Lavori presso Icon plc

“Senior Clinical Research Associate (CRA II) role at ICON for designing and monitoring clinical trials. Requires 2+ years experience, ICH-GCP knowledge, and 60% travel. Offers competitive salary, benefits, and career development in a collaborative healthcare research environment.”

“Senior Contract Analyst position at ICON, a global healthcare research organization. Responsible for managing contractual agreements, ensuring compliance, and mentoring colleagues in contract negotiation and risk analysis. Requires a Bachelor's degree, contract management experience in pharmaceutical/clinical research, and occasional travel (5%). Offers competitive salary, benefits, and career development.”

“Clinical Sample Processor I role at ICON for processing and tracking clinical trial samples. Requires a scientific degree, lab experience, and attention to detail. Offers competitive salary, benefits, and career development in a healthcare research organization.”

“ICON seeks a Site Specialist II in Madrid or Barcelona for clinical trial site support. Role involves managing site documentation, coordinating logistics, and improving workflows. Requires fluency in English/Spanish, life sciences/healthcare background, and GCP knowledge. Competitive salary, benefits, and career development offered.”

“Financial Analyst II role at ICON in Dublin, offering hybrid work. Ideal for newly qualified ACA/ACCA/CIMA accountants or those transitioning from Big 4/Top 10 firms. Involves financial analysis, forecasting, business partnering, and commercial exposure with structured career progression.”

“Oferta de empleo híbrido en Ciudad de México para Associate I en Start-Up de Estudios Clínicos en ICON. Requiere título universitario en ciencias de la vida, experiencia en investigación clínica o asuntos regulatorios, dominio avanzado de inglés y habilidades organizacionales. Responsabilidades incluyen preparación de documentos regulatorios, coordinación con stakeholders y apoyo en ensayos clínicos.”

“Full-time Clinical Study Coordinator rol in Groningen bij ICON, verantwoordelijk voor coördinatie, uitvoering en naleving van klinische studies. Vereist relevante ervaring, Bachelor in wetenschap, GCP-kennis en sterke organisatorische/communicatieve vaardigheden. Nederlands en Engels vereist.”

“Principal Medical Writer role at ICON for leading regulatory and clinical document development, including study reports, protocols, and approval applications. Requires life sciences/pharmacy degree, regulatory expertise, and team leadership. Competitive salary, benefits, and career growth opportunities.”

“Contract Analyst II role at ICON for clinical trial contract management. Requires 2+ years in contract administration, preferably in pharma/clinical research. Responsibilities include reviewing contracts, negotiating terms, risk assessment, and ensuring regulatory compliance. Competitive salary, benefits, and travel (5%) included.”

“Revenue Accountant position in Dublin (Hybrid) at ICON, a healthcare research organization. Requires ACA/ACCA/CIMA qualification, revenue accounting experience (ASC 606), and proficiency in Excel/ERP systems. Focus on financial analysis, revenue recognition for clinical trials, and audit support.”

“BIG-geregistreerde Medical Research Associate voor klinisch geneesmiddelenonderzoek bij ICON. Taken: verpleegtechnische handelingen, dataregistratie, deelnemersbegeleiding en protocoluitvoering. Vereist MBO niveau, BIG-registratie en zorgervaring. Flexibele inzetbaarheid, inclusief avond/nacht/weekenddiensten.”

“IT Resource Manager role at ICON in Dublin 18, Leopardstown. Manages IT contractor sourcing, onboarding, and engagement for IT GBS. Requires IT/vendor experience, leadership, and process improvement focus. Hybrid office role with 5% travel. Competitive salary and benefits offered.”

“Regular job offer for a Clinical Research Associate (CRA) role at ICON, requiring 12+ months of monitoring experience, preferably in Oncology trials. Based in the UK, with 60% travel. Competitive salary, benefits, and career development opportunities in clinical trial monitoring.”

“ICON busca un Project Manager especializado en Imaging para gestionar proyectos clínicos relacionados con imágenes médicas. Requiere experiencia en gestión de proyectos en ensayos clínicos o industria farmacéutica, liderazgo y comunicación. Ofrece salario competitivo, beneficios de salud y desarrollo profesional en un entorno inclusivo.”

“Puesto híbrido en Ciudad de México para Manager de Operaciones Clínicas en ICON, empresa global de investigación clínica. Liderarás la planificación y ejecución de ensayos clínicos, gestionarás equipos y garantizarás cumplimiento normativo. Requiere experiencia en operaciones clínicas, liderazgo y disposición para viajar (30%). Beneficios competitivos y desarrollo profesional.”

“Clinical Scientist role in Colombia for ICON, designing and conducting clinical studies. Requires a relevant Bachelor's degree, clinical research experience, and strong analytical skills. Involves protocol design, data analysis, cross-functional collaboration, and regulatory submissions. Competitive salary, benefits, and travel requirements (~20%).”

“ICON seeks a Clinical Research Associate (CRA II) to design, monitor, and analyze clinical trials, ensuring protocol compliance, data integrity, and patient safety. Requires 2+ years of experience, ICH-GCP knowledge, fluency in German and English, and 60% travel. Competitive salary and benefits included.”

