iconplc - IT - Administration

Join ICON plc as a Senior Clinical Research Associate in Sofia. You will manage Phase I-IV site monitoring and ensure regulatory compliance for a leading biopharma in cutting-edge therapies. This sponsor-dedicated role requires 3.5+ years of independent monitoring experience. We offer competitive...

Join ICON plc as a Senior Clinical Research Associate or CRA II in the United States. You will design and analyze clinical trials, ensure protocol compliance, and monitor sites with 60% travel. We require a scientific degree, 1-3+ years of independent monitoring experience, and ICH-GCP knowledge....

Join ICON plc as a Clinical Research Associate II in Wuhan, China. 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 plan...

Join ICON plc as a Clinical Research Associate II in Guangzhou. 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, retirement pla...

Join ICON plc in Shanghai as a Clinical Research Associate II. You will monitor clinical trial sites, ensure protocol/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 in...

Join ICON plc as a Clinical Research Associate II in Seoul. You will monitor global oncology trials, ensuring protocol compliance and data integrity with 60% travel. We require 2+ years of CRA experience, ICH-GCP knowledge, and SIT on-site monitoring expertise. Enjoy competitive health insurance,...

Join ICON plc, a global clinical research leader, in Seoul as a Senior Clinical Trial Associate. Utilize your CTA/CRA experience to manage essential documents, IMP, and safety data within our MAP programs. We seek a detail-oriented professional with strong communication skills and knowledge of tr...

Lead and manage early-phase oncology clinical trials from planning through execution. This role requires strong ICH/GCP knowledge, Phase I oncology experience, and global vendor management skills. We offer a competitive benefits package including health insurance and retirement planning. This pos...

Join ICON plc as a Clinical Site Associate (In-House CRA) in Hong Kong. Support clinical trial operations, ensuring site compliance and documentation accuracy in this hybrid office role. Utilize your life sciences background and organizational skills within a world-leading CRO. Enjoy competitive ...

Join ICON plc in Nanjing as a Clinical Research Associate II. Utilize your 2+ years of CRA experience and ICH-GCP knowledge to monitor sites and ensure data integrity in global clinical trials. This role offers significant travel, competitive benefits, and a chance to shape the future of clinical...

Join our Integrated Data Analytics team in Johannesburg as an Analytical Monitor. You will support global clinical trials through data analysis, early risk identification, and delivering insights for site managers. The role requires 2+ years' clinical research experience, strong analytical skills...

Join ICON plc as a Clinical Research Associate II in Kuala Lumpur. 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, retirement ...