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本帖最后由 drfox 于 2011-5-18 16:08 编辑
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% O6 \2 J3 A. K. [! d, D0 B暂不招应届生,请勿投简历。
9 a8 [" K* @4 p) V! J J3 J1 X8 X) I符合以下条件者投简历必复,谢谢!8 f1 M7 Y/ ^$ y6 \" h' Q, E
合同制CRA\高级CRA
: y4 @+ i$ r5 V$ F) m% B% [· Bachelor / Master in life science/Nursing/ Pharmacy/Medical Sciences
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2 d$ J6 f' V9 O7 `$ C# Z% q' ^9 s· At least 2 years’ work experience in clinical operations, particularly study monitoring.
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C3 j; h. e5 V- R$ S# ^0 W· Ability to speak and read the language(s) used locally in the country, plus a fluency in written and spoken English.
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· Bachelor / Master in a science related field, with an advanced degree desirable
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9 _; m$ _; `' v* _ @· PMP or equivalent desirable
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· At least 8 years and above proven relevant experience in healthcare, clinical research, project management or contract research organization. % b3 D; @9 Z/ a( f; d
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· Critical Thinking & Problem Solving
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0 [% P+ E3 I) t5 \" @· Financial Management skills
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0 T0 c4 q4 u9 y- Y5 u v+ Z· Strategic Thinking skills % I0 X' \) B! H* v6 R2 t+ J
. N! q9 J- h* o7 g. v! J$ z: ?/ C* D· Conflict Management skills
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· 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. ! v, K& b* X. [5 O7 E# @6 Y) _& A# A
; o4 [( \' X6 b# X- |· Owns the client relationship and responsible for client communication ensuring high client satisfaction. Pro-active approach to providing solution set for clients' L$ r3 h" h4 }' V
1 {6 [! ]2 h) P. F/ u8 JMA医学事务 w: D- I3 f2 q) |; j6 u8 Q
· Provide medical monitoring for assigned projects and review all documents assigned for scientifically/medically relevant issues including drug safety.+ E6 V% L1 r" H9 Q5 X8 [/ S
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· Function as medical representative/technical lead/senior technical lead on the projects, in Proposal Development Team and/or client meetings, z: C' ]3 D6 N' _% u) x( l
' z. ]4 ~, n& \+ t* d· 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.
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# m- n% x; _) D4 {% C+ U" [· Excellent knowledge of drug safety and the drug development process7 J1 Y* k7 T( e" K: |- [
5 S2 M2 ]6 g- n* Y' n9 y2 E& h· 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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( ?3 o9 Q, r8 C; d: F· Experience in Pharmaceutical Medicine desirable but not (initially) essential0 d) ?& ]+ \% O& z" @% I
2 g# X; [. V- Q/ I* l· Clinical practice experience & y- b) C2 U+ d$ B8 u5 m5 b
4 e2 f/ o# f) W s· Fluent English
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RA注册事务专员 · Support Manager for all project and administrative works7 \' E+ I5 e3 `+ N" S8 {
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· Management of certain projects for regulatory and IRB-related affairs.
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, h1 F" e( J' j# w· A bachelor (or above) degree in life sciences or pharmaceutical background or equivalent
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; h: Y( o1 |6 n1 e7 c3 K* j& r· Minimum two years’ experience in Regulatory Affairs C8 Z5 I+ R: t! Q9 {# Y: }
5 B; ?3 M+ G" |! y0 K$ V符合要求者请发送简历至catherine.gan@lemonconsult.com
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