“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 São 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 años 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 São 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.”
“Full-time Clinical Research Associate (CRA II) role at ICON for designing and analyzing clinical trials with 2+ years experience. Responsibilities include site visits, data integrity, protocol compliance, and travel (~60%). Requires German/English fluency, ICH-GCP knowledge, and scientific degree. Competitive salary and benefits offered.”
“CRA II position in São Paulo for clinical trial monitoring at ICON, requiring 2+ years of experience. Responsibilities include site visits, data integrity, protocol compliance, and collaboration with investigators. Competitive salary, benefits, and travel required (60%).”
“CRA II position at ICON in Mexico for remote work. Requires 2+ years as a Clinical Research Associate, knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. Responsibilities include site monitoring, data review, and ensuring protocol compliance. Competitive salary and benefits package offered.”
“ICON busca un Lead Business Operations Specialist especializado en RBQM (Risk-Based Quality Management) para liderar la implementación de estrategias de supervisión de calidad en ensayos clínicos. Requiere experiencia en investigación clínica, conocimiento de ICH E6/E8 y habilidades de gestión de riesgos. Ofrece paquete de beneficios competitivo y oportunidades de desarrollo.”
“Supervisor role in Finance Business Partnering at ICON, Dublin. Requires ACA/ACCA/CIMA qualification with 3+ years experience, managing finance teams for clinical projects. Hybrid position offering competitive salary, benefits, and career development in healthcare intelligence.”
“ICON seeks a CMC Project Manager to lead regulatory affairs CMC projects in biologics drug development. Role involves project planning, milestone tracking, stakeholder management, and risk mitigation. Requires Life Sciences degree, CMC experience, and proficiency in MS Project/Planisware. Competitive salary and benefits included.”
“Contract Analyst I position in Mexico at ICON, a global healthcare research organization. Requires 2+ years in contract management, preferably in pharma/clinical trials, with strong legal/regulatory knowledge. Duties include contract review, negotiation, risk assessment, and compliance. Advanced Excel and English skills required. Remote role with competitive benefits.”
“Full-time Clinical Research Associate II role at 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 package offered.”
“Home-based Clinical Research Associate II role in Lisbon for ICON, a global clinical research organization. Requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. Offers competitive salary, benefits, and career development in clinical trial monitoring and data integrity.”
“Remote Clinical Data Coordinator (CDC II) role at ICON for designing and analyzing clinical trials, managing eCRF, data reconciliation, and ensuring high-quality clinical data management in the pharmaceutical/biotech industry. Requires a Bachelor's in Life Sciences/Healthcare, intermediate CDM experience, and knowledge of regulatory guidelines (ICH-GCP).”
“ICON seeks a Clinical Research Associate II to monitor clinical trials, ensuring compliance with ICH-GCP guidelines and regulatory requirements. Role involves coordinating study setup, maintaining documentation, and collaborating with stakeholders. Requires a science/medicine degree, travel (~60%), and strong communication skills. Competitive salary and benefits included.”
“ICON seeks a Clinical Trial Manager to oversee trial operations, ensuring compliance with regulations, timelines, and budgets. Requires a degree in medicine/science, clinical experience, and 25% travel. Competitive salary, health benefits, and career development included.”
“ICON seeks a Clinical Project Manager to lead healthcare research projects, ensuring timely delivery within budget and quality standards. Requires bachelor's degree, project management experience, leadership skills, advanced Spanish, and 30% travel. Competitive salary, benefits, and career development offered.”
“Project Manager en oncologie chez ICON, organisation spécialisée en recherche clinique et intelligence médicale. Gestion de projets en coordination avec des équipes pluridisciplinaires, suivi des budgets et délais, avec 30% de déplacements requis. Expérience en gestion de projet et leadership exigée.”
“Clinical Research Associate I role at ICON in Buenos Aires. Requires medical/science degree, ICH-GCP knowledge, and 35% travel. Responsible for clinical trial monitoring, patient safety, and stakeholder coordination. Offers competitive salary, benefits, and career development.”
“Oferta de emprego para Associate Project Manager em Serviços Linguísticos, com foco em gestão de projetos de COAs e validação linguística. Requer experiência em localização, TMS/CAT tools e pesquisa clínica. Vaga homebased no Brasil, com benefícios competitivos e foco em compliance e qualidade.”
“Financial Analyst II position in Dublin for ICON, a healthcare research organization. Hybrid role requiring 2-4 years of experience, ACA/ACCA/CIMA qualification, and expertise in financial modeling and analysis. Competitive salary, benefits, and career development opportunities.”
“Clinical Trial Manager role 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 strong problem-solving skills. Competitive salary and benefits package offered.”
“Regular job offer for a Study Start Up Associate at ICON, a global healthcare research organization. Responsibilities include facilitating clinical trial initiation, regulatory compliance, and stakeholder coordination. Requires a Bachelor's degree in life sciences, strong organizational skills, and willingness to travel (5%). Competitive salary and benefits package offered.”
“Clinical Trial Manager role in Oncology at ICON, a global CRO. Responsibilities include 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%). Competitive salary and benefits package offered.”
