Search the 2 jobs at ICON plc

As a Clinical Research Associate II, you will conduct monitoring and management of clinical trials, ensure compliance with protocols, collaborate with site staff, and review data for integrity and quality.

As a Clinical Research Associate II at ICON, you will conduct site visits for clinical trials, ensure protocol compliance, and collaborate with investigators. Your role will involve data review, query resolution, and preparation of study documentation, contributing to the advancement of clinical development.