Elevate your career as a Clinical Research Associate II with ICON plc, a leader in healthcare intelligence. Drive excellence in clinical trials by ensuring protocol compliance and patient safety across various sites.
This role requires a Bachelor's degree in a scientific or healthcare field and at least two years of Clinical Research Associate experience. You will conduct site visits, collaborate with investigators, and maintain high-quality clinical data while traveling extensively. Flexibility is key as you will work in both independent and collaborative settings to ensure smooth study operations.
Key Responsibilities:
• Conduct site qualification, initiation, monitoring, and close-out visits
• Ensure compliance with protocols and maintain data integrity
• Collaborate with investigators to facilitate study conduct
• Review data and resolve clinical data queries
• Prepare study documentation, including protocols and reports
Requirements:
• Bachelor's degree ...