iconplc

Join ICON as a Senior Clinical Data Science Programmer in Bangalore. Utilize your SAS/R/Python expertise to develop programming solutions for clinical trial data analysis and reporting. Collaborate cross-functionally to ensure data accuracy and support innovative therapies. Enjoy competitive bene...

Lead regulatory submissions (CTA/IND/MAA) for a global pharmaceutical sponsor in this home-based role in Australia. Leverage 6+ years of pharmaceutical regulatory affairs experience to provide strategic guidance and lead internal teams. Enjoy a competitive package with health insurance and a supp...

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 in the United States. You will monitor clinical trial sites, ensure ICH-GCP compliance, and contribute to advancing innovative therapies. This role requires 2+ years of CRA experience, strong organizational skills, and 60% travel. We offer competitiv...

Join ICON plc as a Clinical Research Associate II or Senior in São Paulo. You will conduct site monitoring visits, ensure protocol/GCP compliance, and contribute to trials in key therapeutic areas. This role requires a science degree, CRA experience, 70% travel, and advanced English. We offer com...