美资医药公司急招监察员

http://www.druggcp.net/bbs/viewthforum.php?mod=viewthread&tid19279&extra=page%3D1
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# }9 d  P+ ^8 b$ C1 ~- X5 u* A& gCRA:
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- S# p, ]* J8 IRequirements::
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3 U# A! O" f4 I( o1 d0 W; |At least 8 months working experience as CRA/monitor, or have managed at least 2 clinical trials as monitor;
1 r* p2 W; I3 G  VMajor in clinical medicine, bachelor’s degree or above;
Good English skill with CET-6 certificate or TOFEL/GRE achievement;
Good communication skill and team spirit; good computer skill.
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Responsibilities:
# b# X( I1 d# W7 F- ]As main connection with investigators, to monitor clinical study from site selection to on site monitoring, to make sure clinical trial is conducted in compliance with ICHGCP, with the requirements of Regulation and sponsor.
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/ |3 [3 o$ u+ K$ j' w# nExcellent candidates may have chances to be recommended to multinational pharmaceutical companies to obtain enough training.


/ t8 x/ a$ g" C  I% A- ^有意者请发简历至一下邮箱：lxh542@yahoo.com.cn

本科药剂,硕士医药管理,请问是否还需要招人?