Advance your career as a Senior Clinical Research Associate in a energetic role focused on sponsor dedicated responsibilities. Manage clinical sites effectively through in office and remote monitoring.

As a Senior Clinical Research Associate, you'll oversee site compliance with Good Clinical Practice guidelines, ensuring that studies are conducted ethically and effectively. Your role will involve verifying patient consent processes, assessing site performance, and collaborating closely with project teams. Drive success in clinical research by delivering expertise in site communication and monitoring activities.

Key Responsibilities:
• Perform site management and monitoring tasks
• Ensure regulatory compliance throughout the study lifecycle




• Support patient safety and data integrity initiatives
• Oversee documentation and activity tracking
• Facilitate preparation for audits and site inspections

Requirements:
• Proven experience in clinical research and site monitoring
• In-depth knowledge of GCP and regulatory standards
• Solid problem-solving and analytical skills
• Excellent interpersonal and leadership abilities
• Ability to train and mentor junior staff

Utilize your skills to impact clinical research outcomes positively in this essential position.
J-18808-Ljbffr

📌 Senior Clinical Research Associate Role Ontario
🏢 Syneos Health
📍 Ontario