Lavori presso Icon plc
Icon plc | Copenhagen
| Medicina, Inglese
“Regular job offer for a Study Start Up Associate II at ICON, a global healthcare research organization. Requires 2+ years in clinical site start-up, regulatory compliance, and site activation. Involves document review, team collaboration, and performance tracking. Competitive benefits and inclusive workplace culture.”
“Regular job offer for Study Start Up Associate II at ICON, a global clinical research organization. Requires 2+ years in clinical site start-up, BS degree, and expertise in essential documents (ICF, FDF, 1572). Involves site activation, compliance, and collaboration with CROs and teams. Competitive benefits and inclusive workplace.”
“Clinical Trial Manager position at ICON, a global healthcare research organization. Remote-based in Porto, Portugal. Requires oncology experience, project management skills, and leadership. Involves coordinating clinical trials, managing budgets, and leading cross-functional teams. Competitive salary, benefits, and career development opportunities included.”
“Contratação para Analista de Contratos I na ICON, empresa global de pesquisa clínica. Função home-based no Brasil, com 2+ anos de experiência em contratos e orçamentos em pesquisa clínica. Salário competitivo, benefícios e pacote de recompensas. Viagens ocasionais (5%). Requisitos: inglês avançado, habilidades analíticas e comunicação.”
Icon plc | Mexico City
| Logistica, Inglese
“Se busca un Global Supply Chain Specialist en ICON para gestionar y optimizar procesos de cadena de suministro en México D.F. Requiere experiencia en logística global, análisis de datos y colaboración con equipos multidisciplinares. Modalidad híbrida. Beneficios incluyen salario competitivo, seguros médicos y planes de desarrollo profesional.”
“12-month contract role in Dublin for a Finance Manager at ICON, a healthcare intelligence and clinical research organization. Hybrid position overseeing financial operations, budgeting, and reporting for clinical projects. Requires ACA/ACCA/CIMA qualification, finance management experience, and strong analytical skills. Offers competitive salary, benefits, and career development opportunities.”
Icon plc | Mexico City
| Medicina, Inglese
“ICON recherche un Associate Project Manager (Laboratory) pour gérer 10-15 études cliniques, assurer la satisfaction client et représenter l'entreprise lors de réunions. Profil : Bac+2 en santé/science, 2 ans d'expérience en recherche clinique ou gestion de projet, anglais courant. Poste en présentiel avec avantages compétitifs.”
“Project Manager, Laboratory role at ICON for home-based work in Mexico. Requires project/program management experience in clinical research, managing 10-15 studies, ensuring GCP compliance, and acting as sponsor liaison. Bachelor's in life sciences/healthcare preferred. Competitive salary, benefits, and career development offered.”
“Senior Clinical Research Coordinator position in Montpellier, France, for a Hypersomnolence study. Requires Bachelor's in life sciences, clinical coordination experience, GCP knowledge, and team leadership. Involves managing sleep disorder patient studies, data collection, and cross-functional coordination with ICON/PPD and sponsor teams.”
“Clinical Associate role at ICON supporting clinical trial design, execution, and monitoring. Requires a relevant bachelor's degree, clinical research experience, and 60% travel. Offers competitive salary, benefits, and career development in a collaborative healthcare CRO environment.”
“Manager, Financial Business Partnering role in Dublin with hybrid work model. Requires ACA/ACCA/CIMA qualification, finance management experience in healthcare/clinical research, and skills in budgeting, financial reporting, and compliance. Competitive salary, benefits, and career development opportunities included.”
“ICON seeks a Clinical Trial Manager for Oncology (Late Development) to lead global clinical studies, ensuring compliance with ICH-GCP and regulatory standards. Role involves operational planning, stakeholder management, and risk mitigation for life-changing therapies. Requires oncology trial experience, Life Sciences degree, and strong communication skills. Home-based in the UK.”
