Shape creative treatments as a Clinical Research Associate II at ICON Strategic Solutions in Vancouver. Contribute to vital clinical trial monitoring while utilizing your expertise in data integrity and protocol compliance.
ICON Strategic Solutions is offering a Clinical Research Associate II role dedicated to sponsor partnerships. Candidates should have at least two years of clinical trial monitoring experience and a bachelor's degree in a related field. You will be instrumental in maintaining patient safety and collaborating with site staff to ensure successful trial execution.
Key Responsibilities:
• Conduct site qualification, initiation, and monitoring visits
• Ensure compliance, data integrity, and patient safety




• Collaborate with investigators for effective study conduct
• Review data and resolve queries for accuracy
• Prepare and review essential study documentation
Requirements:
• Bachelor’s degree in a scientific or healthcare field
• Minimum 2 years of experience in clinical trials
• Knowledge of clinical trial regulations and ICH-GCP
• Strong organizational and communication skills
• Willingness to travel approximately 60%
Leverage your clinical research skills to advance healthcare and contribute to groundbreaking medical solutions at ICON.
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📌 Clinical Research Associate II Vancouver
🏢 ICON Clinical Research
📍 Vancouver