“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 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.”
“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 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 experięncia em pesquisa clínica, conhecimento em GCP e habilidades de comunicaçăo e gestăo 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+ ańos 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.”
“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+ ańos 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 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 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.”
“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.”
“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.”
“Seeking a Clinical Research Associate II (CRA II) in Săo 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.”
“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.”
“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.”
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“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.”
“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.”
“Clinical Research Associate II position in Săo 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.”
“Proyecto de gestión de ensayos clínicos en laboratorio para ICON, empresa de investigación clínica. Requiere experiencia en gestión de proyectos, comunicación y manejo de estudios clínicos. Ofrece salario competitivo, beneficios integrales y oportunidades de desarrollo profesional. Posición remota en México.”
“Principal Study Start-Up Associate position at ICON in Romania for leading clinical trial start-up activities, including CTA negotiations, regulatory submissions, and budget oversight. Hybrid role requiring 1-3 days in office. Requires strong regulatory and contract negotiation experience in clinical research.”
“Clinical Research Associate (CRA II) position in Săo Paulo for ICON, a global clinical research organization. Requires 2+ years of experience, Bachelor's in scientific/healthcare field, and knowledge of ICH-GCP guidelines. Role involves monitoring clinical trials, ensuring compliance, data integrity, and patient safety. Competitive salary, benefits, and travel required (~60%).”
“ICON busca un Digital Health Enablement Manager para liderar proyectos de implementación y gestión de tecnologías digitales en ensayos clínicos (eCOA, Imaging, ECG, etc.). Requiere experiencia en ensayos clínicos, gestión de proyectos y conocimientos en plataformas digitales. Trabajo 100% remoto desde México con beneficios competitivos.”
“ICON busca un Set Up Specialist para gestionar el montaje de laboratorios en ensayos clínicos, coordinando con clientes, protocolos y equipos internos. Requiere experiencia en investigación clínica, gestión de bases de datos y cumplimiento normativo (GCP). Ofrece salario competitivo, beneficios integrales y desarrollo profesional.”
“Seeking a Talent Sourcing Recruiter for ICON, a global healthcare intelligence and clinical research organization. Responsibilities include building talent pipelines, sourcing qualified candidates in life sciences/healthcare, and engaging with candidates via job boards, social media, and networking. Requires HR or related degree, recruiting experience, and strong communication skills.”
“Se busca un Drug Safety Associate en CDMX para ICON, organización global en investigación clínica. Requisitos: licenciatura en ciencias de la salud, 1-2 ańos de experiencia en farmacovigilancia, conocimiento de regulaciones ICH/FDA/EMA. Responsabilidades: revisión de eventos adversos, codificación, reportes regulatorios y colaboración en equipos multidisciplinarios.”
“ICON busca Project Manager en México para liderar proyectos en Medical Affairs. Responsable de planificación, coordinación de equipos multidisciplinarios y entrega de proyectos dentro de presupuesto y plazos. Requiere experiencia en gestión de proyectos, liderazgo y herramientas como PMP/PRINCE2. Viajes ocasionales (30%). Beneficios competitivos y enfoque en inclusión.”
“Lead clinical data programming for global trials from home in Mexico, Colombia, Brazil, Chile, or Peru. Oversee SAS/Python/SQL-based analysis, ensure CDISC/FDA/EMA compliance, and mentor teams. Requires pharma/CRO experience, leadership, and 15% travel. Competitive salary and benefits included.”
“Clinical Research Associate I position in Săo Paulo or Rio de Janeiro for ICON, a global clinical research organization. Requires university degree in medicine/science, ICH-GCP knowledge, and 60% travel. Responsibilities include study monitoring, documentation, and stakeholder collaboration. Competitive salary and benefits offered.”
“Contract Analyst II position at ICON for home-based work in Spain. Requires 2+ years in contract management, preferably in pharmaceuticals/clinical research. Duties include reviewing contracts, negotiating terms, assessing risks, and ensuring regulatory compliance. Competitive salary and benefits package offered.”
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