苏州招聘

Qualification/Experience 学历及经验要求

医药相关专业本科大二或大三学生
每周能保证3天以上出勤率
英语读写流利

Key Competencies 技能要求

? Excellent command of English, written and verbal, able to communicate effectively with stakeholders, managers and colleagues
精通英语口语和书写，充分具备与合作方，经理和同事有效沟通的技能
? Ability to carry out administrative and secretarial functions proficiently and in a timely manner.
熟练运用行政及秘书职能，按时完成工作要求
? Must be independent, pro-active, self-motivated with strong organizational, interpersonal and communication skills both written and verbal.
必须能够独立工作，积极主动，自我激励， 具备良好的组织及人际关系能力，及书面和口头沟通能力，
? Exhibited sound judgment to make decisions on sensitive issues as well as ability to work with confidential documents and information. Ability to act with tact and professionalism with all levels of management.
对于敏感问题能做合理恰当的决策；正确处理机密文件和信息的能力。具备以职业化形象和方式与各级管理层协同工作的技能
? Demonstrated resourcefulness with ability to anticipate needs, prioritize responsibilities, take initiative and work independently.
具备预见性，能够区分工作的优先顺序，主动独立的完成工作
? Flexibility and ability to work in a highly organized manner in an environment with frequent tight deadlines.
具备在紧迫的时间要求下，十分有条理并灵活工作的能力
? Demonstrated proficiency with all Pfizer software including Outlook, Word, Excel, PowerPoint, and XMS as well as internet applications with ability to learn new applications.
熟悉掌握所有工作所需的软件应用系统，包括办公室软件系统（Outlook, Word, Excel, PowerPoint, XMS），网络应用系统，并具备学习使用新的应用软件的能力
? Files all documents
具备文件归档能力
? Maintains department procedural documents
保存部门工作程序文件
? Assists staff with clerical duties such as faxing, photocopying, filing, document preparation, etc
协助同事的日常行政工作，如传真，复印，归档，文件准备等
? Orders and maintains department office supplies
订购并维护部门办公用品
? Schedules team meetings
安排小组会议时间
? Participates in appropriate training pertinent to performance
参加与职能相关的培训
? Responsible self-starter with attention to detail
高度负责，主动积极，关注细节
? Excellent follow-up skills
良好的工作跟进处理能力

On October 31, 2005, Pfizer announced the official opening of China Research and Development Center (CRDC) in Shanghai. Pfizer Global Research and Development’s Center is mainly engaged in drug development activities. Much of the facility's capacity is devoted to the study design, data management and statistical analysis of global phase I-IV clinical trials, as well as the clinical study report process. In addition, CRDC is a part of Pfizer global Safety and Risk Management and covers the functions of safety data processing and assessment. The center also trains Pfizer employees in China and throughout the Asia region in internationally recognized Good Clinical Practice standards.
辉瑞公司于2005年10月31日宣布辉瑞中国研发中心正式在上海揭幕。辉瑞中国研发中心主要为全球辉瑞药物开发提供支持工作。大部分的功能是围绕在I-IV期临床试验研究设计、数据管理和生物统计分析、以及临床试验报告的部分准备工作。此外，该中心是辉瑞全球安全和风险管理部的一个分支，负责安全数据处理和评估工作。研发中心还将为辉瑞公司在中国及亚洲的其它运营部门的员工提供国际标准的临床试验管理规范(GCP)的技术培训。