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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。# b2 \4 n+ W5 t1 Q" E
符合以下条件者投简历必复，谢谢！
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· Bachelor / Master in life science/Nursing/ Pharmacy/Medical Sciences
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· At least 2 years’ work experience in clinical operations, particularly study monitoring. # x1 H, o" o; v) @
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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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· Bachelor / Master in a science related field, with an advanced degree desirable
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' O/ ^- e6 l& U3 y( P# l· PMP or equivalent desirable . J/ @2 [. Y8 e0 O
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· At least 8 years and above proven relevant experience in healthcare, clinical research, project management or contract research organization.
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4 c/ h4 z6 L$ q; L8 W% p* @- u· Critical Thinking & Problem Solving
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· Financial Management skills
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· Strategic Thinking skills 5 |. W) ~/ |- E$ x& P# Z
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· Conflict Management skills - {) u+ O4 R0 l+ D
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· Consulting skills . T- S4 U- ?4 H: q
: ^% d* e: s F· 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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- M9 m m9 K! D# C) x \+ M· 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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MA医学事务 : r6 R% e* E5 J2 U1 ?
· Provide medical monitoring for assigned projects and review all documents assigned for scientifically/medically relevant issues including drug safety.! Y4 m" I% J6 H' @0 }' W
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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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· Provide advice and support for feasibility studies and provide support for DMC and CEC management
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J: n+ ^+ D$ M5 x# P0 G· 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.)! k; ^2 J) ]9 |3 @1 D$ N0 ]5 H4 |4 w
% O+ ? K4 ^ H' ^' H" r· Experience in Pharmaceutical Medicine desirable but not (initially) essential0 W* S( W+ _( O+ p& V3 K. E( v
9 `9 _7 l+ o3 y# b/ W· Clinical practice experience
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; \9 G) |1 V+ r A· Fluent English' X; P% T5 ~4 o8 J
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6 m9 u& `% |4 J% M# h0 \* [RA注册事务专员 · Support Manager for all project and administrative works0 F) Q. y# ^- x2 K. }' M
+ G) L. Y2 u( v7 |. @6 w6 C8 g· Management of certain projects for regulatory and IRB-related affairs./ z4 W% F- \3 B# t# K
9 _% e# i( @/ s% c! N( J5 X· A bachelor (or above) degree in life sciences or pharmaceutical background or equivalent, _- t0 U# Z. Z7 b6 p9 J
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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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