-
3-4年经验 -
本科 -
招若干人 -
11-09 发布
- 五险一金
- 通讯补贴
- 专业培训
- 交通补贴
- 年终奖金
- 免费班车
职位描述
职位描述： Position Purpose1、Provides managerial oversight of both colleagues and deliverables 2、Performs duties of Clinical Programmer as needed 3、Responsible for consistent harmonized processes and high quality clinical trial data for clinical projects in partnership with the Programming TA Lead4、Creates, maintains and assumes accountability for a culture of high customer service using tools to facilitate communication, transparency of operations, clarity of workload balance, and alignmentResources Managed (budget and FTEs):Team consists of up to 5 Pfizer Colleagues and contractors (this may vary depending upon workload requirements)Primary Duties:1、Manages team of Clinical Programmers to deliver clinical programming services in a high quality and timely manner, and within CPW metrics goals2、Ensures all clinical programming activities under remit conform to applicable standards, such as CDISC or PDS, and are in compliance with relevant regulatory requirements3、Accountable for the implementation of clinical programming activities for studies and submissions related to the drug programs 4、Ensures appropriate resources are identified and engaged to support the project work5、Actively oversees Planisware project milestones and manages inconsistencies through networking with relevant CPMs6、Provides administrative and clinical programming technical and process oversight of team7、Accountable for timely reporting of relevant project metrics on quality, speed and compliance to Programming TA Lead and ensures timely cross-TA sharing for lesson learnt and accomplishment in CPW 8、Performs Clinical Programmer activities as needed9、Implements organizational design and develops succession planning for own group and for functional area under guidance of Programming TA Lead1、Actively develops people under guidance of Programming TA Lead:2、Recruits high caliber staff3、Provides focused career development 4、Provides performance management5、Manages retentionTraining & Education Preferred:1、Minimum of a B.S. Degree in either a Scientific or Business related field; Master Degree preferred2、Background in Clinical Programming strongly preferredPrior Experience Preferred:1、At least 3 years of relevant industry experience2、Statistical programming and clinical trials expertise with a basic understanding of the processes associated with clinical drug development and data analysis operations required for the reporting of clinical trial data (e.g. study reports, safety updates, global regulatory submissions, etc.).3、Solid communication (written and oral), leadership, decision-making, influencing, negotiation, and project management skills.4、Proven ability to effectively operate in ambiguous situations.5、History of achievement in a customer service role demonstrating ability to meet customer needs and address concerns and in building strong customer relationships, evidenced by positive feedback from customers6、Experience in leadership, project management, and resource management 职能类别： 生物工程/生物制药 临床数据分析员
联系方式
1
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。
