Clinical Trial Assistant Job in Toronto, Ontario Canada

Create and maintain company SOPs

Set-up and maintenance of the Trial Master File and tracking systems (sites, Regulatory Documents, Essential documents, Communication, Vendors, in accordance with project specifications).

Responsible for organizing and filing of all Central Files (TMF) as well as provide clerical support to the Clinical Research group as necessary.

Coordinate all aspect of communication and files related to the clinical trial in the TMF (Trial Master File)

Coordinate and conduct quality review of documents generated within the clinical team, or received from sites and monitors.

Ensure that all necessary documents and relevant study materials are available, maintained, tracked and files as applicable in the TMF

Responsibilities also include: