Clinical Trial Assistant
TransPerfect
Oct 2016 - Sep 2017 (1 year)
• Establish and maintain the tracking tools for assigned trials.
• Create, assemble and coordinate shipping of study materials.
• Conduct initial review and tracking of invoices & study payments.
• Receive clinical study documents from study team, review for completion, accuracy & expiration, and submit to the TMF.
• Generate, review & approve TMF document workflows.
• Review TMF inventory for missing and expiring documents.
• Support Clinical Document Control Specialist, LCRA and CPM to track and file documents and study metrics.
• Support maintenance of the Trial Master File (TMF) and assist in quality control as appropriate.
• Review and assist in the collection of essential documents for completeness and compliance with SOPs, the protoc