event reports in compliance with regulatory requirements. ensuring accurate data entry and maintenance of pharmacovigilance databases, reviewing reports for consistency and completeness. assisting in the preparation of periodic safety reports, including risk-benefit analyses, for regulatory submissions and sponsors. collaborating with internal teams and external stakeholders to resolve queries related to safety data and pharmacovigilance activities. supporting audit and inspection readiness by maintaining comprehensive documentation of pharmacovigilance activities and safety reports. your profile: bachelor’s degree in life sciences, pharmacy, or a related field. previous experience in pharmacovigilance or drug safety, wi...
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 shape the future of clinical development we are currently seeking a senior clinical data coordinator to join our diverse and dynamic team. as a clinical data coordinator at icon, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. what you will be doing create and maintain detailed data management plans and documentation, ensuring compliance with industry standards and regulatory requirements. participate in the identification and resolution of data discrepancies and issues, working to streamline data flow and enhance data quality throughout the study lifecycle. collaborate closely with cross-functional teams, including clinical operations and biostatistics, to develop and execute data management strategies tailored to specific studies. perform other project activities as required in order to ensure that study timelines are met (for example, filing and archiving of study documentation , dispatching of queries to investigator sites for resolution, etc.). mentor junior data coordinators, providing expert guidance on data reconciliation, coding, and cleaning procedures. your profile bachelor's degree in a relevant field, such as life sciences or healthcare. 3+ years experience in clinical data ...
Patronista senior – moda femenina | style icon colombia patronista senior – moda femenina | style icon colombia marketing | psicología del consumidor | diseño y moda | asesoría de imagen | personal shopper | dirección creativa | relaciones públicas en style icon colombia buscamos una persona talentosa, comprometida y apasionada por el diseño de moda con sentido. queremos sumar a nuestro equipo alguien que entienda la importancia de crear prendas que empoderan, que sepan traducir un diseño en una estructura impecable y que disfruten ser parte de un proceso donde cada detalle tiene alma. • interpretar fichas técnicas y realizar patronaje base y transformaciones. • hacer trazados y cortes con precisión. • apoyar pruebas y ajustes técnicos. • acompañar el proceso de desarrollo desde el diseño hasta la confección final. perfil que buscamos: • manejo sólido de escalado, trazado y conocimientos de telas. • actitud propositiva, responsabilidad y apertura para trabajar en equipo. • pasión por la moda femenina con propósito. • un entorno de trabajo creativo, profesional y con propósito. • posibilidades de crecimiento dentro de una marca en expansión. • estabilidad laboral y participación en el desarrollo de colecciones icónicas. si sientes que esta oportunidad es para ti, envíanos tu hoja de vida. #j-18808-ljbffr...
Project analyst i 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 project analyst i to join our diverse and dynamic team. working closely with our project team, you will provide invaluable guidance and support, ensuring that every task is accomplished with precision and efficiency. you will have the opportunity to collaborate with diverse stakeholders, including clients and vendors, to achieve project objectives and deliverables. your responsibilities: recognizing, exemplifying and adhering to icon's values which centers around our commitment to people, clients and performance. embracing and contributing to a culture of continuous process improvement, streamlining workflows, adding value, and meeting client needs. acting as a key point of contact for assigned clients, gathering project requirements, ensuring smooth project initiation, and managing expectations throughout the project lifecycle. independently managing small to mid-sized translation projects, ensuring alignment with client expectations, timelines, budgets, and quality standards. defining project tasks, monitor progress, track milestones, and proactively managing risks, escalating when necessary. coordinating effectively with internal teams to ensure seamless execution and communication. contributing to internal and client-facing reporting, performance tracking, and issue resol...
As a medical writer, you will join the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence. you will partner with a global pharma company committed to discovering and delivering life-transforming treatments within metabolic disorders, gastroenterology, neurology, inflammation, and oncology. the program is ideal for individuals who thrive in a continually evolving culture within a globally renowned fortune 500 company. the senior medical writer will work with clients and subject matter experts to create, edit, and compile clinical/regulatory marketing documents for new biologics, drugs, or devices, and will direct other medical writers in the writing, editing, and compilation of documents for approval applications. you are: at least 5 years of experience in submission documents during the development phase. global experience with submission documents. a university degree in science or health. strong english skills. experience in client-facing roles. what icon can offer you: our success depends on the quality of our people. that’s why we prioritize building a diverse culture that rewards high performance and nurtures talent. in addition to a competitive salary, icon offers a range of benefits focused on well-being and work-life balance for you and your family. visit our careers website to learn more: https://careers.iconplc.com/benefits at icon, inclusion & belonging are fundamental to our culture. we are committed to providing an inclusive, accessible environment for all candidates and a workplace free of discrimination and...
As a medical writer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. you will be partnering with a global pharma company committed to discovering and delivering life-transforming treatments within metabolic disorders, gastroenterology, neurology, inflammation, as well as oncology. the program is ideal for individuals who thrive in a continually-evolving culture within a globally renowned fortune 500 company. the senior medical writer, working with clients and other subject matter experts, to create, edit, and compile clinical/regulatory marketing for new biologics, drugs, or devices, and to direct other medical writers in the writing, editing and compilation of documents approval applications. you are: at least 5 years of experience in submission documents in the development phase. global experience with submission documents. university degree in science or health. strong english skills. experience in client-facing roles. what icon can offer you: 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 additional benefits. our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. visit our careers website to read more about the benefits of working at icon: https://careers.iconplc.com/benefits...
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 sites and the sponsor conduct all types of site visits, including selection, initiation, routine monitoring, and close-out ensure site compliance with ich-gcp, sops, and regulations maintain up-to-date documentation in ctms and etmf systems support and track site staff training and maintain compliance records monitor patient safety, ensuring timely and accurate ae/sae/pqc reporting support subject recruitment and retention efforts at the site level oversee drug accountability and ensure proper storage, return, or destruction resolve data queries and drive timely, high-quality data entry document site progress and escalate risks or issues to the clinical team assist in tracking site budgets and ensuring timely site payments (as applicable) collaborating with cross-functional partners including ctas, ltms, and ctms you are: a graduate with a bachelor’s degree in life sciences or equivalent, or a qualified rn eligible to work in united states without visa sponsorship a clinical research professional with 2+ years of on-site monitoring experience in the pharmaceutical or cro industry experienced across multiple therapeutic areas, including immunology preferred. proficient in ich-gcp, local regulatory requirements, and clinical systems like ctms and etmf a clear communicator, problem-solver, and collaborative team player willing an...
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...
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 portfol...
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