As a retrospective analysis, a complete trial master document should be able to completely reproduce the process of clinical trials. The existence of test master document can prove the repeatability of data acquisition and has its scientific value.
Assist in the management of clinical trial documents and materials, cooperate with CRA (inspector) and project manager (project manager), and be responsible for the management and filing of TMF (clinical trial documents). Receive and follow up all research documents provided by CRA, assist in maintaining and updating TMF folders, regularly sort out TMF folder lists, and complete logistics work such as collection, printing, sending, scanning, archiving and management of clinical trial data.
Assist the project team to track the payment/reimbursement, contract and finance of clinical trial expenses. Track CRA's payment progress and invoice collection. Distribution management records of clinical trial substances. Other matters arranged by the project team.
TMF is a telecom management forum. Is a non-profit international trade association dedicated to improving business efficiency for service providers and other suppliers in the information industry, communication industry and entertainment industry.