Become a Clinical Research Associate II at Syneos Health and play a pivotal role in clinical trial success through site management and monitoring. This position allows for flexibility with both field and remote work.
As a key member of Syneos Health, the Clinical Research Associate II will oversee site compliance, conduct monitoring visits, and facilitate project workflows. Your role will require you to act on-site and remotely to ensure patient safety and regulatory compliance, addressing issues promptly. You will track recruitment efforts and maintain critical documentation while evolving with a supportive team.
Key Responsibilities:
• Execute site qualification and interim monitoring visits
• Ensure informed consent processes are properly followed




• Conduct thorough reviews of site documentation
• Facilitate communication among team members and sites
• Prepare for audits and maintain compliance
Requirements:
• Bachelor’s degree or RN in a relevant discipline
• 12 months of monitoring experience required
• Knowledge of Good Clinical Practice and ICH guidelines
• Excellent computer and communication skills
• Must be prepared for up to 75% travel
Take your clinical research career to current heights by joining Syneos Health as a Clinical Research Associate II.
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📌 Syneos Health Clinical Research Associate II Position (Toronto)
🏢 Syneos Health
📍 Toronto