“Contrato de asociado en gestión de contratos para ICON, empresa de investigación clínica y salud. Requiere experiencia en gestión contractual, negociación y cumplimiento normativo. Posición remota en España con beneficios competitivos, viajes ocasionales (5%) y oportunidades de desarrollo profesional.”
Icon plc | Von zu Hause aus |Graduate Programme, Medizin, Englisch
“Graduate Pharmacovigilance Associate role at ICON for remote work in Poland. Requires a Bachelor's degree in pharmacy/life sciences, attention to detail, and pharmacovigilance knowledge. Involves adverse event data processing, safety report submission, and cross-functional collaboration. Competitive benefits and inclusive workplace culture offered.”
“Regular job offer for an Investigator Payments Coordinator at ICON, a global clinical research organization. Responsible for managing and processing payments to clinical trial investigators, ensuring accuracy, compliance, and timely financial transactions. Requires 2+ years of financial coordination experience, preferably in clinical research, with strong attention to detail and communication skills.”
“Regular job offer for a Site Activation Partner at ICON, a global healthcare organization. Responsibilities include facilitating clinical trial initiation, regulatory compliance, and stakeholder coordination. Requires a Bachelor's degree in life sciences, strong organizational skills, and occasional travel (5%). Competitive salary and benefits package included.”
“Offer for a Clinical Research Associate II position in Romania, requiring 2+ years of experience. Responsibilities include clinical trial monitoring, site visits (60% travel), data integrity, and protocol compliance. Office presence in Bucharest 2-3 times weekly. Competitive salary and benefits package included.”
“Site Contracts Negotiator II role at ICON for negotiating clinical trial agreements and budgets with investigator sites. Requires contract management experience, negotiation skills, and collaboration with legal/finance teams. Offers competitive salary, benefits, and career development in healthcare CRO.”
“TMF Lead position in Mexico City (hybrid role) at ICON, a healthcare research organization. Oversees Trial Master File management, ensures regulatory compliance, and collaborates with cross-functional teams. Requires TMF experience, life sciences degree, and office presence 3x/week. Offers competitive salary and benefits.”
“ICON seeks a Clinical Supplies Project Manager to design clinical trials, manage drug supply planning, and interpret medical data. Requires 4+ years in clinical supplies, project management skills, and proficiency in IRT systems. Position is fully remote with competitive salary, benefits, and career development opportunities.”
“Manager, Clinical Operations role in Germany for ICON, overseeing clinical trial execution, ensuring compliance, and leading cross-functional teams. Requires scientific/healthcare degree, clinical ops experience, German/English fluency, and 30% travel. Competitive salary, benefits, and career development included.”
“Permanente Position als Clinical Site Associate in Deutschland bei ICON. Verantwortlich für Site-Aktivitäten, Dokumentenmanagement, CRF-Kommunikation und Compliance in klinischen Studien. Erfordert Bachelor in Life Sciences, Deutsch- und Englischkenntnisse sowie Reisebereitschaft (ca. 10%). Attraktives Gehaltspaket und Benefits.”
“Site Payment Specialist (hybrid) en Roumanie, Serbie ou Croatie chez ICON pour gérer les paiements des sites cliniques, assurer la conformité réglementaire et superviser les aspects financiers des essais cliniques. Expérience requise en paiements, maîtrise d'Excel et logiciels financiers. Salaire compétitif et avantages sociaux inclus.”
“ICON seeks a Clinical Trial Manager II to design and analyze clinical trials, interpret medical data, and oversee trial operations. Requires a relevant Bachelor's degree, clinical trial management experience, and 25% travel. Competitive salary, benefits, and career development opportunities included.”
“Global Data Manager role at ICON for leading clinical data science workstreams, ensuring quality and compliance in clinical trials. Requires strong leadership, data analysis expertise, and cross-functional collaboration. Offers competitive salary, benefits, and remote work.”
“ICON seeks a Clinical System Lead to oversee clinical trial systems (CDMS) setup, maintenance, and team leadership. Role involves technical project management, peer reviews, client interactions, and revenue forecasting. Requires 2+ years in clinical data management, strong leadership, and expertise in relational databases and agile project management. Competitive salary and benefits 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, and coordinating with stakeholders. Requires a Bachelor's degree in life sciences, fluency in German and English, and occasional travel. Competitive benefits package included.”
“Home-based Clinical Trial Liaison role requiring trilingual fluency (Spanish, Portuguese, English) and up to 75% travel. Doctoral degree (M.D., PharmD, or PhD) required. Responsible for site recruitment, trial design, and stakeholder communication in clinical research environment.”
“Site Payment Specialist role at ICON for clinical trials in Sofia, Bulgaria. Hybrid position requiring finance/accounting background with 1+ year in payments. Duties include managing site payments, ensuring compliance, and coordinating with cross-functional teams. Competitive benefits package offered.”
“Oferta de empleo como Site Management Associate II en ICON para gestionar y supervisar ensayos clínicos en Polonia y Bulgaria. Requiere grado en ciencias de la vida o similar, experiencia en investigación clínica, dominio de inglés y español, y conocimientos de GCP. Ofrece salario competitivo y beneficios.”
