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本帖最后由 drfox 于 2011-5-18 16:08 编辑
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! R9 q: |) l; Y6 r5 E暂不招应届生,请勿投简历。# O, V0 T* T/ |: v- P
符合以下条件者投简历必复,谢谢!
2 P6 D/ W+ l1 i8 _合同制CRA\高级CRA( S7 o! ?% r6 ?! E! W; C
· Bachelor / Master in life science/Nursing/ Pharmacy/Medical Sciences % V/ p1 [; h. S% l- H1 Y c4 o: ~1 `
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· At least 2 years’ work experience in clinical operations, particularly study monitoring. ( C" Q1 N1 S, {2 T+ G3 B$ k
7 s w- \6 a! A3 \· 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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9 C* ~* b# O8 p; ^, l; X5 ?· Bachelor / Master in a science related field, with an advanced degree desirable S6 l' t3 h4 b& o- _* L5 C1 B
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· PMP or equivalent desirable 4 z$ `) n0 L( x2 y* d
/ A$ V) {+ U @( A) X; b· At least 8 years and above proven relevant experience in healthcare, clinical research, project management or contract research organization. ; l3 y* v) l$ P
! o5 a6 M. X3 O6 F2 z3 r% b· Critical Thinking & Problem Solving
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· Financial Management skills
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· Strategic Thinking skills " d) G8 \4 i- X# m
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· Conflict Management skills
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- [/ c* g9 M1 r$ t· Consulting skills " O# I& A2 U7 V' j1 Q5 N& m( V
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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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8 c: ?1 N3 J+ J( f3 g' g) I7 k· Owns the client relationship and responsible for client communication ensuring high client satisfaction. Pro-active approach to providing solution set for clients% w! q, ^9 e" t: a" F& d* n
8 _8 g; o& l5 }) v Y0 J% b2 |) SMA医学事务
$ n" k6 q+ z7 `# h6 [· Provide medical monitoring for assigned projects and review all documents assigned for scientifically/medically relevant issues including drug safety.- C9 X' F' l5 d. l
! l* C; [: _* L! N) c8 \· Function as medical representative/technical lead/senior technical lead on the projects, in Proposal Development Team and/or client meetings
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. l* @9 P4 o0 z4 I( v: B% K. J· 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.: s' A- [5 x: e& K
* T4 O/ a: P/ }, M9 e· Excellent knowledge of drug safety and the drug development process
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K) S J* Z( K3 s· 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
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· Clinical practice experience
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· Fluent English
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* d. w) ~% o* \ U0 P; JRA注册事务专员 · Support Manager for all project and administrative works' D U; B2 ~+ t+ v
4 ` ?9 f {5 [' l" z( H7 w· Management of certain projects for regulatory and IRB-related affairs." v; s% A& y$ |" B7 [5 s4 H8 L8 s
+ d( z" a7 o+ I" a/ J* X· A bachelor (or above) degree in life sciences or pharmaceutical background or equivalent
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) s' j3 o# J! T& h8 B· 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( y; S0 U9 X+ e% R. G. \4 u O
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