Clinical trial monitoring and data review define this Clinical Research Associate II position at ICON Strategic Solutions, with approximately 60% travel required. Support sponsor-dedicated studies while protecting protocol compliance and patient safety.
At ICON, a Clinical Research Associate II contributes to clinical trial monitoring activities and takes responsibility for assigned deliverables. You will conduct site visits, collaborate with investigators, review clinical data, and support study documentation. The position requires clinical trial monitoring experience and knowledge of ICH-GCP guidelines.
Key Responsibilities: Conduct site qualification, initiation, monitoring, and close-out visits
Ensure protocol compliance, data integrity, and patient safety




Collaborate with investigators and site staff
Review data and resolve queries
Prepare and review protocols and clinical study reports
Requirements: Bachelor's degree in science or healthcare
Minimum two years as a Clinical Research Associate
Knowledge of clinical trial processes, regulations, and ICH-GCP
Solid organization, communication, and attention to detail
Willingness to travel approximately 60%
Bring clinical monitoring, data review, and regulatory knowledge to sponsor-dedicated trials supporting high-quality studies at ICON Strategic Solutions.

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📌 Clinical Research Associate II (Newfoundland and Labrador)
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📍 Newfoundland and Labrador