“Oferta de empleo en Ciudad de México para el puesto de Site Management Associate I en ICON, organización global de investigación clínica. Requiere título universitario en ciencias de la vida o áreas afines, 2+ años de experiencia en investigación clínica y conocimiento de GCP. Rol administrativo y operativo en apoyo a ensayos clínicos, gestión de documentación TMF y coordinación con equipos multidisciplinarios. Posición presencial.”
“Offre d'emploi pour un Clinical Site Associate (CSA) à Paris, France. Poste initialement en bureau avec évolution vers un rôle de CRA voyageant sous un an. Missions : support aux sites cliniques, gestion de la documentation, conformité et préparation aux audits. Profil recherché : expérience en recherche clinique, maîtrise du français et de l'anglais, connaissance des réglementations ICH-GCP.”
“ICON seeks a UK-based Clinical Research Associate (CRA) for remote clinical trial monitoring. Role involves coordinating study setup, ensuring compliance with ICH-GCP, maintaining documentation, and collaborating with stakeholders. Requires a science/medicine degree, travel (~40%), and strong communication skills. Competitive salary, benefits, and career development offered.”
“ICON seeks an IT Product Manager in Dublin, Ireland for a hybrid role (60% office-based). Responsibilities include defining IT products, partnering with business/tech teams, and driving lifecycle management. Requires strong product lifecycle knowledge, stakeholder collaboration, and problem-solving skills. Competitive salary and benefits included.”
“Regular job offer for a Study Start Up Associate I role at ICON, a global clinical research organization. Responsibilities include site start-up, qualification, training coordination, and site management for clinical trials. Requires strong communication skills, GCP compliance, and database management. Competitive salary, benefits, and career development opportunities included.”
“ICON seeks a Project Manager for Post Trial Access (PTA) programs in clinical research. Role involves leading global PTA programs, managing timelines/budgets, coordinating cross-functional teams, and ensuring regulatory compliance for investigational products prior to approval. Requires 2+ years in PTA or expanded access programs, strong project management, and stakeholder collaboration. Fully remote position with competitive benefits.”
“Puesto como CRA II en Argentina para ICON, organización global en investigación clínica. Requiere título en ciencias de la salud y 2+ años de experiencia en monitoreo de ensayos clínicos. Viajes frecuentes (60%), conocimiento en ICH-GCP y protocolos. Salario competitivo y beneficios integrales.”
“Global Study Manager role at ICON for Clinical Trial Management II, overseeing trials, analyzing data, and ensuring regulatory compliance. Requires clinical trial experience, strong analytical skills, and 25% travel. Competitive salary, benefits, and career development offered.”
“Payment Specialist role at ICON for processing investigator payments in clinical trials, ensuring regulatory compliance (e.g., Sunshine Act, FMV). Requires 1-2 years in finance/accounting, preferably in pharmaceutical/clinical research. Competitive salary, benefits, and career development opportunities included.”
“Regular job offer for a Lab Analyst I position in the QC Laboratory in Assen, Netherlands. Requires a Bachelor's degree in biology, chemistry, or a related field, 0-2 years of experience, and skills in laboratory testing, data recording, and equipment maintenance. ICON offers a competitive salary, benefits, and career development opportunities.”
“Regular job offer for a Site Services Specialist I at ICON, supporting clinical trial sites with logistics, issue resolution, and compliance. Requires a bachelor's degree in life sciences/healthcare and clinical research experience. Competitive salary, benefits, and travel (1%).”
“Central Review Coordinator role at ICON in Mexico for clinical trial data coordination. Requires life sciences/computer science degree, clinical research experience, and strong project management skills. Focus on centralized review activities, data integrity, and cross-functional collaboration. Competitive salary, benefits, and inclusive workplace culture.”
“ICON recrute un Clinical Research Associate (CRA) pour superviser des essais cliniques, assurer la conformité réglementaire (ICH-GCP), coordonner les études et maintenir les documents. Poste basé en présentiel avec 60% de déplacements. Salaire compétitif et avantages sociaux complets. Profil : diplôme en médecine/sciences, expérience en monitoring clinique et excellente communication en anglais.”
“Oferta de empleo en Ciudad de México para el puesto de Site Management Associate II en ICON, organización global de investigación clínica. Requiere experiencia en administración de ensayos clínicos, gestión de TMF y conocimiento de GCP. Rol administrativo y operativo en apoyo a equipos de investigación clínica, sin interacción directa con sitios. Ofrece salario competitivo y beneficios.”
“Senior Clinical Research Associate (CRA) position at ICON Plc for monitoring clinical trials, ensuring protocol and regulatory compliance. Requires Bachelor's in relevant field, extensive CRA experience, and 60% travel. Competitive salary, benefits, and career development offered.”
“ICON Plc busca un Study Delivery Manager en Guatemala para liderar la planificación, ejecución y finalización de ensayos clínicos, asegurando cumplimiento de plazos, presupuestos y regulaciones. Requiere título universitario en medicina o ciencias, experiencia en monitoreo y capacidad para viajar hasta un 20%. Ofrece salario competitivo, beneficios integrales y oportunidades de desarrollo profesional.”
