iconplc - IT - Administration

Join ICON plc as a Senior Clinical Research Associate in Basel. Oversee clinical trials, ensuring protocol adherence, data integrity, and GCP compliance across multiple sites. Requires extensive CRA experience, fluency in English, German, and French, and 60% travel. We offer competitive health in...

Join ICON plc as a Senior Clinical Research Associate in Ankara. Oversee clinical trials, 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, retirement ...

Join ICON plc as a Senior Clinical Research Associate in São Paulo. Oversee clinical trials, ensuring protocol adherence, data integrity, and GCP compliance. Requires extensive CRA experience, strong English, and 60% travel. We offer competitive health insurance, retirement plans, and global supp...

Lead global clinical trial site activation as a Project Manager, ensuring timely, budget-conscious, and high-quality delivery. Utilize your 3-6 years of startup experience and regulatory knowledge to coordinate all activation activities. This role offers competitive benefits, including health ins...

Join ICON plc as a Clinical Research Associate II in Frankfurt. You will monitor clinical trial sites, ensure ICH-GCP compliance, and contribute to advancing treatments. The role requires 2+ years of CRA experience, fluency in English and German, and 60% travel. We offer competitive health insura...

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...