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 Positive Clinical Practice and ICH guidelines
- Excellent computer and communication skills
- Must be prepared for up to 75% travel

Take your clinical research career to new heights by joining Syneos Health as a Clinical Research Associate II.

📌 Syneos Health Clinical Research Associate II Position (Toronto)
🏢 Syneos Health
📍 Toronto