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 agile 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 effective 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.

📌 Site Management Associate I For Clinical Research Mississauga (Canada)
🏢 PSI CRO
📍 Canada