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...
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...
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,...
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...
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...
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 ...
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...
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...
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 clie...
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 ...
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...
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...
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