“Senior Clinical Trial Manager position at ICON for Brazil-based remote work. Requires 2+ years in CRA/CTM roles, budget oversight, study start-up, and stakeholder management. Offers competitive salary, health benefits, and career development in clinical research.”
“ICON busca un Clinical Research Associate en Belém do Pará para diseñar y analizar ensayos clínicos, garantizar cumplimiento de protocolos, integridad de datos y seguridad del paciente. Requiere experiencia en CROs o farmacéuticas, conocimiento de ICH-GCP y habilidades organizacionales. Ofrece salario competitivo, beneficios de salud, planes de jubilación y desarrollo profesional.”
“Principal Safety Scientist role at ICON requiring strong pharmacovigilance experience in Bulgaria or Poland. Leads safety assessments, pharmacovigilance activities, and regulatory submissions. Requires scientific expertise, team leadership, and regulatory compliance knowledge. Offers competitive salary, benefits, and career development.”
“ICON seeks a Site Budgeting and Contracting Specialist to manage contract analysis, invoicing, and financial reporting for assigned accounts. Requires a Bachelor's in Finance/Accounting, contract management experience, and strong analytical skills. Competitive salary, benefits, and career development opportunities included.”
“Oferta de empleo para Asistente Administrativo de Estudios Clínicos Nivel 1 en CDMX, con modalidad home based. Requiere experiencia en apoyo ejecutivo, manejo de información confidencial, organización de agendas y viajes, dominio de Office y habilidades comunicativas. Incluye paquete de beneficios competitivo y oportunidades de desarrollo.”
“ICON seeks an HR Technology Lead with extensive Workday and HRIS experience to oversee HR tech strategy, implementation, and governance. Role involves managing L2/L3 Workday cases, leading functional teams, and ensuring HRIS compliance. Competitive salary and benefits package offered. Must have legal right to work in UK/Ireland.”
“Pharmacovigilance Project Lead role in Bulgaria requiring solid experience in pharmacovigilance and drug safety. Oversees safety monitoring, adverse event reporting, and regulatory compliance for clinical trials and post-marketing activities. Requires leadership, project management, and cross-functional team coordination. Competitive salary and benefits included.”
“Site Contracts Negotiator II role at ICON in Sofia, Bulgaria, for negotiating and executing clinical trial agreements and budgets. Requires law/business/life sciences degree, fluency in English and Bulgarian/Czech/Portuguese, and experience in site contracting or healthcare CRO. Remote or office-based position with competitive benefits.”
“ICON plc busca un Pathology Project Manager en Dublín (modalidad híbrida) para gestionar proyectos de patología digital, coordinar equipos de histopatólogos y proveedores externos, y garantizar cumplimiento normativo. Requiere título universitario y 3+ años en gestión de proyectos farmacéuticos/CRO. Ofrece paquete competitivo de beneficios y desarrollo profesional.”
“Oferta de empleo como Asistente Administrativo Senior en ICON, organización global de investigación clínica. Trabajo remoto en CDMX. Requiere experiencia en apoyo ejecutivo, manejo de agendas complejas, confidencialidad y dominio de Office. Ofrece paquete competitivo de beneficios y oportunidades de desarrollo.”
“Principal Auditor role in Quality Assurance at ICON, hybrid in Reading (UK) or Dublin (Ireland). Responsible for auditing AI/ML systems, CSV, data integrity (ALCOA+), and regulatory compliance. Requires expertise in GxP regulations, risk assessment, and stakeholder management. Competitive salary and benefits included.”
“Oferta de emprego remoto para Site Contracts Negotiator II no Brasil, focada na negociação e gestão de contratos e orçamentos de estudos clínicos com centros de investigação. Requer experiência em contratos de CRO/Pharma, formação em direito, negócios ou ciências da vida, e habilidades de negociação e organização. Inclui benefícios competitivos e salário base.”
“ICON seeks a Statistical Programmer II to develop, validate, and maintain R-based statistical programs for clinical trials, ensuring data integrity and regulatory compliance. Role involves collaborating with biostatisticians, mentoring junior programmers, and translating study requirements into actionable insights. Requires 3+ years of R experience in clinical research and a degree in statistics or related field.”
“ICON seeks a Principal Biostatistician to lead clinical trial design, data analysis, and regulatory interactions. Requires 7-9+ years in biostatistics (Ph.D/Master's), expertise in drug development, and strong leadership. Offers competitive salary, benefits, and career growth in a global healthcare research role.”
“ICON busca un Project Manager para liderar proyectos en salud e investigación clínica, coordinando equipos, plazos y presupuestos. Requiere experiencia en gestión de proyectos, liderazgo y herramientas como PMP/PRINCE2. Ofrece salario competitivo, beneficios de salud, desarrollo profesional y modalidad remota.”
“Clinical Research Associate (CRA1/CRA2) position in São Paulo to monitor clinical trials, ensuring compliance with ICH-GCP and regulatory requirements. Requires degree in medicine/science, 60% travel, strong communication skills, and experience in clinical trial operations. Competitive salary, benefits, and career development included.”
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