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本帖最后由 drfox 于 2011-5-18 16:08 编辑 # |6 Z3 j; I; ]4 }( D1 i
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暂不招应届生，请勿投简历。
: g g+ s+ q, o2 |6 u5 R, l& ~符合以下条件者投简历必复，谢谢！' C5 M3 Q9 D5 `7 q3 O0 G
合同制CRA\高级CRA
, h7 Q/ z: V, e: ?7 a· Bachelor / Master in life science/Nursing/ Pharmacy/Medical Sciences
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, n+ Y1 g) J2 P- G* }. V· At least 2 years’ work experience in clinical operations, particularly study monitoring.
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$ J) H3 r; O* {! ^, |· Ability to speak and read the language(s) used locally in the country, plus a fluency in written and spoken English., C% L2 Y0 Y$ T9 j7 o
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· Bachelor / Master in a science related field, with an advanced degree desirable
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. v: f9 q$ @9 M· PMP or equivalent desirable 6 s& I- ^, D8 b W7 k4 S8 W
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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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· Critical Thinking & Problem Solving
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% z. V. r. t7 A; y" @. K· Financial Management skills
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8 f( X, v/ O3 r) i" Q· Strategic Thinking skills
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! `5 _* R n' n/ u* l/ X· Conflict Management skills
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4 _: o6 `7 H# r1 \/ j· Consulting skills ; ~% L. I k$ K5 m8 q* a
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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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· 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
" V; @; B4 d$ `· Provide medical monitoring for assigned projects and review all documents assigned for scientifically/medically relevant issues including drug safety.
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· Function as medical representative/technical lead/senior technical lead on the projects, in Proposal Development Team and/or client meetings) ` F/ T. A4 ^
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· Provide advice and support for feasibility studies and provide support for DMC and CEC management! [' J1 f" h( _+ ^7 F
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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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. Y1 e# ?: `5 u7 z) N, d# B! J! U· Excellent knowledge of drug safety and the drug development process% N% D P* W7 W/ n9 r5 P7 q
- W0 D% u; _1 Y; N- F· 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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' P* I# r# a$ l# P" F8 A7 O· Experience in Pharmaceutical Medicine desirable but not (initially) essential1 K$ n) Q9 U/ B* {0 Z
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· Clinical practice experience & C7 \, H# T8 y, x4 T" B
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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$ N% _/ q6 h) c r5 f! o; W9 B
/ g- `- b' |2 }6 @' S9 K, w, X3 k· Management of certain projects for regulatory and IRB-related affairs.4 m' ~ d) Z" H0 O5 @3 V+ N: F* R
5 o4 Y2 t1 j n! U1 A· A bachelor (or above) degree in life sciences or pharmaceutical background or equivalent% }+ l$ X: [! ^" D" j
: E+ ^0 T/ o+ c8 j' f6 F0 b· Minimum two years’ experience in Regulatory Affairs
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8 D8 t( M( ?- f* X9 b+ w符合要求者请发送简历至catherine.gan@lemonconsult.com
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