精鼎医药PAREXEL高薪诚聘CRA\统计师\DM leader\PM

新增职位ROA，相当于CRA助理，一年以上助理经验，本科或专科，英语读写能力尚可者可以投递简历。

回复 drfox 的帖子

社区医院的工作经历，行吗？

大哥，我现在的水平还不够，但立志能成为生物统计师。能指导下SAS吗？发个视屏教学可以吗？我的邮箱sanshao1604@163.com

回复 platypus 的帖子

; c6 o4 k8 T% N愿意考虑从ROA（研究助理)做起吗?以后可以转做CRA。

lipeilin8826 发表于 2011-3-23 14:24

                               
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$ c, H8 P/ q, Q! K0 k6 Z大哥，我现在的水平还不够，但立志能成为生物统计师。能指导下SAS吗？发个视屏教学可以吗？我的邮箱

( u, w% ]" E* ^5 Y8 T% _0 K3 J您好，我只负责招聘，不负责培训，谢谢！

有网友问是否找兼职的，不好意思，目前没有招聘兼职人员的计划。

招聘持续中，请符合要求的朋友继续投递简历。

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暂不招应届生，请勿投简历。
符合以下条件者投简历必复，谢谢！
合同制CRA\高级CRA
·      Bachelor / Master in life science/Nursing/ Pharmacy/Medical Sciences

·      At least 2 years’ work experience in clinical operations, particularly study monitoring.

·      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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. Q2 W) A/ Q; N* A! X1 jPM\PL\COL
·      Bachelor / Master in a science related field, with an advanced degree desirable
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·      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.

# _& \, u7 j2 l: m$ w/ p·      Critical Thinking & Problem Solving

·      Financial Management skills
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·      Strategic Thinking skills

·      Conflict Management skills

, u# j; m5 z" x. H, ^# [·      Consulting skills
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  q& Z% U2 p/ @" F. Y5 H6 G·      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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6 f0 W8 \" A$ B·         Provide medical monitoring for assigned projects and review all documents assigned for scientifically/medically relevant issues including drug safety.

·         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

! `$ G; ]8 }5 o$ o1 Y, ~·         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.

% C$ m0 b, i8 `) H3 v( k·         Excellent knowledge of drug safety and the drug development process

9 q- V6 Q& q, X5 r5 O·         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

7 w, D6 w4 |5 A8 u" D2 c·         Clinical practice experience

* O( b6 j5 ~: M  W·         Fluent English


RA注册事务专员 ·         Support Manager for all project and administrative works
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5 w% f' f* w9 l/ [4 k·         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

0 e8 E, [$ L0 p·         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

* p0 s# i5 ^, _  y) @$ j* d  _' c最新职位CRC，护理/医药专业，有一定英文读写能力，口语不要求，能够阅读英文方案，填写英文CRF即可，一年半，税后月薪3K以上，有意者请将简历发送者catherine.gan@lemonconsult.com.

目前比较急的职位是合同制CRA，注册事务专员RA，COL（Clinical operation leader）, DOL(Data management operation leader), Global project Leader,有意者请发送简历至catherine.gan@lemonconsult.com