Icon plc | Reading
| Risorse Umane, Inglese
“ICON is hiring a Workday HRIS Lead Specialist (Hybrid/Remote in UK) to oversee HR tech strategy, Workday HCM/Recruiting/Compensation/Absence systems, team leadership, governance, and supplier management. Requires HRIS experience, Workday expertise, and strategic leadership. Competitive salary and benefits included.”
“Full-time Logistics Specialist role in Kyiv, Ukraine for ICON, managing shipments, import/export compliance, and WMS processes. Requires 2+ years in logistics, fluent Ukrainian, upper-intermediate English, and on-site availability. Competitive salary and benefits included.”
“Lead Resource Planning Specialist role at ICON for remote work in Ireland. Oversees resource forecasting, allocation, and utilisation in clinical projects. Requires experience in resource planning, advanced Excel, data analysis, and stakeholder management. Offers competitive salary, benefits, and career development in a healthcare CRO.”
Icon plc | Buenos Aires
| Medicina, Inglese
“Clinical Trial Manager position at ICON for managing day-to-day clinical trial operations, ensuring compliance with regulations, and collaborating with cross-functional teams. Requires experience in clinical trial management, therapeutic expertise, and willingness to travel (25%). Competitive benefits package offered.”
“ICON busca un Clinical Site Associate para apoyar la gestión de sitios clínicos, asegurando el cumplimiento y calidad en ensayos clínicos. Requiere experiencia en investigación clínica o administración, habilidades organizativas y dominio de MS Office. Ofrece salario competitivo, beneficios integrales y oportunidades de desarrollo profesional.”
“Remote role for ICON as a Clinical Study Manager overseeing clinical trials, ensuring regulatory compliance, data integrity, and team collaboration. Requires a scientific degree, clinical trial experience, and strong project management skills. Offers competitive salary, benefits, and career development in healthcare research.”
“ICON seeks a Clinical Trial Coordinator (SMA I) to support site monitoring, ensure GCP compliance, and manage trial documentation. Requires a relevant Bachelor's degree, organizational skills, and willingness to travel (~25%). Competitive salary, benefits, and career development offered.”
Icon plc | Dublin
| Risorse Umane, Inglese
“ICON seeks a Workday HRIS Lead Specialist in Dublin for hybrid office role. Responsible for Workday HRIS operations, governance, team leadership, and configuration management. Requires HR tech experience, strategic alignment, and team management. Competitive salary, benefits, and travel (5%) included.”
“Part-time, site-based Clinical Research Coordinator role in Warsaw, Gdańsk, Łódź, or Zabrze (6-20h/week). Supports oncology project initiatives with data analysis, reporting, and team collaboration. Requires a bachelor's degree in a relevant field and experience in project support. Competitive benefits package offered.”
“Posto de Especialista em Consentimento Informado II na ICON, empresa global de pesquisa clínica. Responsável por desenvolver, revisar e supervisionar documentos de consentimento para ensaios clínicos complexos, garantindo conformidade regulatória e alinhamento com protocolos. Requer experiência em pesquisa clínica, conhecimento em GCP e habilidades de comunicação e gestão de stakeholders.”
“Site Engagement Manager role at ICON for designing and analyzing clinical trials, collaborating with cross-functional teams, and fostering relationships with study sites and investigators to enhance patient recruitment and retention.”
“Oferta de empleo como Study Start-up Associate II en ICON, empresa de investigación clínica. Requiere título universitario y 2+ años de experiencia en activación de sitios clínicos. Incluye salario competitivo, beneficios de salud y desarrollo profesional en un entorno colaborativo y orientado a resultados.”
“ICON seeks a Clinical Registry Coordinator with 4+ years in pharmaceutical/clinical development. Role involves overseeing clinical trial data transparency, managing registries (e.g., clinicaltrials.gov), and ensuring regulatory compliance. Requires project management, vendor coordination, and advanced Microsoft Office skills. Full remote position.”
Icon plc | Livingston
| Medicina, Inglese
“Clinical Research Associate (CRA II) role in Scotland/Northern UK for ICON. Requires 2+ years experience, Bachelor's in scientific/healthcare field, ICH-GCP knowledge, and 60% travel. Responsible for trial monitoring, data integrity, and patient safety. Competitive salary and benefits package offered.”
