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JD:
1.Coordinate on EC submission dossier and site start up preparation;
2.Assist in prepare site materials and supply, document printing, shipment and contract signature and all the administrative work;
3.Setup and maintain the site level eTMF, coordinate on document uploading and remind the missing files with the CRA, provide eTMF QC if required;
4.Support CRA submit the study SUSAR/SAE by site or study requirements;
5.Assist in site level payment intiative and payment&invoice tracking.
Requirement:
1.CTA should have clinical trial related experience with the good potential and service awareness in the team;
2.Fluent in English (writing);
3.Excellent organizational skills and ability to prioritize and multi task;
4.Familiar with Microsoft word, Excel and PowerPoint.