Clinical Trial Assistant (FSP) - Wuhan
Primary Location: China, Remote 求人ID R0000045293 Category Clinical Trials
About this Role
Key Role and Responsibilities Summary:
- TMF: Set up and maintain the site level TMF/cTMF, coordinate on document collection, uploading into SharePoint (SP)eTMF, check the document completeness, and provide TMF/eTMF quality control (QC) if required.
- EC Submission: Coordinate on EC submission dossier, site start-up preparation, and EC fee application and tracking.
- Process protocol amendments may include ICF updates.
- Tracker/Metrics Report: Collect and update study trackers/metrics report for site level if needed.
- Site Contract and Payment: Assist in contract signature process; assist in site level payment initiative and payment and invoice tracking.
- Site Materials and Equipment: Distribute site materials and equipment, document printing, shipment, and other administrative work.
- Administrative: Business and department office administration support if required.
- To undertake other reasonably related duties as may be assigned from time to time, as appropriate for level of experience
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