Graduate Jobs at Icon plc

“CIAM Specialist/Engineer role at ICON for designing and implementing secure identity solutions (SSO, OAuth2, OIDC, SAML) using Microsoft Entra ID/B2C. Requires experience in B2B/B2C identity solutions, compliance, and cloud environments. Offers competitive salary, benefits, and hybrid work options.”

“ICON busca un CRA II para diseñar y analizar ensayos clínicos, asegurando cumplimiento de protocolos, integridad de datos y seguridad del paciente. Requiere título en ciencias/medicina y 2+ años de experiencia en monitoreo clínico. Viajes frecuentes (60%). Paquete de beneficios competitivo.”

“Clinical Research Associate I position at ICON in Buenos Aires. Requires a university degree in medicine/science, 6 months of on-site CRA experience, ICH-GCP knowledge, and 60% travel. Offers competitive salary, health benefits, and career development in clinical trial monitoring.”

“Clinical Research Associate II role at ICON for designing and monitoring clinical trials. Requires 1+ year of experience, scientific degree, ICH-GCP knowledge, and 60% travel. Based in Buenos Aires with competitive salary, benefits, and career development.”

“ICON seeks a Clinical Data Science Lead in Mexico for remote work. Role involves leading data science initiatives in clinical trials, designing analytical strategies, mentoring teams, and communicating insights to stakeholders. Requires clinical data science experience, statistical expertise, and leadership skills. Competitive salary and benefits included.”

“Site Contract Manager role at ICON for contract management in clinical trials, requiring 2+ years of experience in contract administration, strong analytical skills, and regulatory knowledge. Responsibilities include reviewing contracts, negotiating terms, and collaborating with cross-functional teams. Competitive benefits and inclusive workplace offered.”

“Clinical Data Coordinator role at ICON in Warsaw, Poland. Hybrid position (3 days on-site). Requires Master's in Life Sciences/Healthcare, fluency in English, and experience in clinical data management. Involves designing CRFs, reviewing clinical data, issuing queries, and ensuring study timelines. Competitive salary and benefits included.”

“Clinical Research Associate role at ICON in Milan requiring 2+ years of experience, ICH-GCP knowledge, and 60% travel. Responsibilities include trial monitoring, site visits, data integrity, and protocol compliance. Competitive salary, benefits, and career development offered.”

“Clinical Trial Manager role at ICON, a global clinical research organization. Responsible for managing day-to-day clinical trial operations, ensuring timelines, budget, and quality standards. Requires experience in clinical trial management, therapeutic expertise, and willingness to travel (25%). Offers competitive salary, benefits, and career development opportunities.”

“Hybrid Clinical Data Coordinator I position in Poland for ICON, requiring a Master's in Life Sciences/Healthcare, clinical data management experience, and knowledge of regulatory guidelines (ICH-GCP). Responsibilities include eCRF development, data review, query issuance, and cross-functional collaboration. Competitive salary, benefits, and career development opportunities included.”

“Clinical Trial Associate position at ICON, a global healthcare CRO. Requires a scientific/healthcare degree, clinical research experience, and regulatory knowledge. Involves trial coordination, documentation, and cross-functional collaboration. Competitive salary, benefits, and travel (10%) included.”

“Lead Consultant position at ICON for Systematic Reviews & Evidence Synthesis, remote-based role requiring a Master's/PhD in public health or related field. Responsibilities include managing SLRs/NMAs, client relations, team leadership, and business development. Competitive salary, benefits, and travel (15%) included.”

“Clinical Research Associate (CRA II) position in Chile for ICON, requiring 2+ years of experience in clinical trial monitoring. Responsibilities include site visits, data integrity, protocol compliance, and collaboration with investigators. Position involves 60% travel. Competitive salary and benefits offered.”

“Reguliere fulltime functie (40 uur/week) als facilitair medewerker in Groningen voor ICON, een wereldwijd klinisch onderzoeksbedrijf. Taken omvatten beheer van medische apparatuur, planning onderhoud, verhuizingen, klein onderhoud en coördinatie met interne/externe partijen. Vereist MBO-4 niveau, zelfstandigheid, proactiviteit en goede Engelse vaardigheden.”

“ICON seeks a Clinical Trial Liaison to design, analyze, and implement clinical trial strategies, ensuring compliance and data accuracy. Requires a relevant degree, clinical research experience, and strong stakeholder communication. Offers competitive salary, benefits, and career development in a values-driven healthcare organization.”

“Remote Clinical Research Associate II position in Poland. Requires 1+ year of experience, ICH-GCP knowledge, and site monitoring skills. Involves trial design, data analysis, and ensuring protocol compliance. Competitive salary, benefits, and career development opportunities offered.”

“Seeking a Clinical Research Associate in São Paulo to monitor clinical trials, ensure compliance with ICH-GCP guidelines, and maintain study documentation. Requires a science/medicine degree, strong communication skills, and 60% travel. Competitive salary, benefits, and career development opportunities.”

