Clinical Trial Assistant

• Manage clinical and non-clinical supply in collaboration with other country roles
• Collate, distribute/ship, and archive clinical documents
• Manage labeling requirements and coordinate/sign translation change requests
• Prepare documents and correspondence
• Ensure collection and distribution of study tools and documents
• Update clinical trial databases (CTMS) and trackers
• Assist with eTMF reconciliation
• Document proper destruction of clinical supplies
• Execute the eTMF Quality Control Plan

Explore Clinical Trial Assistant – Supply at Fortrea. Review requirements and application details.