iconplc

Join ICON plc, a global clinical research leader, as a Clinical Research Associate II. You will monitor trial sites, ensure protocol/GCP compliance, and advance innovative therapies. This role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer competitive health insu...

Join ICON plc as a Clinical Research Associate II in Charlotte or Blue Bell. 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 ...

Join ICON plc as a Senior Clinical Research Associate in Utrecht. Oversee clinical trials, ensuring protocol adherence, data integrity, and GCP compliance. Requires extensive CRA experience, fluency in Dutch/English, and 60% travel. Enjoy health insurance, competitive retirement plans, and a glob...

Join ICON plc as a Senior Clinical Research Associate (CRA) in Houston, TX or St. Louis, MO. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. Requires 5+ years of CRA experience, including oncology monitoring, and 60% travel. We offer competitive...

Join ICON plc, a global clinical research leader, as a Clinical Research Associate II in Santiago, Chile. You will design trials, analyze complex medical data, and advance innovative therapies. The role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer competitive h...

Join ICON plc as a Clinical Research Associate II in Frankfurt. You will monitor clinical trial sites, ensure ICH-GCP compliance, and manage data integrity. This role requires 2+ years of CRA experience, fluency in English and German, and 60% travel. We offer competitive health insurance, retirem...

Join ICON plc, a global leader in clinical research, as a Clinical Site Associate in Warsaw. This hybrid role is key to ensuring site compliance and documentation accuracy for clinical trials. We seek a detail-oriented professional with a life sciences degree and strong organizational skills. Enj...

Join ICON plc as a Senior Clinical Research Associate in Oncology. Oversee clinical trials on the US West Coast, ensuring protocol compliance and data integrity. This role requires 5+ years of CRA experience with oncology monitoring and 60% travel. We offer competitive health insurance, retiremen...

Join ICON plc as a Senior Clinical Research Associate in Athens, Greece. Oversee oncology clinical trials, ensuring protocol adherence, data integrity, and GCP compliance. This role requires 12+ months of monitoring experience and offers extensive travel, competitive benefits, and a chance to sha...

Join ICON plc as a Senior Clinical Research Associate in Bangkok. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. This role requires extensive CRA experience, strong site management skills, and 60% travel. We offer competitive health insurance, ...

Join ICON plc as a Clinical Site Associate in Milan, Italy. Support clinical trial operations by ensuring site compliance, documentation accuracy, and audit readiness. Requires a life sciences degree, clinical research experience, and fluency in Italian and English. Enjoy competitive benefits inc...

Join ICON plc in Mexico City as a Study Start-Up Associate II. Utilize your 2-4 years of clinical start-up experience and regulatory knowledge to support site activation and submissions. This role offers competitive benefits, including health insurance and retirement planning, in a global leader ...