“Site Contract Negotiator role at ICON for reviewing and negotiating clinical trial agreements and budgets. Requires legal/business background, contract management experience, and strong attention to detail. Offers competitive salary, benefits, and career development in healthcare research.”

“ICON Plc busca un Clinical Trial Manager para liderar la planificación, ejecución y cierre de ensayos clínicos en enfermedades del sistema nervioso central y raras, garantizando plazos, presupuestos y cumplimiento normativo. Requiere título universitario en medicina o ciencias, experiencia en monitoreo clínico y capacidad para viajar hasta un 20%. Ofrece salario competitivo y beneficios integrales.”

“ICON busca Clinical Trial Manager para gestão operacional remota de ensaios clínicos no Brasil. Requisitos: experiência em CTM ou equivalente, gestão de estudos Fase III/IV, liderança de equipe e conhecimento em RBM. Viagens de ~15%. Salário competitivo e benefícios.”

“Regular job offer for a Cardiac Data Processing Specialist at ICON, a global healthcare research organization. Responsibilities include reviewing and processing cardiac data for clinical trials, ensuring data quality, and maintaining compliance with regulatory standards. Requires relevant experience in cardiac sciences or clinical trials, attention to detail, and proficiency in clinical data systems.”

“Clinical Research Associate (CRA) role in São Paulo for ICON, a global clinical research organization. Requires a degree in medicine/science, ICH-GCP knowledge, and 60% travel. Responsibilities include study monitoring, documentation, stakeholder coordination, and ensuring regulatory compliance. Competitive salary, benefits, and career development opportunities offered.”

“Remote Clinical Research Associate II position in Mexico for ICON. Requires 2+ years of experience, a scientific degree, and 60% travel. Responsibilities include monitoring clinical trials, ensuring compliance, and collaborating with site staff. Competitive salary and benefits offered.”

“Junior Clinical Research Associate (CRA) role at ICON for clinical trial monitoring. Requires degree in medicine/science, ICH-GCP knowledge, and 60% travel. Competitive salary, benefits, and career growth in healthcare intelligence.”

“ICON seeks a Proposals Writer II to craft compelling RFP responses in healthcare/CRO industry. Requires 2-5 years writing experience, science/communications background, and proficiency in Word. Role involves collaborating with experts, managing deadlines, and driving business growth in a fast-paced, values-driven environment.”

“ICOM seeks a Clinical Research Associate II (FSP - Sponsor Dedicated) in Buenos Aires, Argentina. Requires a Bachelor's degree in a scientific/healthcare field, 2+ years of CRA experience, advanced English, and ICH-GCP knowledge. Role involves site monitoring, data integrity, patient safety, and 60% travel. Competitive salary, benefits, and career development included.”

“Full-time Clinical Research Associate I role at ICON, requiring a science/medicine degree and 6+ months CRA experience. Involves trial monitoring, travel (~60%), compliance with ICH-GCP, and stakeholder coordination. Offers competitive salary, benefits, and career development.”

“Regular job offer for a Site Engagement Liaison at ICON, a global healthcare research organization. Role involves building relationships with clinical trial sites, ensuring compliance with protocols, and supporting study conduct. Requires a Bachelor's in life sciences, clinical research experience, and 60% travel. Competitive benefits package included.”

“Clinical Trial Manager position at ICON in Buenos Aires to oversee clinical trial operations, ensuring compliance with regulations, managing timelines/budgets, and collaborating with cross-functional teams. Requires a degree in Medicine/Life Sciences, oncology experience preferred, and advanced English. Office attendance once weekly.”

“Regular job offer for a Study Start Up Associate role at ICON in Sofia, Bulgaria. Requires fluency in English and one other European language, a Bachelor's in life sciences, and experience in clinical research or regulatory affairs. Duties include facilitating clinical trial initiation, regulatory document preparation, and stakeholder coordination. Competitive benefits package offered.”

“Remote role for a Data Risk Analyst at ICON, a global clinical research organization. Responsibilities include conducting risk assessments on clinical trial data, collaborating with cross-functional teams, and ensuring data integrity and regulatory compliance. Requires a degree in statistics/life sciences, clinical data analysis experience, and strong analytical skills.”

“Hybrid Regulatory Technician role at ICON providing operational support for regulatory submissions, maintaining documentation, and ensuring compliance. Requires life sciences/pharmacy degree or equivalent experience, attention to detail, and regulatory affairs experience. Offers competitive salary, benefits, and career development in a values-driven healthcare organization.”

“Senior finance leadership role in Dublin for ICON, a global healthcare research organization. Oversees global internal audit function, ensuring governance, risk management, and SOX compliance. Requires ACA/ACCA/CPA/CIA qualification, Big 4 experience, and hybrid work (3 days office). Competitive salary and benefits included.”

