长沙招聘

Role Description
Position TitleDrug Safety Assistant -Case Book-In/Query Admin Associate
Division/OrganizationUs Drug Safety Unit
Line (i.e., Technology Infrastructure)Global Pharmacovigilance Office
Department (i.e., Application Hosting Services)Worldwide Safety & Regulatory Operations (WSRO)
LocationBridgewater/Collegeville/New York/Shanghai
Predicted Grade(s)Grade 6 (Technical)
Universal Role Set (optional)

Position Purpose

Execution of local activities relevant to the management of safety data

Primary Responsibilities
Monitor and manage dedicated DSU mailboxes
Maintain local documentation as required by legislation (including archiving/tracking/retrieval)
Support the submission and distribution of reports and relevant tracking
Support distribution and tracking of distribution of Follow-Up letters
Support inspection preparedness activities
Consistently apply Book-in & Data Entry policies and practices as per Company SOPs
Consistently apply Archiving policies as per Company SOP


Technical Skill Requirements
Demonstrated computer literacy, preferably in the use and management of relational databases
Ability, with supervision, to solve routine problems and to surface issues constructively
Ability to make basic decisions with an understanding of the consequences
Ability to achieve personal objectives while meeting departmental standards of performance
Ability to work under supervision in a matrix organization

Resources Managed (budget and FTEs)
N/A

Qualifications (i.e., preferred education, experience, attributes)
BSc in Life Sciences Preferred
High School Diploma Required
High attention to detail
High interpersonal skills
IT skills (Word / Excel)
Fluency in spoken and written English



Core Competencies (list 3-5 competencies only, see opportunities.pfizer.com for references
Functional/Technical Skills
Seizes Accountability
Grows Self
Change Agile
Self Awareness

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。