天津招聘

职位描述：
JD:
Responsibility:
1.Collect, translate, report, and follow up post-marketing non-serious AEs from all sources to Central team in timely manner;
2.Submit oversea Monthly Serious Adverse Drug Reaction Line Listings to SFDA in timely manner;
3.Distribute Safety Information, e.g. INDSR,PSRI and MSRI to study team onward to Investigators and ECs ;
4.Manage PV related documentations appropriately ;
5.Back up to other Safety Associate when required ;
6.Perform other PV related tasks when required.

Competence Profile:
1.医学、药学、生物相关学科的本科或以上学历，prefer更高；
3.良好的英文能力(必须)；
4.良好的沟通、协调及解决问题的能力。

If you are iterested in this position, pls send your resume to me : Apple.Tang@docsglobal.com 举报 分享

We are a global provider of consulting, and outsourced development and commercialisation services to pharmaceutical, biotechnology, medical device and government and public health organisations. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas. ICON has been recognised as one of the world’s leading Contract Research Organisations through a number of high-profile industry awards.