10,000+ employees
Founded 1990
đŒ Consulting
đ„ Healthcare
đŠ Logistics
Consulting âą Healthcare âą Logistics
ICON plc is a global provider of clinical, consulting, and commercial services across various sectors in the healthcare and pharmaceutical industries. They offer a wide range of clinical solutions, including decentralised clinical trials, cardiac safety solutions, early clinical laboratories, and medical imaging. ICON also provides technology solutions that support drug development from early phases to post-marketing. Their therapeutic expertise spans cardiovascular, oncology, internal medicine, and more, with a strong focus on transformative therapies like cell and gene therapies and biosimilars. ICON is recognized as a leading Contract Research Organisation (CRO), regularly providing thought leadership and contributing to industry publications and events. Their services are tailored to optimize clinical trials, offer regulatory intelligence, and deliver real-world evidence through robust data analysis and patient-centric solutions.
Selected: đ Date Added.
đ 2 days ago
Director managing strategic partnership infrastructure, governance, and optimization for ICON, a global healthcare intelligence and clinical research organisation. Leading cross-functional implementation, stakeholder engagement, and continuous improvement.
đ 2 days ago
Senior Regulatory Affairs Specialist developing global regulatory strategies for ICON, a healthcare intelligence and clinical research organisation. Managing submissions, health-authority interactions, and compliance across drug development.
đ 2 days ago
AI Engineer developing Python, AWS, and knowledge-graph solutions for ICONâs clinical trial data analysis. Supporting statistical programming, reporting, and regulatory-compliant deliverables.
đ Ireland, France, +6 more countries â Remote
â° Full Time
đĄ Mid-level
đ Senior
đ€ AI Engineer
đ» Ghost score 10%
đ 2 days ago
Clinical Research Associate monitoring medical-device clinical trials for ICON Strategic Solutions. Verifying site compliance, source data, reporting, and regulatory documentation across Boston, Philadelphia, or Dallas.
đ Massachusetts, Pennsylvania, +1 more states â Remote
â° Full Time
đą Junior
đĄ Mid-level
đ§Ș Clinical Research
đ» Ghost score 10%
đ 2 days ago
Senior Medical Writer leading clinical document development and regulatory submissions at ICON Strategic Solutions. Supporting sponsor-dedicated research programs advancing innovative treatments.
đ 2 days ago
Senior Site Partner strengthening investigator-site relationships for ICON, a global healthcare intelligence and clinical research organization. Improving study performance, recruitment, quality, and site engagement.
đ 2 days ago
Remote Clinical Research Associate monitoring sponsor-dedicated cardio and obesity trials for ICON Strategic Solutions. Conducting site visits, ensuring protocol compliance, and maintaining clinical data integrity.
đ Florida â Remote
â° Full Time
đą Junior
đĄ Mid-level
đ§Ș Clinical Research
đ» Ghost score 10%
đ 2 days ago
Clinical Research Associate monitoring sponsor-dedicated cardio and obesity trials for ICON. Ensuring compliant site conduct, data integrity, and patient safety.
đ Florida â Remote
â° Full Time
đą Junior
đĄ Mid-level
đ§Ș Clinical Research
đ» Ghost score 10%
đ 2 days ago
Clinical Research Associate monitoring sponsor-dedicated cardio and obesity trials for ICON Strategic Solutions. Conducting site visits, ensuring ICH-GCP compliance, and maintaining clinical data integrity.
đ€ Texas â Remote
â° Full Time
đą Junior
đĄ Mid-level
đ§Ș Clinical Research
đ» Ghost score 10%
đ 2 days ago
Remote Clinical Research Associate monitoring sponsor-dedicated cardio and obesity trials for ICON Strategic Solutions. Conducting site visits, ensuring ICH-GCP compliance, and maintaining clinical data integrity.
đ Florida, Texas â Remote
â° Full Time
đą Junior
đĄ Mid-level
đ§Ș Clinical Research
đ» Ghost score 10%
đ 3 days ago
Clinical Trial Associate supporting clinical trial administration and regulatory documentation at ICON Strategic Solutions. Tracking study progress and coordinating sites, stakeholders, and cross-functional teams.
đŹđ· Greece â Remote
â° Full Time
đą Junior
đĄ Mid-level
âš Clinical Trial Associate
đ» Ghost score 10%
đ 3 days ago
Global Study Associate Director leading cardiovascular and cardiometabolic clinical trials for ICON, a global clinical research organisation. Driving study execution, budgets, vendors, timelines, and cross-functional teams.
đ 3 days ago
Site Engagement Manager supporting ICONâs global clinical trials through investigator and research-site engagement. Improving site performance, recruitment, and timely trial delivery across UK hospital sites.
đŹđ§ United Kingdom â Remote
â° Full Time
đĄ Mid-level
đ Senior
đ Manager
đ» Ghost score 10%
đ 3 days ago
Senior Grants Specialist overseeing grant lifecycles, compliance, reporting, and funding strategy. Supporting ICONâs sponsor-dedicated clinical research services through expert grant administration.
đ 3 days ago
Senior CRA monitoring clinical trials for ICONâs sponsor-dedicated research programs. Ensuring protocol compliance, site performance, data integrity, and GCP standards across Greece.
đ 3 days ago
Senior Clinical Research Associate overseeing site monitoring and compliance for ICONâs sponsor-dedicated clinical trials. Supporting data integrity, site performance, and successful trial execution.
đŁïžđ©đȘ German Required
đ 3 days ago
Clinical Research Associate II monitoring clinical trials for ICONâs sponsor-dedicated research programs. Ensuring protocol compliance, data integrity, and patient safety across study sites.
đ”đč Portugal â Remote
â° Full Time
đą Junior
đĄ Mid-level
đ§Ș Clinical Research
đ» Ghost score 10%
đ 3 days ago
Senior Clinical Research Associate monitoring clinical trial sites for ICON in Milan, Italy. Ensuring protocol compliance, data integrity, and successful sponsor-dedicated trial execution.
đźđč Italy â Remote
đ” âŹ45k - âŹ56.3k / year
â° Full Time
đ Senior
đ§Ș Clinical Research
đ» Ghost score 0%
đ 3 days ago
Remote CRA II monitoring clinical trials for ICONâs sponsor-dedicated research programs. Ensuring protocol compliance, data integrity, and patient safety across Malaysian sites.
đČđŸ Malaysia â Remote
â° Full Time
đą Junior
đĄ Mid-level
đ§Ș Clinical Research
đ» Ghost score 10%
đ 3 days ago
Clinical Trial Associate supporting clinical trial coordination, documentation, and regulatory compliance at ICON. Contributing to sponsor-dedicated research advancing innovative treatments.
đČđŸ Malaysia â Remote
â° Full Time
đą Junior
đĄ Mid-level
âš Clinical Trial Associate
đ» Ghost score 10%
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