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本帖最后由 drfox 于 2011-5-18 16:08 编辑
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暂不招应届生，请勿投简历。/ w/ D+ J" T% l0 Q* I
符合以下条件者投简历必复，谢谢！4 f' x" c. {5 ^
合同制CRA\高级CRA$ t" L2 K' b- I& q4 Z
· Bachelor / Master in life science/Nursing/ Pharmacy/Medical Sciences ( l; {$ z* G9 D5 x# k
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· At least 2 years’ work experience in clinical operations, particularly study monitoring. ) t( ?4 F( Z9 H' k7 E0 ]5 M4 L5 i
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· Ability to speak and read the language(s) used locally in the country, plus a fluency in written and spoken English., G# T s0 p8 ?5 l
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· Bachelor / Master in a science related field, with an advanced degree desirable
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· PMP or equivalent desirable
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# E/ U) \- _" v4 O' j9 U! B: h· At least 8 years and above proven relevant experience in healthcare, clinical research, project management or contract research organization. / g# y' ]. g8 y( e. T
7 x7 f5 i6 S+ w& y$ d8 a- l· Critical Thinking & Problem Solving # E' |: r6 u9 \/ o! g$ w" s/ f
9 b: ?! \, C8 ]' B, W- r) J· Financial Management skills M* t4 U# B- _1 }" w/ K% m
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· Strategic Thinking skills
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$ a+ B; {, Q4 e, i/ o· Conflict Management skills
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6 Y. t: H( M6 z+ u! l4 j· Consulting skills
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· Late phase study phase experience necessary with large scale post-marketing, EAP and/or remote monitoring trials. Experience working with research-naive sites and in providing creative solutions to Sponsor organizations in the post-marketing area.
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+ [/ p* f I3 e7 N4 [0 q· Owns the client relationship and responsible for client communication ensuring high client satisfaction. Pro-active approach to providing solution set for clients* o1 F& Z5 n H1 n! R( b
' ]% H) V# X, c( qMA医学事务 & x8 _$ H; I3 {/ ?; w
· Provide medical monitoring for assigned projects and review all documents assigned for scientifically/medically relevant issues including drug safety.
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* `; w$ I( p2 x: t$ N( B· Function as medical representative/technical lead/senior technical lead on the projects, in Proposal Development Team and/or client meetings+ }6 v+ H8 ~3 A) L( Y" F$ @
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· Provide advice and support for feasibility studies and provide support for DMC and CEC management
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· Experience in clinical medicine (general or specialist qualifications) with a specialty in a “therapeutic area” which is expected to be kept up-to-date, the preference is cardiologist or internal medicine specialist with pharm experience.* T3 l- x( k M+ }$ X
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· Excellent knowledge of drug safety and the drug development process
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' J# \8 Y7 ^) E, c. E' C· Medically qualified in an acknowledged Medical School with completion of at least a basic training in clinical medicine (residency, internship etc.)
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· Experience in Pharmaceutical Medicine desirable but not (initially) essential x) l5 C/ B( ~9 o4 F1 z
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· Clinical practice experience
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· Fluent English
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RA注册事务专员 · Support Manager for all project and administrative works6 Z% m0 [% H, E7 f- ^% e5 P
$ z: W1 P- U9 ] W0 V: ?$ w· Management of certain projects for regulatory and IRB-related affairs.
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& ]* `4 m7 U/ W+ P· A bachelor (or above) degree in life sciences or pharmaceutical background or equivalent1 `7 y8 ~4 y1 g
2 [" Q. e6 R+ d" m8 T· Minimum two years’ experience in Regulatory Affairs
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符合要求者请发送简历至catherine.gan@lemonconsult.com
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