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本帖最后由 drfox 于 2011-5-18 16:08 编辑
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7 V u, Y% @# {& x, z; H暂不招应届生，请勿投简历。9 O% f p: m9 O9 _
符合以下条件者投简历必复，谢谢！
' \# b- @- _- h6 q& r5 r. {$ O合同制CRA\高级CRA/ {$ b) D" c2 W' F' ?, |" K8 L
· Bachelor / Master in life science/Nursing/ Pharmacy/Medical Sciences
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4 g. F: I: \; N% a7 e· 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.
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PM\PL\COL
1 l4 f% a, H& [· Bachelor / Master in a science related field, with an advanced degree desirable
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· PMP or equivalent desirable
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! N0 I6 C& b/ [% N/ E, |7 E9 |· 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
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· Financial Management skills
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, R, p! m$ x: `; U# z$ w# ?· Strategic Thinking skills - J7 Q: ?( y/ ^
5 `. O/ B: l2 ]% Y" K l· Conflict Management skills
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* f& L u5 J- U. A) O· Consulting skills
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' m: l: F# P0 z. _: Y$ f1 D· 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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· 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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- ^0 d V, \: O2 V) vMA医学事务
! S. S g# U: e. Y· Provide medical monitoring for assigned projects and review all documents assigned for scientifically/medically relevant issues including drug safety.
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$ t% [. n- m2 T3 Y· Function as medical representative/technical lead/senior technical lead on the projects, in Proposal Development Team and/or client meetings
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) @6 G' S5 b# m3 L1 [3 U· Provide advice and support for feasibility studies and provide support for DMC and CEC management
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$ D& a* C" q% s8 r1 y8 c) y/ q· 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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· Excellent knowledge of drug safety and the drug development process
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· 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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- n j$ i4 r: J& u· Experience in Pharmaceutical Medicine desirable but not (initially) essential
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4 D+ `% H$ p0 y9 {2 j· Clinical practice experience ! H/ }8 b* ?6 D$ D+ @0 f: q+ ]
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· Fluent English
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RA注册事务专员 · Support Manager for all project and administrative works) E0 C: O4 B0 Y
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· 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) E0 E+ `4 i* ?- m4 E1 d1 E
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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" N) g+ m/ {$ E4 O2 L$ J) F/ P
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