“Lead Resource Planning Specialist role at ICON for remote work in Romania. Responsible for resource planning, demand forecasting, capacity analysis, and stakeholder management in a global healthcare organization. Requires strong analytical skills, stakeholder management, and experience in resource planning within a matrixed environment.”
“ICON busca un Coordinador de Investigación Clínica para roles presenciales a tiempo parcial. Requiere título universitario en áreas relevantes, 2+ años de experiencia en apoyo de proyectos, preferiblemente en oncología, y habilidades analíticas y de colaboración. Ofrece salario competitivo, beneficios integrales y oportunidades de desarrollo profesional.”
“Clinical Site Associate (Inhouse CRA) role in Ankara for ICON, a clinical research organization. Supports site management, trial compliance, and documentation. Requires life sciences/healthcare degree or equivalent experience. Involves travel (~10%) and collaboration with CRAs. Offers competitive salary, benefits, and career development.”
“ICON seeks a Clinical Trial Associate (CTA) with 1+ years of experience to coordinate and administer clinical trials, ensure regulatory compliance, and support study documentation. Requires a scientific/healthcare degree, fluency in Czech and English, and occasional travel. Offers competitive salary, benefits, and career development in a collaborative healthcare research environment.”
Icon plc | Mexico City
| Medicina, Inglese
“ICON seeks a Medical Affairs Specialist to provide administrative and medical support, review lab reports, monitor protocols, and collaborate with cross-functional teams. Requires life sciences background, clinical research experience, and strong attention to detail. Hybrid role with competitive salary, health benefits, and career development opportunities.”
Icon plc | Dublin
| Risorse Umane, Inglese
“ICON seeks a Workday HRIS Manager to lead HR technology initiatives, optimize Workday systems, and manage a team. Requires 5+ years of Workday experience, HR process expertise, and strong leadership skills. Hybrid role with competitive salary, benefits, and career development opportunities in the UK or Ireland.”
Icon plc | Sao Paulo
| Medicina, Inglese
“Clinical Trial Manager position in Oncology at ICON, managing day-to-day operations, ensuring compliance with regulations, and collaborating with cross-functional teams. Requires experience in clinical trials, therapeutic area expertise, and willingness to travel (25%). Competitive salary and benefits package offered.”
Icon plc | Mexico City
| Medicina, Inglese
“Hybrid Clinical Site Associate role in Mexico City for ICON, a global healthcare research organization. Supports clinical trial site management, document tracking, and compliance. Requires life sciences/healthcare/business degree or equivalent experience. Offers competitive salary, benefits, and career development in a collaborative environment.”
Icon plc | Sao Paulo
| Medicina, Inglese
“Seeking a Clinical Research Associate II (CRA II) in São Paulo, Rio de Janeiro or Porto Alegre to monitor clinical trials, ensure protocol compliance, data integrity, and patient safety. Requires 2+ years of experience, scientific degree, and 60% travel. Competitive salary, benefits, and career development included.”
“Hybrid Clinical Trial Associate role in Bulgaria for ICON, focusing on payments and administrative tasks within clinical trials. Requires a scientific/healthcare degree, 1+ year in payments (preferably in research sites or CRO/Pharma), and knowledge of clinical trial regulations. Involves TMF management, CTMS support, site payments reconciliation, and team coordination.”
Icon plc | Dublin
| Risorse Umane, Inglese
“Lead Specialist role in Dublin for Workday HRIS management at ICON, a global healthcare research organization. Oversees HR technology strategy, Workday HCM/Recruiting/Compensation/Absence operations, team leadership, governance, and supplier coordination. Requires HRIS experience, strategic thinking, and hybrid office work.”
“ICON keres Clinical Research Physician II-t budapesti Fázis 1 vizsgálóhelyre. Feladatai közé tartozik a klinikai vizsgálatok orvosi felügyelete, protokollok tervezése, betegbiztonság biztosítása, GCP és etikai előírások betartása, valamint együttműködés a vizsgálati csapatokkal innovatív terápiák fejlesztéséhez.”
