iconplc - IT - Administration

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 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 ...

Join ICON plc as a Clinical Trial Assistant in Blue Bell, US. Support the design and analysis of clinical trials, managing documentation and ensuring regulatory compliance. This role requires a scientific degree, knowledge of trial processes, and strong organizational skills. We offer competitive...

Join ICON plc's collaborative Biotech team as a Senior CRA or CRA II. This remote role based in the Netherlands involves independently monitoring Phase II-IV trials for biotech sponsors. Requires a life science degree, monitoring experience, and fluency in Dutch/English. We offer competitive bene...

Lead early-phase clinical trials as a Global Trial Manager with ICON plc. This role requires 4+ years of experience overseeing Phase I studies and vendor management. You will ensure operational excellence and compliance with ICH/GCP guidelines. The position offers competitive benefits and is base...