10,000+ employees
Founded 1990
💼 Consulting
🏥 Healthcare
📦 Logistics
Consulting • Healthcare • 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.
🔥 0 minutes ago
🌐 United States, United Kingdom, +1 more countries – Remote
🔔 Pennsylvania – Remote
⏰ Full Time
🟠 Senior
👻 Ghost score 10%
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10,000+ employees
Founded 1990
💼 Consulting
🏥 Healthcare
📦 Logistics
Consulting • Healthcare • 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.
• Provide senior medical and radiology leadership for sponsor studies, including imaging strategy, protocol design, imaging manuals, read methodology, charters, system requirements, training materials, quality control and independent reviewer processes • Partner with Business Development and operational teams on new business opportunities, bid defenses, capabilities meetings and client relationship development • Represent ICON’s medical, scientific and imaging expertise in internal and external discussions • Support responses to requests for proposals and information with scientific, medical and technical input • Provide real-time consultation on imaging-related scientific and operational questions, including protocol development, radiology case review, contrast use, imaging analysis, read design, read criteria and issue resolution • Build trusted client relationships by advising on imaging strategy and supporting regulatory authority responses • Supervise independent read teams, including reader training, Q&A, performance monitoring, inter-reader variability assessment, retraining plans and read-quality oversight • Oversee imaging reads and provide medical review and guidance • Participate in industry forums, imaging standardization initiatives, scientific meetings and external presentations • Mentor medical, scientific and operational colleagues • Lead, motivate and advise project and study teams • Guide medical and scientific activities for timely, complete and client-focused delivery • Develop capability across medical, scientific and operations teams by translating complex concepts into practical study guidance
• MD with fellowship training in radiology is required • Additional training or demonstrated experience supporting clinical research is strongly preferred • Expertise in neuroradiology and body imaging is strongly preferred • Cross-certification in nuclear medicine is preferred • Deep expertise in imaging endpoints for clinical trials • Comprehensive knowledge of drug development, biomarker development, adaptive design, regulatory submission and post-marketing studies • Strong working knowledge of applicable regulatory expectations, including ICH-GCP and relevant regional requirements • Demonstrated ability to lead complex, large-scale projects and influence through scientific credibility, sound judgment and effective stakeholder engagement • Excellent communication and presentation skills • Ability to advise clients, support business development activities and represent ICON in public or scientific forums • Live in the US, UK, or Ireland • Ability to travel up to 10% • Legal right to work in the country where the role is based
• Competitive base salary and performance related incentives • Health and wellbeing programmes including medical, dental, and vision coverage where applicable • Retirement and pension plans • Life assurance and disability coverage • Employee assistance programmes and wellbeing resources • Learning and development opportunities through structured training and career pathways
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