“Senior Clinical Trial Associate role at ICON Plc supporting clinical trial management with administrative tasks, regulatory compliance, and cross-functional collaboration. Requires a relevant degree, experience in clinical trials, and willingness to travel (~10%). Competitive salary and benefits included.”
“ICON seeks an Assistant Manager - Financial Business Partnering in Dublin for hybrid role. Supervise finance team, oversee budgeting/forecasting for clinical trials, ensure compliance, and drive strategic financial decisions. Requires qualified accountant (ACA/ACCA/CIMA) with leadership experience in pharma/clinical research. Competitive salary and benefits included.”
“Global Regulatory Scientist position at ICON for preparing and coordinating clinical trial regulatory strategies and submissions. Requires 0-3 years of regulatory experience, ICH-GCP knowledge, and travel (~10%). Offers competitive salary, benefits, and career development in a values-driven healthcare organization.”
Icon plc | Sao Paulo
| Medicina, Inglese
“Lead Medical Writer position in Latin America for ICON, a global healthcare research organization. Responsibilities include leading medical writing for clinical documents, collaborating with cross-functional teams, mentoring junior writers, and ensuring regulatory compliance. Requires a relevant degree, strong writing skills, and experience with clinical trial data interpretation.”
Icon plc | Da casa
| Risorse Umane, Inglese
“ICON seeks a Workday HRIS Manager for hybrid/remote UK role. Lead HR tech initiatives, manage Workday systems, integrations, and team. Focus on data integrity, compliance (SOX), change management, and vendor relations. Requires 5+ years in Workday, HR processes expertise, and strong analytical skills. Competitive salary and benefits included.”
Icon plc | Sao Paulo
| Medicina, Inglese
“Clinical Research Associate (CRA) role at ICON for monitoring clinical trials, ensuring compliance with ICH-GCP, patient safety, and study documentation. Requires medical/science degree, travel (~60%), and strong communication skills. Competitive salary, benefits, and career development included.”
Icon plc | Sao Paulo
| Medicina, Inglese
“Clinical Research Associate II position in São Paulo for ICON, requiring 2+ years of experience. Responsible for site visits, data integrity, protocol compliance, and collaboration with investigators. Travel required (60% of time). Competitive salary, benefits, and career development opportunities.”
“Remote Clinical Data Coordinator (CDC II) role at ICON in Argentina. Requires a Bachelor's in Life Sciences/Healthcare, intermediate clinical data management experience, and proficiency in data systems (e.g., Medidata, Oracle RDC). Responsibilities include eCRF maintenance, data reconciliation, and regulatory compliance (ICH-GCP). Competitive salary, benefits, and career development opportunities.”
“Regulatory Operations Associate position at ICON, a global healthcare research organization. Requires 2+ years in regulatory operations within pharma/biotech, a scientific degree, and regulatory submission software proficiency. Remote role based in CDMX with competitive salary, benefits, and career development opportunities.”
“Clinical Trial Associate position at ICON, a global clinical research organization. Requires a scientific/healthcare degree, clinical research experience, and regulatory knowledge. Responsibilities include trial coordination, documentation management, and cross-functional team collaboration. Competitive salary, benefits, and career development opportunities.”
“Regular job offer for an Investigator Payments Coordinator role at ICON, a global healthcare research organization. Remote position based in Mexico. Responsibilities include managing payments to clinical trial investigators, ensuring accuracy, and collaborating with finance and clinical teams. Requires a bachelor's degree in finance/accounting and 2+ years of relevant experience.”
“Remote Pharmacovigilance Specialist role in CDMX for ICON, a global healthcare research organization. Responsible for preparing safety reports (PSURs, ICSRs), analyzing drug safety data, ensuring regulatory compliance, and collaborating with cross-functional teams. Requires scientific degree and pharmacovigilance experience.”
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