精鼎医药PAREXEL高薪诚聘CRA\统计师\DM leader\PM

drfox · 发表于 2011-3-17 13:44:34

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。

platypus · 发表于 2011-3-23 13:24:47

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社区医院的工作经历，行吗？

lipeilin8826 · 发表于 2011-3-23 14:24:26

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

drfox · 发表于 2011-3-23 20:51:25

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愿意考虑从ROA（研究助理)做起吗?以后可以转做CRA。

drfox · 发表于 2011-3-23 20:54:40

lipeilin8826 发表于 2011-3-23 14:24

$ O% {% e# p7 {0 }- ]( F
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- `- d0 t: m$ T+ _# ]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

您好，我只负责招聘，不负责培训，谢谢！

drfox · 发表于 2011-3-31 21:48:20

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。

drfox · 发表于 2011-4-7 09:48:37

招聘持续中，请符合要求的朋友继续投递简历。

drfox · 发表于 2011-4-13 16:30:03

本帖最后由 drfox 于 2011-5-18 16:08 编辑

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.

PM\PL\COL
·    Bachelor / Master in a science related field, with an advanced degree desirable

·    PMP or equivalent desirable

·    At least 8 years and above proven relevant experience in healthcare, clinical research, project management or contract research organization.

·    Critical Thinking & Problem Solving

·    Financial Management skills

·    Strategic Thinking skills

·    Conflict Management skills

·    Consulting skills

·    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.

·    Owns the client relationship and responsible for client communication ensuring high client satisfaction.  Pro-active approach to providing solution set for clients

MA医学事务
·       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

·       Provide advice and support for feasibility studies and provide support for DMC and CEC management

·       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.

·       Excellent knowledge of drug safety and the drug development process

·       Medically qualified in an acknowledged Medical School with completion of at least a basic training in clinical medicine (residency, internship etc.)

·       Experience in Pharmaceutical Medicine desirable but not (initially) essential

·       Clinical practice experience

·       Fluent English

RA注册事务专员 ·       Support Manager for all project and administrative works

·       Management of certain projects for regulatory and IRB-related affairs.

·       A bachelor (or above) degree in life sciences or pharmaceutical background or equivalent

·       Minimum two years’ experience in Regulatory Affairs

符合要求者请发送简历至catherine.gan@lemonconsult.com

drfox · 发表于 2011-4-20 11:47:53

本帖最后由 drfox 于 2011-5-18 16:09 编辑

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.

drfox · 发表于 2011-4-27 12:22:09

本帖最后由 drfox 于 2011-5-18 16:09 编辑

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

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