-
1年经验 -
本科 -
招1人 -
11-09 发布
职位描述
职位描述： Role Description * Ensure staff/team alignment to agreed global Dev Ops strategic direction. * Provide day-to-day management of the activities supporting both data management (DM) and technical operations (Tech Ops). * Promote the use of consistent, efficient, and quality processes to meet timelines and deliverables for the site based project teams. * Maintains close contact with key collaborators and peer leaders within CDS to understand their expectations and perceptions. * Ensures implementation of effective systems, policies and procedures in support of CDS functions.* Collaborate with peer leads in CDS to develop and maintain a support model tracking system and to facilitate issue resolution and capture corrective actions. * Provide for appropriate metrics generation and reporting.* Create, maintain and assume accountability for a culture of high customer service and continuous process improvement using tools to facilitate communication, transparency of operations, clarity of workload, and alignment on priorities.* Motivate and inspire staff in order to lead them through difficult situations Qualifications Previous experience of leading a clinical data management group, or responsibility for a substantial clinical data technical function, or equivalent* Thorough understanding of business area and applicability within large, matrix organization* Demonstrated experience managing a team of direct reports* Demonstrated ability to thoroughly assess complex situations and implement appropriate solutions through effective decision making* Ability to creatively address issues and situations in support of global, outsourced environment.* Proven negotiation and influencing abilities* Sustained focus on successful project delivery while driving and supporting relevant innovation initiatives concurrently* Record of sustained high customer service/focus* Experience interacting with virtual/remote customers and/or project teams* Ability to design and capture appropriate performance metrics required for oversight* Extensive knowledge of vendor processes, contracting, and best practices in outsourcing* Capable of building strong relationships with application and service providers 职能类别： 生物/制药/医疗器械 临床数据分析员
联系方式
光谷生物城
公司信息
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。
