iconplc - IT - Administration

Join ICON plc as a Clinical Research Coordinator in Łódź. You will support clinical project execution, analyze data, and ensure operational success. We require a relevant degree, project experience, and strong analytical skills. Enjoy competitive benefits including health insurance and a global s...

Join ICON plc as a Clinical Research Associate in the United States. You will monitor clinical trial sites, ensure ICH-GCP compliance, and contribute to advancing treatments. This role requires 2+ years of CRA experience, strong organizational skills, and 60% travel. We offer competitive health i...

Join ICON plc as a Senior Clinical Research Associate in Ophthalmology. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and patient safety across multiple sites. This role requires extensive CRA experience, expertise in GCP, and 60% travel. We offer competitive hea...

Join ICON plc as a Senior Clinical Research Associate in Ophthalmology. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and patient safety across multiple sites. This role requires extensive CRA experience, strong monitoring skills, and 60% travel. We offer competi...

Join ICON plc as a Clinical Research Associate in the United States. You will monitor clinical trial sites, ensure protocol/GCP compliance, and manage data integrity. This role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer competitive health insurance, retiremen...

Join ICON plc as a Clinical Research Associate in Ophthalmology, based in the United States. You will monitor clinical trial sites, ensure ICH-GCP compliance, and contribute to advancing treatments. This role requires 2+ years of CRA experience, strong organizational skills, and 60% travel. We of...

Join ICON plc as a Clinical Research Associate II in a home-based role across Australia. Utilize your 2+ years of CRA experience and ICH-GCP knowledge to monitor sites and ensure data integrity in clinical trials. This pivotal role offers extensive travel, competitive benefits, and the chance to ...

Join ICON plc in Reading as a Senior Clinical Supplies Project Manager. Lead clinical supply projects, ensuring timely delivery for global trials. Utilize your 5+ years of supply chain experience to optimize processes and ensure regulatory compliance. Enjoy competitive benefits while shaping the ...

Join ICON plc, a global clinical research leader, as a Senior Clinical Research Associate in Kyiv. Oversee trial sites, ensure GCP compliance, and manage data integrity with 60% travel. Utilize your extensive CRA experience to drive study success within a supportive, innovative environment offeri...

Join ICON plc as a Global Delivery Manager and shape the future of clinical development. You will manage end-to-end clinical study delivery, ensuring quality, timelines, and budget. The role requires 5+ years in clinical research, strong ICH-GCP knowledge, and excellent project leadership. We off...

Join ICON plc in Beijing as a Clinical Research Associate II. You will design and analyze clinical trials, ensuring protocol compliance and data integrity. This role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer competitive health insurance, retirement planning,...

Join ICON plc, a global clinical research leader, as a Senior Clinical Research Associate. Oversee trial sites, ensure GCP compliance, and manage data integrity across multiple projects. This role requires extensive CRA experience, strong site management skills, and 60% travel. We offer competiti...