Found Description
Become a Site Management Associate in a hybrid role based in Mississauga, ON, with a company dedicated to improving lives through clinical research. This position centers on overseeing site operations, securing compliance, and facilitating information exchanges.
You will be responsible for managing supply logistics, ensuring regulatory processes, and maintaining key documentation. Ideal candidates have at least 2 years of clinical research experience, strong organizational skills, and familiarity with administrative tasks. Your contributions are vital in supporting clinical trial management and site coordination.
Key Responsibilities:
• Ensure the distribution and reconciliation of clinical supplies
• Handle regulatory and ethical submission processes
• Organize and maintain internal meeting agendas and documentation
• Provide training on study supplies and systems to site staff
• Manage documentation tracking for compliance and audits
Requirements:
• Degree ...
You will be responsible for managing supply logistics, ensuring regulatory processes, and maintaining key documentation. Ideal candidates have at least 2 years of clinical research experience, strong organizational skills, and familiarity with administrative tasks. Your contributions are vital in supporting clinical trial management and site coordination.
Key Responsibilities:
• Ensure the distribution and reconciliation of clinical supplies
• Handle regulatory and ethical submission processes
• Organize and maintain internal meeting agendas and documentation
• Provide training on study supplies and systems to site staff
• Manage documentation tracking for compliance and audits
Requirements:
• Degree ...
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