“Biedt een cruciale rol als Principal Research Pharmacist en Qualified Person (QP) bij ICON, gericht op toezicht op klinische en regelgevende aspecten van onderzoeksgeneesmiddelen. Verantwoordelijk voor protocollen, GMP/GCP-naleving, IMP-vrijgave en farmacologische expertise in fase I/IIa studies. Vereist BIG-registratie, QP-certificering en ruime ervaring in klinisch onderzoek.”
“Remote Clinical Research Associate (CRA II) position at ICON for designing and analyzing clinical trials. Requires 2+ years experience, ICH-GCP knowledge, and 60% travel. Offers competitive salary, benefits, and career development in healthcare research.”
“Clinical Trial Manager position at ICON, a global healthcare research organization. Responsible for managing clinical trial operations, ensuring compliance with regulations, and collaborating with cross-functional teams. Requires a degree in medicine/science, clinical trial experience, and willingness to travel (25%). Offers competitive salary, benefits, and career development.”
“Manager, Site Activation role at ICON in Warsaw, Poland (home or office based). Oversees clinical trial site activation, ensures regulatory compliance, and leads a team of Site Activation Leads. Requires life sciences or project management degree, strong leadership, and GCP knowledge. Competitive salary and benefits included.”
“Regular job offer for Site Services Specialist I at ICON, a global healthcare research organization. Role involves supporting clinical trial sites with logistics, issue resolution, and compliance. Requires 1+ year in call center/customer service, strong communication skills, and availability for hybrid schedule (Tue-Sat, 10AM-6PM).”
“Contrato para Analista de Contratos I em home office no Brasil, com foco em gestão de contratos, faturamento e relacionamento com clientes em pesquisa clínica. Requer experiência em contratação de sites clínicos, orçamentação e habilidades analíticas avançadas. Salário competitivo e benefícios inclusos.”
“ICON seeks a Clinical Trial Associate to support clinical trial design, data analysis, and documentation compliance. Requires a scientific/healthcare degree, clinical research experience, and strong organizational skills. Role involves cross-functional teamwork, regulatory adherence, and occasional travel (10%). Competitive salary and benefits included.”
“ICON seeks a Clinical Trial Manager to oversee trial operations, ensuring compliance with regulations and timelines. Requires a degree in medicine/science, trial management experience, and 25% travel. Offers competitive salary, health benefits, and career development in a collaborative healthcare research environment.”
“Clinical Trial Associate position at ICON, a global healthcare research organization. Requires a scientific/healthcare degree, clinical research experience, and regulatory knowledge. Involves trial coordination, documentation, and cross-functional teamwork. Competitive benefits package with salary, health coverage, and career development. Occasional travel (10%) required.”
“Oferta de emprego em São Paulo para Study Start Up Associate na ICON, empresa de pesquisa clínica. Função híbrida (3 dias escritório/2 dias remoto) com foco em iniciação de ensaios clínicos, submissão regulatória e coordenação com stakeholders. Requer experiência em pesquisa clínica, inglês avançado e habilidades organizacionais. Benefícios competitivos e pacote de recompensas.”
“ICON seeks a Study Start Up Manager (UK, remote) to lead end-to-end clinical study start-up activities, ensuring compliance, timelines, and quality. Requires CRO/pharma experience, project management, and stakeholder collaboration. Competitive salary, benefits, and inclusive workplace offered.”
“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.”
“ICON busca CRAs II para atuar no Brasil, com viagens frequentes (70% do tempo). Requisitos: experiência prévia como monitor de pesquisa clínica, conhecimento em ICH-GCP e inglês avançado. Salário competitivo e benefícios incluídos. Funções: qualificação de sites, monitoramento, revisão de dados e garantia de conformidade.”
“Clinical Research Associate (CRA II) role at ICON for designing and analyzing clinical trials, ensuring protocol compliance, data integrity, and patient safety. Requires 2+ years experience, ICH-GCP knowledge, and 60% travel. Competitive salary and benefits offered.”
“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.”
“Senior Clinical Supply Specialist role at ICON for designing and managing clinical trial labels. Requires expertise in clinical supplies, regulatory compliance (cGMP), and stakeholder collaboration. Bachelor's degree in supply chain or life sciences needed. Competitive benefits and remote work available.”
“Clinical Trial Manager role at ICON to oversee clinical trial operations, ensuring compliance, timelines, and quality. Requires 1+ year experience in CTM, monitoring expertise, and therapeutic area knowledge (immunology/psychiatry/neurology). Competitive salary, benefits, and travel (~25%) included.”
