Step into a pivotal role as a Site Management Associate I in hybrid settings in Mississauga, Ontario. Ensure effective site administration and communication in the dynamic field of clinical research.

You will manage daily interactions between clinical sites and vendors, oversee clinical supplies, and ensure compliance with regulatory requirements. This role is crucial for facilitating productive operations and supporting both internal teams and site staff. Training coordination, document management, and vendor-related tasks are essential functions of this position.

Key Responsibilities:
• Handle information exchange with various stakeholders
• Manage clinical supplies and inventory processes
• Coordinate ethical submissions and scheduled audits




• Facilitate internal and investigator meeting logistics
• Provide training on project-related systems

Requirements:
• At least 2 years of experience in clinical research
• Relevant college or university degree
• Understanding of Microsoft Office applications
• Fluency in English and French is essential
• Typing proficiency (minimum 40 WPM)

Bring your administrative skills and commitment to quality as a Site Management Associate I to support groundbreaking medical research.
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📌 Site Management Associate I for Clinical Research (Ontario)
🏢 PSI CRO
📍 Ontario