Job Description
Advance your career with ICON plc as a Clinical Research Associate II, focusing on obesity and cardio studies. Monitor clinical trials, analyze medical data, and ensure patient safety throughout the process.
In this dedicated position, you will leverage your clinical trial monitoring skills to conduct site visits, ensuring protocol compliance and data integrity. Collaboration with investigators and site staff is key to facilitating smooth study conduct. Your analytical skills will contribute to the high-quality resolution of data queries and preparation of essential study documentation.
Key Responsibilities:
• Conduct site qualification, initiation, monitoring, and close-out visits
• Ensure compliance, data integrity, and patient safety
• Collaborate with investigators and site staff
• Perform data review and query resolution
• Contribute to protocols and clinical study report preparation
Requirements:
• Bachelor’s degree in a scientific or healthcare field
In this dedicated position, you will leverage your clinical trial monitoring skills to conduct site visits, ensuring protocol compliance and data integrity. Collaboration with investigators and site staff is key to facilitating smooth study conduct. Your analytical skills will contribute to the high-quality resolution of data queries and preparation of essential study documentation.
Key Responsibilities:
• Conduct site qualification, initiation, monitoring, and close-out visits
• Ensure compliance, data integrity, and patient safety
• Collaborate with investigators and site staff
• Perform data review and query resolution
• Contribute to protocols and clinical study report preparation
Requirements:
• Bachelor’s degree in a scientific or healthcare field
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