Clinical Research Associate II

Clinical Research Associate II role at ICON involving clinical trial monitoring, site management, and data integrity activities. The position requires a scientific bachelor's degree and minimum two years of CRA experience, with approximately 60% travel.

Responsibilities

• Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
• Ensure protocol compliance, data integrity, and patient safety throughout trial process
• Collaborate with investigators and site staff to facilitate smooth study conduct
• Perform data review and resolution of queries to maintain high-quality clinical data
• Contribute to preparation and review of study documentation including protocols and reports

Requirements

• Bachelor's degree in scientific or healthcare-related field
• Minimum 2 years of Clinical Research Associate experience
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
• Strong organizational and communication skills with attention to detail
• Ability to work independently and collaboratively in fast-paced environment
• Willingness to travel approximately 60% as required