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.
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Principal Clinical Data Standards Consultant at ICON focusing on data management standards and compliance in clinical research. Collaborating with teams to enhance data collection processes and mentor junior staff.
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As a Clinical Data Science Associate at ICON, you will analyze clinical trial data and provide insights. Collaborating with teams to ensure data integrity and improve analysis processes.
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Senior Clinical Research Coordinator managing a Hypersomnolence Study for ICON. Overseeing clinical coordination and ensuring efficient study conduct within a pharmaceutical company.
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Clinical Trial Manager leading operational delivery of oncology clinical studies for ICON. Collaborating with cross-functional teams to ensure successful execution of complex oncology programmes while maintaining high standards.
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Clinical Associate supporting the design, implementation, and management of clinical trials to advance new therapies. Collaborating with cross-functional teams to ensure compliance and accuracy in clinical studies.
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Site Contract Manager at ICON preparing and executing invoicing for healthcare intelligence and clinical research organization. Balancing client relationships and ensuring timely billing for assigned accounts.
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Clinical Research Associate ensuring site compliance and data integrity across multiple therapeutic areas. Conducting site visits and supporting clinical study operations in the West Region.
🌵 Arizona, California, +2 more states – Remote
💵 $91.3k - $114.2k / year
⏰ Full Time
🟢 Junior
🟡 Mid-level
🔬 Research Analyst
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Manage clinical trial operations at ICON, a global healthcare intelligence and clinical research organisation. Supporting teams to deliver high-quality outcomes across clinical programmes.
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Project Manager in clinical research overseeing 10-15 studies at ICON. Managing client relationships and ensuring study compliance with regulatory standards.
🕒 2 days ago
Senior Clinical Research Associate managing clinical trial activities ensuring data integrity and participant safety. Overseeing site performance, compliance, and training for regulatory adherence at ICON Plc.
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Quality Assurance Manager at ICON overseeing quality and compliance in clinical trials. Collaborating with project teams and implementing strategies to address quality issues.
Google Cloud Platform
🕒 2 days ago
Clinical Trial Associate role at ICON focusing on coordinating clinical trials and regulatory compliance. Collaborating with teams to manage clinical trial documentation and metrics effectively.
🗣️🇨🇿 Czech Required
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Manager of quality assurance at ICON ensuring quality and compliance of clinical trials. Developing quality assurance strategies and collaborating with project teams to resolve quality issues.
Google Cloud Platform
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Clinical Research Associate monitoring clinical trials and ensuring compliance for a global healthcare organization. Collaborating with investigators to ensure high-quality data and patient safety.
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Laboratory Study Manager at ICON, focusing on clinical trial management, oversight, and compliance. Collaborating with teams to implement clinical studies effectively while ensuring data integrity.
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Clinical Trial Manager at ICON managing clinical trial operations and team engagement for high-quality outcomes. Overseeing budgets, study plans, and ensuring effective partnerships among stakeholders.
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Clinical Trial Liaison designing and analyzing clinical trials at ICON. Collaborating with teams to enhance patient recruitment and retention while ensuring regulatory compliance.
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Study Start-Up Associate II supporting site start-up and communication within clinical research organization. Collaborating with teams for documentation and site activation timelines.
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Clinical Registry Coordinator at ICON ensuring transparency and integrity of clinical trial data and results. Responsible for managing clinical registry support and documentation.
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Global Study Associate supporting the Global Study Director and Managers in clinical research. Leading eTMF setup, document management, and compliance in a collaborative environment.
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