iconplc - IT - Administration

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 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 and English, and 60% travel. Enjoy competitive benefits including health insurance and...

Join ICON plc as a Senior Validation Engineer in Blue Bell, PA or Raleigh, NC. This office-based role with remote flexibility requires 10+ years of CSV/GxP experience. You will lead validation for complex global projects, ensuring compliance with FDA and EMA regulations. We offer competitive heal...

Lead clinical trials from planning to execution in Taipei, Taiwan. This pivotal role requires extensive operations management experience and strong leadership skills to ensure regulatory compliance and trial efficiency. You will mentor teams and drive innovation in a world-leading clinical resear...