“ICON seeks a Project Administrative Assistant for COA licensing project coordination in Poland or Bulgaria. Role involves financial management, budget tracking, invoicing, and data verification. Requires 2+ years in project administration, strong Excel skills, and attention to detail. Competitive salary and benefits included.”
“Manager, Clinical Operations role at ICON, a global healthcare research organization. Oversees clinical trial execution, ensures compliance, and leads team coordination. Requires scientific degree, clinical operations experience, and leadership skills. 30% travel required. Competitive salary and benefits included.”
“ICON seeks a Manager, TMF Operations for a home-based role overseeing Trial Master File (TMF) compliance in clinical research. Requires GCP expertise, leadership in TMF management, and cross-functional collaboration. Competitive salary, benefits, and career development offered in a values-driven healthcare organization.”
“Project Manager position for Brazil at ICON, a global healthcare research organization. Remote role requiring strong project management skills, leadership, and stakeholder coordination. Competitive benefits package offered. Travel required (~30%).”
“Clinical Trial Coordinator role at ICON to facilitate clinical trial initiation, ensuring regulatory compliance and site activation. Requires life sciences degree, strong organizational skills, and occasional travel (5%). Competitive salary, benefits, and career development opportunities included.”
“Principal Engineer II role in Dublin for ICON, a healthcare intelligence company. Requires deep Linux expertise, IBM Spectrum Scale (GPFS), OpenShift/Kubernetes, VMware, and security hardening. Hybrid office role (60% attendance), with on-call duties. Competitive salary and benefits offered.”
“ICOM busca un Project Manager, Laboratory para coordinar estudios clínicos, gestionar 10-15 estudios bajo Buenas Prácticas Clínicas y actuar como enlace con patrocinadores. Requiere experiencia en gestión de proyectos en laboratorio o investigación clínica, comunicación sólida y manejo de múltiples prioridades. Ofrece salario competitivo y beneficios integrales.”
“Regulatory Technician role at ICON providing operational support for global regulatory submissions. Requires life sciences/pharmacy background, regulatory affairs experience, and strong organizational skills. Involves document preparation, maintenance of trackers, and quality checks. Offers competitive salary, benefits, and career development.”
“Senior Clinical Research Associate (CRA) role at ICON Plc to oversee clinical trial activities, ensure compliance with protocols and GCP standards, and manage site monitoring. Requires advanced degree in life sciences/nursing/medicine, extensive CRA experience, and 60% travel. Competitive salary, benefits, and career development included.”
“ICON seeks a Clinical Data Risk Analyst to assess and mitigate risks in clinical trial data, ensuring integrity and regulatory compliance. Requires expertise in statistical analysis, risk management, and strong collaboration skills. Offers competitive salary, benefits, and career development in a global healthcare research environment.”
“Clinical Research Associate (CRA II) position at ICON requiring 2+ years of monitoring experience. Responsibilities include site visits, data integrity, protocol compliance, and collaboration with investigators. Competitive salary, benefits, and travel (60%) required. Scientific/healthcare degree mandatory.”
“Clinical Research Associate (CRA) / Site Manager position in Breda for ICON, requiring Dutch and English fluency, experience in clinical trial monitoring, GCP/ICH knowledge, and hybrid work. Responsibilities include site management, trial coordination, and regulatory compliance.”
“Medical Admin Assistant I role at ICON for executive support and administrative tasks in clinical trials. Requires high school diploma, administrative experience, and proficiency in Microsoft Office Suite. Offers competitive salary, benefits, and career development opportunities.”
“ICON busca Project Manager para liderar proyectos en salud e investigación clínica, coordinando equipos, gestionando presupuestos, plazos y riesgos. Requiere experiencia en gestión de proyectos, liderazgo y herramientas como PMP/PRINCE2. Ofrece salario competitivo, beneficios integrales y oportunidades de desarrollo.”
“ICON seeks a Site Management Associate to support clinical trial site management, ensuring protocol compliance, GCP adherence, and operational efficiency. Requires a Bachelor's in life sciences/clinical research, site management experience, strong communication, and English proficiency. Offers competitive salary, benefits, and career development in a global healthcare research role.”
“Principal Auditor, Quality Assurance role at ICON for Mexico-based, fully remote position. Responsible for auditing CSV, AI/ML systems, and risk assessments in clinical trials. Requires expertise in GCP regulations, data integrity (ALCOA+), and regulatory inspections. Competitive salary and benefits included.”
“ICON seeks a Risk-Based Study Management Lead to oversee clinical study risks, ensuring patient safety and data quality. Role involves risk assessments, cross-functional meetings, and mitigation strategies. Requires clinical trial experience, ICH-GCP knowledge, and strong facilitation skills. Competitive benefits and UK-based remote work.”
“Contract Analyst role at ICON, a global healthcare research organization. Based in London with 1-day office presence. Responsibilities include contract management, invoicing, account reconciliation, and client relationship maintenance. Requires finance/accounting background, analytical skills, and experience in CRO/pharma/academia. Competitive salary and benefits package offered.”
“ICON seeks a Study Start Up Associate II to lead clinical trial initiation, ensuring regulatory compliance and managing submissions for ethics committees and agencies. Requires 2+ years in clinical research or regulatory affairs, life sciences degree, and occasional travel (5%). Competitive salary and benefits included.”
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