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Clinical Trial Assistant

The Programme

我们是目前中国生物医药企业中研发投入最多的企业

创造的力量、创新的科学氛围,以严谨逻辑解决问题的原则,跨学科团队协作,以及贯穿整个研发环节的对卓越品质的追求,是帮助我们实现所有成功的重要因素。

Responsibilities

  • Coordinate on EC submission dossier and site start up preparation
  • Assist in prepare site materials and supply, document printing, shipment and contract signature and all the administrative work
  • Setup and maintain the site level eTMF, coordinate on document uploading and remind the missing files with the CRA, provide eTMF QC if required
  • Support CRA submit the study SUSAR/SAE by site or study requirements
  • Assist in site level payment initiative and payment invoice tracking

Required Skills and Abilities

  • CTA should have clinical trial related experience with the good potential and service awareness in the team
  • Fluent in English (writing)
  • Excellent organizational skills and ability to prioritize and multitask
  • Familiar with Microsoft word, Excel and PowerPoint
Closed a year ago
Closed a year ago
  • Job type:Graduate Jobs
  • Citizenships:

  • Locations:

    Beijing (China)

  • Closing Date:21st Mar 2019, 6:00 pm

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