“Puesto de Asociado en Farmacovigilancia en ICON para monitorear y garantizar la seguridad de productos farmacéuticos. Requiere experiencia en farmacovigilancia, análisis de eventos adversos y cumplimiento normativo. Trabajo remoto desde CDMX con viajes ocasionales (10%). Beneficios competitivos y desarrollo profesional.”
“AI Portfolio Analyst role at ICON, a global healthcare intelligence firm, focusing on managing AI initiatives, gathering business requirements, and aligning AI capabilities with strategic priorities. Requires strong analytical skills, experience in business analysis, and familiarity with AI/ML concepts. Hybrid work model with competitive benefits.”
“Regular job offer for Site Specialist II at ICON, a global healthcare CRO. Responsible for site management, document coordination, compliance, and clinical trial operations. Requires life sciences/healthcare degree or equivalent experience, GCP knowledge, and strong organizational skills. Competitive salary and benefits included.”
“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.”
“ICON busca un Set Up Specialist I para gestionar el montaje de laboratorios en ensayos clínicos, coordinando con clientes y equipos internos. Requiere experiencia en investigación clínica, protocolos de estudio y configuración de bases de datos. Ofrece salario competitivo, beneficios integrales y desarrollo profesional en un entorno inclusivo.”
“Oferta de empleo para IT Support Engineer III en ICON México (Ciudad de México). Rol híbrido con soporte técnico a usuarios internos, gestión de incidencias en CRM (ServiceNow), resolución de problemas y mantenimiento de sistemas. Requiere experiencia en ITIL, conocimientos en redes, servidores y MS Office. Paquete de beneficios competitivo.”
“Hybrid Clinical Trial Associate (Regulatory) role in Mexico City for ICON, a global clinical research organization. Responsibilities include coordinating clinical trials, ensuring regulatory compliance (COFEPRIS, ICH-GCP), managing documentation, and supporting study start-up. Requires a Bachelor's in a scientific/healthcare field and clinical research experience.”
“Regular job offer for a Study Start Up Associate I role at ICON, a global healthcare research organization. Responsibilities include clinical trial initiation, regulatory document preparation, and stakeholder coordination. Requires a bachelor's degree in life sciences, strong organizational skills, and occasional travel (5%). Competitive salary and benefits package offered.”
“Clinical Site Associate role in Mexico for ICON, a healthcare research organization. Hybrid office-based position requiring a scientific/healthcare degree, clinical research experience, and English proficiency. Involves trial coordination, documentation, and compliance with travel requirements (10%). Offers competitive salary and benefits.”
“Clinical Trial Assistant role at ICON for designing and analyzing clinical trials, ensuring compliance with protocols and regulatory requirements. Requires a Bachelor's in a scientific/healthcare field, clinical research experience, and up to 10% travel. Competitive salary, benefits, and career development opportunities included.”
“Contract Analyst I role at ICON for healthcare intelligence and clinical research. Requires 2+ years in clinical research site contracting, budgeting, and negotiation with sites. Involves managing clinical trial agreements, budgets, and payment terms. Competitive salary, benefits, and travel (5%) included.”
“Clinical Research Associate position in Amsterdam for ICON, requiring a Bachelor's in a scientific/healthcare field and 2+ years of experience. Responsibilities include trial monitoring, data integrity, and patient safety. Role is hybrid (40% remote), with 60% travel required. Fluency in Dutch and English is mandatory.”
“ICON seeks a Pharmacovigilance Project Manager to lead drug safety projects, ensuring regulatory compliance and cross-functional team coordination. Requires extensive pharmacovigilance experience, project management skills, and a scientific degree. Competitive salary, benefits, and career development offered.”
“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 knowledge (ICH-GCP), and project management. Involves site activation, document review, and cross-functional collaboration. Travel required (~5%). Competitive benefits package included.”
“Regular job offer for Study Start-up Associate II at ICON, a global CRO. Requires 2+ years in clinical research site start-up, regulatory compliance (ICH-GCP), and strong project management. Competitive salary, benefits, and travel (5%). Remote position (LI-Remote).”
“Site Specialist II role at ICON in Warsaw, Poland, for managing site support activities, ensuring compliance, and coordinating clinical trial documentation. Requires life sciences/healthcare degree or equivalent experience, strong organizational skills, and proficiency in GCP. Competitive salary, benefits, and career development opportunities included.”
