iconplc - Remote work

Join ICON plc as a Clinical Research Associate II in Utrecht. You will monitor clinical trial sites, ensure protocol/GCP compliance, and manage data integrity. Requires 2+ years CRA experience, fluency in Dutch/English, and 60% travel. We offer competitive health insurance and retirement plans.

Join ICON plc, a global clinical research leader, as a Clinical Research Associate II in Santiago, Chile. You will monitor sites, ensure protocol/GCP compliance, and contribute to advancing innovative therapies. This role requires 2+ years of CRA experience, strong organizational skills, and 60% ...

Join ICON plc as a Senior Clinical Research Associate in Oncology. Based in Los Angeles, you will oversee clinical trials, ensuring protocol adherence and data integrity. This role requires 5+ years of CRA experience with oncology monitoring and 60% travel. We offer competitive health insurance a...

Join ICON plc as a Senior Clinical Research Associate in Frankfurt. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. Requires extensive CRA experience, fluency in English and German, and 60% travel. Enjoy competitive benefits including health ins...

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