iconplc - Hybrid work

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...

Join ICON plc as a Clinical Research Associate II in Puerto Rico. 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...

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, 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...