公司简介：

IQVIA是一家提供综合信息和技术解决方案的公司，致力于推动医疗健康行业的发展进程。世界各地的利益相关方均旨在通过创新治疗、患者照护和医疗可及性，来改善真实世界的患者结果。为了这一目标，利益相关方均与IQVIA合作，通过信息和技术服务解决方案，获得全新的行业见解和研究方法。IQVIA全球50000 人的团队凭借独到的见解、深入的商业和科学背景、精进的专业知识，助力客户提高临床、科研和商业成果，实现创新潜能，推动医疗健康行业长足进步。

​ Main Responsibilities:

•Assist Real-World study Project Manager to accurately update and maintain clinical systems that track site compliance and performance within project timelines. 

•Assist RWI team in the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. Assist with periodic review of study files for completeness.

•Assist RWI team with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.

•Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow. 

•Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.

•May perform assigned administrative tasks to support team members with team works execution.

•Partial assistant work for IQVIA RWI team, including assisting team meeting, training and all relevant activities.

Qualifications:

Bachelor degree in medicine, pharmacology, nursing, public health, biology or other life sciences; or equivalent combination of education, training and experience

Strong software and computer skills, including Microsoft Word, Excel and PowerPoint

Understand basic concept of clinical study

Minimum requirement for English is CET 6

[福利优势]：

1. 本科生12/h, 研究生15/h，超过800元的部分扣税

2. 茶水间饮料畅饮，零食小吃丰富

3. 世界500强公司，医疗健康咨询行业的佼佼者，大大增加你今后简历的含金量

 工作地址：  上海市静安区北京西路968号嘉地中心12楼