Elevate your career in clinical research as a Clinical Research Associate II at Syneos Health, where compliance and monitoring take center stage. This position emphasizes remote and in office collaboration.
In the role of Clinical Research Associate II, you will be integral in monitoring clinical trials, executing site qualifications, and ensuring protocol adherence. You will work with cross-functional teams to maintain the integrity of trial data, react swiftly to issues, and optimize site processes. This position also involves recruitment and retention strategies, demanding excellent communication and organizational skills.
Key Responsibilities:
• Conduct site initiation, monitoring, and close-out visits
• Assess clinical data and resolve queries in a timely manner




• Maintain compliance with regulatory requirements and site documentation
• Document communications and activities according to SOPs
• Train and support site personnel for audit readiness
Requirements:
• Bachelor's degree or equivalent education/experience
• At least 12 months of relevant monitoring experience
• Familiarity with ICH/GCP Guidelines
• Proficient in computer skills and new technologies
• Willingness to manage frequent travel
Bring your expertise in site management and monitoring to Syneos Health and enhance clinical outcomes.
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📌 Experienced Clinical Research Associate II Role (Toronto)
🏢 Syneos Health
📍 Toronto