iconplc - IT - Software Development

Principal CRA opportunity with ICON plc, home-based in Mexico. Lead complex clinical trials, mentor CRAs, and ensure ICH-GCP compliance across site management activities. Requires a Bachelor’s in a scientific field, extensive CRO/pharma experience, and strong leadership skills. Enjoy competitive ...

Senior Clinical Research Associate sought by ICON plc in Paris, France. This role involves overseeing global clinical trials, ensuring GCP compliance, data integrity, and patient safety. Requires extensive CRA experience, strong site management skills, and 60% travel. Join a world-leading healthc...

ICON seeks a Clinical Research Associate II in Shenyang, China, to design and analyze clinical trials, ensuring protocol compliance and patient safety. Requires a Bachelor’s in science/healthcare and 2+ years of CRA experience with ICH-GCP knowledge. You will conduct site visits, manage data inte...

ICON seeks a Clinical Research Associate II in Hangzhou, China, to design and analyze clinical trials. You will ensure protocol compliance, data integrity, and patient safety while conducting site visits. Requires a Bachelor’s degree, 2+ years of CRA experience, and ICH-GCP knowledge. Benefits in...

Principal Programmer role in Bucharest, Romania, embedded within a top pharmaceutical organization. Lead complex clinical data analysis using R, mentor programming teams, and drive high-quality, reproducible outputs for regulatory submissions. Requires significant statistical programming experien...

Join ICON plc as a Clinical Data Coordinator I in Warsaw, Poland. You will design and analyze clinical trials, interpret medical data, and support innovative treatments. Requires a Master’s in Life Sciences or Healthcare, basic clinical data management knowledge, and familiarity with Medidata or ...