Join a leading team as a Clinical Research Associate focusing on site monitoring in a sponsor dedicated capacity. This versatile role allows for both remote and site-based work. In this position, you will ensure the integrity of clinical trials by conducting comprehensive site assessments, verifying consent processes, and maintaining compliance with applicable regulations.

You will be tasked with managing site-level activities, communicating effectively with investigators, and contributing to audit readiness. Your expertise in monitoring processes will play a critical role in the success of clinical projects. Key Responsibilities:
Conduct in office and remote monitoring visits
Verify accuracy of clinical data and site documentation




Manage inventory and compliance of investigational products
Document and communicate site performance issues
Participate in training and meeting preparations Requirements:
Experience in site monitoring and clinical research
Knowledge of GCP and regulatory compliance
Robust organizational and communication skills
Ability to adapt to evolving project demands
Mentorship experience is a plus Make a significant contribution to advancing clinical trials and ensuring quality in research activities.

📌 Clinical Research Associate – Monitoring Specialist Toronto
🏢 Syneos Health
📍 Toronto