Job Description

ICON seeks a Clinical Research Associate II for the East Coast region to support sponsor-dedicated clinical trial operations. The role involves monitoring activities, ensuring protocol compliance, and maintaining data integrity across multiple study sites in a fast-paced environment.

Responsibilities

• Conduct site qualification, initiation, monitoring, and close-out visits
• Ensure protocol compliance, data integrity, and patient safety throughout trials
• Collaborate with investigators and site staff to facilitate study conduct
• Perform data review and resolve queries to maintain clinical data quality
• Contribute to preparation and review of study documentation 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, ICH-GCP guidelines, and regulations
• Strong organizational, communication, and attention to detail skills
• Ability to work independently and collaboratively in fast-paced settings
• Willingness to travel approximately 60% as required
• Legal right to work in assigned country

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