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本帖最后由 drfox 于 2011-5-18 16:08 编辑 7 T; u4 Q* k2 L# T6 \$ P# J& g% f& }
5 u" w( K9 |3 w+ } ?4 Q暂不招应届生，请勿投简历。
V& i' Y+ D4 ^- f- k' P符合以下条件者投简历必复，谢谢！) j) w! ^: n* Q9 F( G% ^2 I
合同制CRA\高级CRA+ W2 o- o2 O8 G! _5 C
· Bachelor / Master in life science/Nursing/ Pharmacy/Medical Sciences 8 G' O" f7 B0 M9 }- _% k7 s
/ M \% i2 A* D b; b+ q· At least 2 years’ work experience in clinical operations, particularly study monitoring.
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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.9 E1 L4 B% N+ _ f* [
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PM\PL\COL
% n- _( q2 W* b* S5 O5 C/ i· Bachelor / Master in a science related field, with an advanced degree desirable
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· PMP or equivalent desirable + L( U/ L) }# K/ N+ D' L; V# G
" O- }$ s6 N8 v' W8 v/ H· At least 8 years and above proven relevant experience in healthcare, clinical research, project management or contract research organization.
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· Critical Thinking & Problem Solving 5 Q( J# c6 W3 I1 A+ T0 _6 m2 G5 `
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· Financial Management skills
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2 b- _ V( ^9 b' w! G+ c& w· Strategic Thinking skills
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; ~' K! x+ p+ ^( P1 |2 r( f· Conflict Management skills
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· Consulting skills ' j& T7 l% Z) S
: p3 ~$ B: k8 S ?9 ^· 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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3 [( c+ F5 j# S0 \· Owns the client relationship and responsible for client communication ensuring high client satisfaction. Pro-active approach to providing solution set for clients
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5 g9 q5 ^: [' B1 h2 ?/ U* YMA医学事务
1 X) w' f: R7 \6 q· Provide medical monitoring for assigned projects and review all documents assigned for scientifically/medically relevant issues including drug safety. c, h1 V' m2 X0 a, h6 M
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· Function as medical representative/technical lead/senior technical lead on the projects, in Proposal Development Team and/or client meetings
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' s; q& c, U+ R# ~; |5 [7 Q; ~) ~; B2 X3 P· Provide advice and support for feasibility studies and provide support for DMC and CEC management
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) s4 _, D. ^& D4 E3 w· 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.
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% u/ J, v U5 P9 @$ r% A" L0 A· Excellent knowledge of drug safety and the drug development process
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5 f) j& [ P, ]& K6 k2 o· 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+ [$ c5 G* [ E+ S/ Y
5 j9 X: x- C' V6 {· Clinical practice experience
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`, ^. E8 p! C· Fluent English
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; D6 r; v0 u3 r- I8 u" vRA注册事务专员 · Support Manager for all project and administrative works' H0 Y% Y6 g, k" \( D
, s s& C, z# R. Y, ]4 r: ?· Management of certain projects for regulatory and IRB-related affairs.
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· A bachelor (or above) degree in life sciences or pharmaceutical background or equivalent
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· 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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