“QA Test Manager role at ICON leading AI platform testing, defining test strategies, managing QA teams, and ensuring compliance for AI-powered solutions. Requires experience in QA leadership, automation, CI/CD, and AI/ML testing in regulated environments. Hybrid/remote option available.”

“Clinical Trial Manager II role at ICON overseeing clinical trial management, designing protocols, ensuring regulatory compliance, analyzing data, and collaborating with cross-functional teams. Requires clinical trial experience, strong analytical skills, and willingness to travel (25%). Competitive salary and benefits included.”

“Senior finance leadership role in Dublin (hybrid) for ICON, a global healthcare research firm. Responsible for enterprise-wide FP&A, strategic decision support, M&A financial leadership, and SOX-compliant governance. Requires extensive experience in public company environments, strong analytical skills, and executive presence. Competitive salary and benefits included.”

“Senior AI Architect role at ICON for defining and governing AI platforms, frameworks, and services. Requires expertise in cloud-native systems, AI/ML, microservices, and distributed architectures. Hybrid position with competitive salary, benefits, and career development opportunities.”

“Fixed-term contract role at ICON supporting business development by preparing high-quality clinical trial proposals and budgets. Involves coordinating with teams, adhering to processes, and ensuring timely submissions. Requires occasional travel (5%). Competitive benefits package offered.”

“ICON busca un Site Management Associate II con dominio del neerlandés para supervisar ensayos clínicos en Bulgaria, España o Polonia. Requiere título universitario en ciencias de la vida o investigación clínica, experiencia en gestión de sitios y conocimiento de GCP. Ofrece salario competitivo, beneficios integrales y oportunidades de desarrollo profesional.”

“ICON seeks an AI Compliance Lead to develop and enforce responsible AI frameworks, ensuring compliance with regulations like EU AI Act and GDPR. Role involves governance, risk management, and embedding ethical standards across AI products in a healthcare-focused organization. Hybrid/remote position with competitive benefits.”

“Clinical Trial Manager position in Bucharest, Romania. Hybrid role managing clinical trial operations, ensuring compliance with regulations, and collaborating with cross-functional teams. Requires medical/science degree, trial management experience, and 25% travel. Competitive salary and benefits package offered.”

“ICON recrute un Project Manager IRT pour superviser la mise en œuvre de solutions Interactive Response Technology (IRT) dans des essais cliniques. Missions : gestion de projets, collaboration avec équipes pluridisciplinaires, respect des délais et normes réglementaires. Profil : expérience en gestion de projets cliniques, leadership, compétences organisationnelles. Avantages : salaire compétitif, couverture santé, développement professionnel.”

“ICOM seeks a Clinical Trial Manager to oversee trial operations, ensuring compliance with regulations, managing timelines/budgets, and collaborating with cross-functional teams. Requires a science/medicine degree, clinical trial experience, and 25% travel. Competitive salary and benefits included.”

“Regular job offer for a Clinical Research Associate (CRA I) at ICON, a global healthcare organization. Requires a university degree in medicine/science, ICH-GCP knowledge, and 60% travel. Offers competitive salary, benefits, and career development in clinical trial monitoring.”

“Oferta de empleo en Ciudad de México para Site Management Associate II en ICON, organización de investigación clínica. Requiere título universitario en ciencias de la vida o área relacionada, 2+ años de experiencia en investigación clínica, gestión de TMF y conocimiento de GCP. Rol administrativo y operativo en ensayos clínicos con salario competitivo y beneficios.”

“ICON seeks an in-house Clinical Research Associate (IHCRA) to manage clinical studies, ensure regulatory compliance, and oversee site operations. Requires experience in clinical trial coordination, GCP knowledge, and proficiency in VeeVa Systems, Ariba, Apex, RGPS, and Grant Plan. Competitive salary and benefits included.”

“Principal Medical Writer position at ICON for leading regulatory/clinical document development, mentoring junior writers, and managing approval applications for new biologics/drugs. Requires life sciences/pharmacy degree, strong regulatory writing experience, and neuroscience expertise as a plus. Competitive benefits included.”

“ICHICON seeks a qualified lawyer (4-6 years PQE) for a hybrid (60% office-based) Legal Counsel role in Dublin. Responsibilities include M&A, corporate transactions, debt financing, and internal reorganizations. Requires strong transactional experience, strategic thinking, and team collaboration. Competitive salary, benefits, and career growth opportunities provided.”

“Sponsor Assurance Lead role at ICON in Dublin (Hybrid) to ensure AI product compliance, governance, and transparency for sponsors. Requires 5+ years in assurance/compliance, regulatory knowledge (GDPR, EU AI Act), and client-facing experience. Competitive benefits included.”

“Contract Analyst I role at ICON, a global healthcare intelligence firm. Responsibilities include preparing, verifying, and executing invoicing, reconciling accounts, and maintaining client relationships. Requires a Bachelor's degree in Finance/Accounting/Business Administration, relevant experience, and strong analytical skills. Competitive salary, benefits, and career development opportunities offered.”