长沙招聘

职位描述：
Role Summary:
? Responsible for ensuring efficient and effective administrative operations within Clinical Trial Management(CTM)
? To administrate duties, the Assistant may also be assigned to coordinate special projects or tasks and will contribute to the achievement of CRDC or relevant center-wide objectives

Responsibilities:
? Provides support in administrative duties including, correspondence, facility and stationary support, phone coverage, colleagues on boarding/off boarding, calendar management, scheduling and logistics of meetings, travel arrangement, expense reports, contact list update, etc.
? Provides administrative support for team colleagues according to established procedures (e.g., GCE, Ariba, travel authorization, etc.)
? Provides administrative support for team colleagues on inspection readiness compliance including CV compliance, P2L training on time completion, etc.
? Provides support to visitors from other facilities in areas related to travel, local transportation, and logistics
? Populate paper work in preferred format with provided information and support preparation of tracking log, reports, and presentations
? Interacts with colleagues in a constructive, professional way to process requests and deliver expected level of service

Qualifications (Training, Education & Prior Experience):
? Bachelor's Degree preferred
? Demonstrated proficiency with commonly used office software including Outlook, Word, Excel, PowerPoint, and XMS as well as internet applications with ability to learn new applications
? Uses e-mail, face-to-face and telephone contacts appropriately
? Builds good working relationships with all colleagues 举报 分享

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。