“Clinical Trial Assistant role at ICON, a global healthcare research organization. Requires a scientific/healthcare degree, clinical research experience, and regulatory knowledge. Involves trial coordination, documentation management, and cross-functional teamwork with occasional travel (10%). Competitive salary and benefits package offered.”
“ICON seeks a Clinical Logistic Distribution Specialist to manage clinical trial supply logistics, ensuring compliance with GMP/GDP standards. Requires 5+ years in regulated distribution, strong problem-solving, and cross-functional collaboration. Role includes inventory management, vendor audits, and process improvement in a remote setting.”
“ICON recrute un Global Project Manager pour piloter des projets internationaux en gestion de la recherche clinique. Missions : planification, coordination d'équipes, gestion des risques et reporting. Profil : expérience en gestion de projet, leadership, certifications PMP/PRINCE2 un plus. Salaire compétitif, avantages sociaux et voyages professionnels (30%).”
“Clinical Research Associate II role at ICON for designing and analyzing clinical trials, ensuring protocol compliance, and maintaining data integrity. Requires 2+ years of experience, ICH-GCP knowledge, and 60% travel. Competitive salary, benefits, and career development opportunities included.”
“Regular job offer for a Study Start Up Associate I at ICON, a global healthcare research organization. Role involves facilitating clinical trial initiation, ensuring regulatory compliance (including EU CTR submissions), and collaborating with stakeholders. Requires a life sciences degree and relevant experience. Competitive benefits and inclusive workplace culture.”
“Hybrid Project Assistant role (3 days office, 2 days remote) in Mexico City for ICON, supporting imaging project teams with administrative tasks, documentation, and cross-departmental coordination. Requires bachelor's degree (preferred in business/life sciences) and strong organizational skills. Competitive benefits package offered.”
“ICON seeks a remote Grants Specialist (Payment Analyst) to manage grant applications, ensure compliance, and track outcomes. Requires a Bachelor's degree, grant management experience, and proficiency in TMF/CTMS. Competitive salary, benefits, and career development offered.”
“ICON busca un Supervisor de Farmacovigilancia para supervisar el monitoreo y reporte de eventos adversos en ensayos clínicos y productos comercializados. Requiere título en ciencias de la vida o farmacia, inglés avanzado y liderazgo en equipo. Posición presencial en Buenos Aires con 1 visita mensual a oficina.”
“Regular job offer for Site Management Associate I at ICON, a global healthcare research organization. Hybrid role (3 days office, 2 days remote) based in São Paulo. Requires Bachelor's in life sciences/clinical research, 6+ months experience, advanced English, and strong organizational skills. Focus on clinical trial site monitoring, GCP compliance, and cross-functional collaboration.”
“Remote-based Safety Scientist role in UK, Poland, Bulgaria, Ireland, or Spain. Requires 2+ years in pharmacovigilance, clinical trial safety analysis, and regulatory compliance. Competitive salary, benefits, and career development in a healthcare research organization.”
“ICON busca un Clinical Contracts Associate para gestionar contratos clínicos y acuerdos de confidencialidad (NDA) en ensayos globales, negociar presupuestos y términos de pago, y asegurar facturación oportuna. Requiere título universitario en Ciencias de la Vida o Negocios, 4+ años de experiencia en biotecnología/CRO, y habilidades en Excel y bases de datos. Posición remota con beneficios competitivos.”
“Manager position at ICON for overseeing clinical data science workstreams, analyzing clinical trial data, ensuring data integrity, and mentoring teams. Requires life sciences/computer science background, regulatory knowledge, and leadership skills. Competitive salary, benefits, and travel requirements (~10%).”
“ICON seeks a Business Operations Specialist to support governance operations, reporting, and strategic initiatives in healthcare/pharmaceutical industries. Role involves managing reports, coordinating reviews, analyzing data, and optimizing processes. Requires a bachelor's degree, strong organizational skills, and cross-functional collaboration. Competitive salary and benefits included.”
“ICON seeks a Manager, Clinical Operations for home-based role with occasional office meetings. Oversees clinical trial execution, ensures regulatory compliance, and leads cross-functional teams. Requires advanced degree in life sciences, extensive clinical operations experience, and strong leadership skills. Competitive salary, benefits, and career development included.”
“ICON plc seeks a Regulatory Project Manager to lead cross-functional teams in planning, preparing, and delivering compliant regulatory submissions for pharmaceutical and biotech clients. Requires project management skills, Microsoft Project experience, and fluency in English. Offers competitive salary, benefits, and career development in a global healthcare research organization.”
es 
Italiano