Drive clinical innovation as a CRA II at ICON plc. Monitor trials for obesity and cardiovascular studies while fostering patient safety and data integrity.

In this key position, you will design, analyze, and monitor clinical trials at ICON. Collaborating with site staff and ensuring adherence to regulations is paramount as you contribute to the development of groundbreaking therapies. Your role insures high-quality clinical data and successful trials.

Key Responsibilities:
• Lead site qualification and initiation visits for trials
• Monitor compliance with protocols and patient safety
• Facilitate collaboration among investigators and site personnel
• Conduct data reviews to resolve queries promptly
• Assist in preparing clinical study documentation and reports

Requirements:
• Bachelor’s degree in a healthcare-related field
• At least 2 years of clinical trial monitoring experience
• Familiarity with...