Associate Manager, Regional Regulatory Affairs
科文斯医药研发（北京）有限公司上海分公司
- 公司规模：500-1000人
- 公司性质：外资(欧美)
- 公司行业：制药/生物工程
职位信息
- 发布日期：2013-10-14
- 工作地点：北京
- 招聘人数：若干
- 工作经验：五年以上
- 学历要求：本科
- 语言要求：英语精通
普通话精通 - 职位类别：药品注册
职位描述
About the Job:
* Provide consultation to the Regulatory Strategy Regional team
* Provide consultation to China Regulatory submission team
* Update all regulatory related policy to the RA team.
* Research relevant information to support registration projects.
* Prepare and coordinate the document preparation of submissions if needed.
* Prepare and coordinate samples export application if needed.
* Any duties are requested by regulatory management.
Requirements:
* At least five years regulatory affairs working experiences in Pharmaceutical/CRO Industry.
* A Bachelor degree or above of medical, pharmacy and relevant majors
* Good relationship with the relevant authorities.
* Good communication skills both in Chinese and English.
About Covance:
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Covance Clinical Development Services is based on an integrated clinical development services that is unique to Covance as we are one of the few truly global drug development companies positioned to provide comprehensive clinical support from First-in-Human studies through pivotal Phase III global clinical trial
At Covance, you'll discover your professional home to learn, grow and achieve. We offer careers with a purpose in an environment that values achievement, supports a balance between your personal and professional life, and allows you to make meaningful contributions to human healthcare.
Why Covance?
At Covance, you can make a difference by helping to deliver life-saving and life-enhancing medicines to people around the world. Our commitment to this mission has resulted in Covance’s impressive history of company stability and growth. We’ve achieved these results by fostering a work environment that encourages, develops and leverages our team’s capabilities. Covance’s ongoing success offers team members unsurpassed growth and career development opportunities. There’s no better time to join us!
* Provide consultation to the Regulatory Strategy Regional team
* Provide consultation to China Regulatory submission team
* Update all regulatory related policy to the RA team.
* Research relevant information to support registration projects.
* Prepare and coordinate the document preparation of submissions if needed.
* Prepare and coordinate samples export application if needed.
* Any duties are requested by regulatory management.
Requirements:
* At least five years regulatory affairs working experiences in Pharmaceutical/CRO Industry.
* A Bachelor degree or above of medical, pharmacy and relevant majors
* Good relationship with the relevant authorities.
* Good communication skills both in Chinese and English.
About Covance:
<!--[if !supportLineBreakNewLine]-->
<!--[endif]-->
Covance Clinical Development Services is based on an integrated clinical development services that is unique to Covance as we are one of the few truly global drug development companies positioned to provide comprehensive clinical support from First-in-Human studies through pivotal Phase III global clinical trial
At Covance, you'll discover your professional home to learn, grow and achieve. We offer careers with a purpose in an environment that values achievement, supports a balance between your personal and professional life, and allows you to make meaningful contributions to human healthcare.
Why Covance?
At Covance, you can make a difference by helping to deliver life-saving and life-enhancing medicines to people around the world. Our commitment to this mission has resulted in Covance’s impressive history of company stability and growth. We’ve achieved these results by fostering a work environment that encourages, develops and leverages our team’s capabilities. Covance’s ongoing success offers team members unsurpassed growth and career development opportunities. There’s no better time to join us!
公司介绍
Covance is one of the world’s largest and most comprehensive drug development services companies with more than 10,000 employees in 60 countries. Through its nonclinical, clinical and commercialization services, Covance has helped pharmaceutical and biotech companies develop one-third of all prescription medicines in the market today.
Well come to our online job pool to dig out more opportunities at:
http://careers.covance.cn/
Well come to our online job pool to dig out more opportunities at:
http://careers.covance.cn/
联系方式
- 公司网站：http://www.covance.com
- Email：calvin.xu@covance.com
- 公司地址：上海市黄埔区西藏中路268号来福士广场1806室
- 邮政编码：200001
- 联系人：Vicky Qu