“Clinical Site Associate role at ICON, a global healthcare research organization. Hybrid office-based position requiring a scientific/healthcare degree, clinical research experience, and regulatory knowledge. Involves trial coordination, documentation management, and cross-functional collaboration. Competitive benefits package included.”

“Puesto de CRA II en CDMX para ICON, empresa global en investigación clínica. Requiere título universitario en ciencias/medicina, 2+ años como CRA, conocimiento de ICH-GCP y 60% de viajes. Ofrece salario competitivo, beneficios de salud, desarrollo profesional y trabajo en equipo para monitoreo de ensayos clínicos.”

“ICON busca un Clinical Trial Associate para coordinar y administrar ensayos clínicos, garantizando cumplimiento normativo y apoyo en documentación. Requiere título en ciencias de la salud, experiencia en investigación clínica y habilidades organizativas. Incluye beneficios competitivos y posibilidad de viajar (10%).”

“Clinical Site Associate role in Sweden with hybrid work arrangement. Requires a Bachelor's in life sciences, 12+ months of CTA/Clinical Trial Assistant experience, ICH GCP knowledge, and strong communication skills. Responsibilities include site management, data accuracy, investigator coordination, and travel as needed. Competitive salary and benefits package offered.”

“ICON Plc busca Clinical Trial Manager para liderar la planificación, ejecución y cierre de ensayos clínicos, garantizando cumplimiento de plazos, presupuestos y regulaciones. Requiere título universitario en medicina o ciencia, experiencia en monitoreo clínico y capacidad de viajar hasta un 20%. Ofrece paquete de beneficios competitivo y desarrollo profesional.”

“Regular job offer for a PV Assistant role at ICON, a healthcare research organisation. Based near Gatwick (1-2 days office presence). Responsibilities include product returns handling, credit requests, and database entry. Requires scientific/healthcare degree and PV experience. Competitive salary and benefits package offered.”

“ICON seeks a Clinical Research Associate (CRA) with 2+ years of experience to monitor clinical trials, ensure protocol compliance, and maintain data integrity. Role involves site visits (60% travel), collaboration with investigators, and adherence to ICH-GCP guidelines. Requires a scientific degree, Italian certification, and strong organizational skills.”

“ICON busca un asistente en farmacovigilancia para trabajo remoto en CDMX. Requiere título en ciencias de la vida, farmacia o afín, experiencia en farmacovigilancia y atención al detalle. Responsabilidades incluyen gestión de reportes de eventos adversos, cumplimiento normativo y documentación precisa en bases de datos.”

“Regular job offer for Study Start Up Associate II at ICON, a global healthcare research organization. Requires 2+ years in clinical research or regulatory affairs, strong regulatory knowledge (ICH-GCP), and US experience. Role involves leading clinical trial initiation, managing regulatory submissions, and coordinating with sites. Full remote position supporting North America (US/CAN).”

“Clinical Research Associate II position based in Madrid, requiring 2+ years of experience in clinical trial monitoring. Responsibilities include site visits, data integrity, protocol compliance, and collaboration with investigators. Travel required (~60%). Competitive salary and benefits package offered.”

“Patient Recruitment Lead role at ICON, a global healthcare and clinical research organization. Responsible for developing and executing patient recruitment strategies for clinical trials, collaborating with cross-functional teams, analyzing recruitment data, and ensuring compliance with regulatory standards. Requires a Bachelor's degree in life sciences/healthcare and proven experience in patient recruitment.”

“Voor het laboratorium in Groningen zoekt ICON een Sample Processing Specialist (HBO/WO medische richting). De rol omvat coördinatie van sampleverwerking, verzending en labmanuals, met focus op deadlines en multidisciplinaire samenwerking. Vereist uitstekende communicatie en beheersing van Nederlands en Engels.”

“ICON seeks a Regulatory Scientist to develop regulatory strategies for clinical programs, prepare submissions, and ensure compliance with global requirements. Requires advanced degree in life sciences/pharmacy, regulatory affairs experience, and strong scientific/analytical skills. Full-time role with competitive benefits.”

“CRC Associate role in Northamptonshire for ICON, a healthcare research organization. Supports clinical trial coordination, data quality, and patient safety under GCP guidelines. Requires life sciences/nursing/pharmacy degree or equivalent. Office-based position with competitive benefits.”

“Site Specialist II role at ICON, a global healthcare CRO, requiring Greek and English fluency. Manages site operations, contracts, and compliance for clinical trials. Offers competitive salary, benefits, and career development in a collaborative, values-driven environment.”

“Site Specialist II role at ICON in Madrid, Spain, for managing site support activities, ensuring clinical trial compliance, and coordinating site operations. Requires French/English fluency, life sciences/healthcare background, and GCP knowledge. Offers competitive salary, benefits, and career development in a values-driven healthcare CRO.”

“ICON seeks a Site Selection Lead for Sofia, Bulgaria, to strategically identify and recommend investigator sites for clinical trials. Role involves data analysis, cross-functional coordination, and performance monitoring. Requires life sciences/healthcare background and clinical research experience. Competitive benefits package offered.”

