[北京]辉瑞公司招聘2012招聘实习生

1、医学信息实习生（北京），职位工作地点在北京，招聘人数1名。简历收集邮箱：talent.china@

工作描述:

基于公司内外部医学信息资源，为内外部客户提供医学信息检索服务，协助业务团队达成整体目标。

工作内容:

客户医学信息咨询

l          检索公司内外医学数据库，为内、外部客户提供非产品相关医学信息

l          为内部客户提供非产品相医学文献支持

l          支持医学信息团队日常工作

教育背景和工作技能要求:

教育背景

l          医学、药学或医学信息学本科或以上学历在校生

l          保证每周四个工作日或以上的实习

经验、技能

l          熟练使用医学文献数据库

l          熟练掌握Microsoft Word, PowerPoint and Excel

l          较好的英文会话及读写能力

l          良好的沟通能力

 

 

2、医学事务实习生（北京），职位工作地点在北京，招聘人数1名。简历收集邮箱：talent.china@

工作描述:

基于相关领域医学项目，给予项目执行的支持、文件准备和团队支持。

工作内容:

l        承担医学领域项目部分工作

l        支持competitive grant和IIR 状态更新和与外部客户非产品相关沟通工作

l        支持医学事务团队日常工作

教育背景和工作技能要求:

教育背景

l          临床医学或药学本科或以上学历在校生

l          保证每周三个工作日或以上的实习

经验、技能

l          熟练使用医学文献数据库

l          熟练掌握Microsoft Word, PowerPoint and Excel

l          较好的英文会话及读写能力

l          良好的沟通能力

 

3、药品注册运作实习生（北京），职位工作地点在北京，招聘人数1名。简历收集邮箱：talent.china@

MAIN REPONSIBILITIES / DUTIES

·           The position will manage activities that provide Regulatory Operational support for China product portfolio including pre-registration, registration and post approval activities to ensure WRS EM China team work efficiency and work delivery. This responsibility will be accomplished through assisting line manager to develop, implement and maintain sound regulatory team work system /work flow/procedure for all IND/NDA/CTA and in-line product maintenance related activities. The role may also be assigned to take lead on special project.

·           The role supports WRS EM China team by developing and overseeing local procedure and practices to ensure quality outcome that meet WRS EM China team objectives. The role is also responsible for ensuring full compliance to all local regulations and company SOPs, local IGs.

·           The role will work closely with Regulatory Effectiveness manager.

·           Work closely with TA registration team in providing effective operational support for entire product registration lifecycle.

·           Implement and maintain work system for Registration master file management, Regulatory contact record management.

·           Implement registration archiving system for all types of registration dossier, approval documents, and ensure good maintenance 

·           Support REM to oversee the compliance by operating to the regulatory related system/database in accordance with SOP/IG requirements and conducting regular quality reviews for regulatory related system/documentations for GDMS/GRS/PfLICC/RT-II CTA

·           Support REM to liaise with TA registration team to develop/update  local SOP/IG pertaining to Regulatory aspects  as per the requirement  from corporate SOP if needed

·           Ensure tasks and projects are completed effectively and efficiently

 

REQUIRED SKILL SET

·         Technical

Strong Customer focus sense

Excellent communication & interpersonal skills

Excellent Teamwork/collaboration

Result orientated

Quality orientation

Excellent ability to research information

Able to work under pressure in a busy environment

Good working knowledge of Microsoft Word, PowerPoint and Excel

Excellent English skill in speaking, reading and writing

·         Education

2012 or 2013 graduates or post-graduate

Bachelor degree or above, Qualifications in healthcare, pharmaceutical is preferred.

Able to work at least 3 days a week

 

 

公司介绍

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