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 recent heights by joining Syneos Health as a Clinical Research Associate II.

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