“Site Specialist II role at ICON for global healthcare research, managing site support, clinical trial operations, and documentation compliance. Requires life sciences/healthcare degree or equivalent experience, strong organizational skills, and GCP knowledge. Offers competitive benefits and career development in a collaborative, values-driven environment.”

“Oferta de empleo como TMF Lead en ICON, organización global de investigación clínica. Rol híbrido en CDMX, enfocado en gestión de Trial Master Files, cumplimiento regulatorio y colaboración con equipos multidisciplinarios. Requiere experiencia en TMF, habilidades organizacionales y compromiso con inclusión.”

“Regular job offer for a Resource Planning Specialist in Warsaw, Poland (60% office-based). Requires experience in resource planning, workforce management, and project management within clinical research or pharmaceutical industry. Competitive salary, benefits, and career development opportunities.”

“Oferta de empleo como Patient Recruitment Associate II en ICON, organización global en investigación clínica. Responsable de planificar, coordinar y optimizar reclutamiento y retención de pacientes en ensayos clínicos, colaborando con equipos y sitios. Requiere experiencia en reclutamiento, habilidades analíticas y comunicación efectiva. Paquete de beneficios competitivo y enfoque en desarrollo profesional.”

“ICON plc busca un Clinical Research Associate II o Senior CRA para gestionar ensayos clínicos en Países Bajos. Requiere experiencia en monitoreo de ensayos Fase II-IV, conocimiento de ICH-GCP y dominio de holandés e inglés. Puesto 100% remoto con viajes ocasionales por el país.”

“Offre d'emploi pour un Clinical Research Associate II (CRA II) en pharmacie, basé à Paris ou Lyon. Poste hybride ou 100% télétravail. Missions : monitoring de essais cliniques (Phases II-IV), gestion de sites, conformité ICH-GCP, collaboration avec investigateurs. Profil : Bac+3 scientifique, 2 ans d'expérience en CRA, maîtrise français/anglais.”

“ICON seeks a CRA II for clinical trial monitoring in FSP model, requiring 2+ years experience, ICH-GCP knowledge, and 60% travel. Role involves study setup, monitoring, stakeholder collaboration, and patient safety compliance. Competitive salary and benefits included.”

“ICON busca un Clinical SDTM Programmer (avanzado) para liderar la supervisión y desarrollo de paquetes SDTM en ensayos clínicos, asegurando cumplimiento con estándares CDISC y requisitos regulatorios (FDA, PMDA). Requiere experiencia en SAS, SDTM, define.xml y colaboración con equipos globales. Oferta con estabilidad a largo plazo y enfoque en gobernanza técnica.”

“Central Monitor position in Mexico for ICON, a global healthcare research organization. Responsible for remote review and analysis of clinical trial data to ensure quality and patient safety. Requires a degree in life sciences or related field, clinical trial experience, and strong analytical skills. Offers competitive salary, benefits, and career development opportunities.”

“Project Manager, Feasibility Site Activation role in Poland for ICON, a global healthcare research organisation. Responsible for planning and managing feasibility and site activation activities for clinical studies, including timelines, regulatory submissions, and cross-functional coordination. Requires experience in clinical research, strong project management skills, and willingness to travel (10%). Competitive salary and comprehensive benefits package offered.”

“Seeking a Clinical Research Associate (CRA I or II) in São Paulo to monitor clinical trials, ensure compliance with ICH-GCP guidelines, and maintain study documentation. Requires a science/medicine degree, English proficiency, and 60% travel. Competitive salary, benefits, and career development offered.”

“Graduate Pharmacovigilance Associate role at ICON for recent graduates to support drug safety monitoring, adverse event data processing, and regulatory reporting. Requires a Bachelor's in pharmacy/life sciences, attention to detail, and English proficiency. Offers competitive salary, benefits, and career development in a global healthcare organization.”

“Clinical Research Associate II (CRA II) position at ICON Biotech in Paris or Lyon. Hybrid role requiring residency in France. Monitors Phase II-IV clinical trials, ensures ICH-GCP compliance, manages oncology/biotech studies, and handles site visits. Requires life sciences degree, CRA experience, and fluency in French/English.”

“ICON busca un Study Start Up Associate II para liderar la preparación y presentación de documentos regulatorios en ensayos clínicos en Guatemala. Requiere título en ciencias de la vida y 2+ años de experiencia en investigación clínica o asuntos regulatorios. Ofrece salario competitivo, beneficios integrales y oportunidades de desarrollo profesional.”

“ICON plc busca Clinical Research Associate II (CRA II) para rol remoto en Países Bajos. Gestionar ensayos clínicos (Fase I-III) en Biotech, garantizando cumplimiento ICH-GCP y normativas. Requiere experiencia mínima 2 años, dominio neerlandés e inglés, licencia de conducir y viajes nacionales. Ofrece desarrollo profesional y paquete de beneficios competitivo.”

“IPG Systems Analyst position in Dublin, Ireland, for a global healthcare CRO. Hybrid role requiring Bachelor's degree, experience with site budgets/payments, and system setup. Involves cross-department collaboration, system troubleshooting, and commercial focus. Competitive salary and benefits included.”