上海相关职位: 质量专员/QC质检员 销售 IT工程师 (Helpdesk) 质谱分析助理研究员/副研究员 动物技术员 高级生物研发工程师 Technical Sales - OEM 药师 注册经理 项目管理部-高级研究员
周边城市招聘: 上海 浙江 安徽 广东 山东 河北 重庆 北京 江苏 湖南
企业入驻日期: 2017-11-09
职位描述: Position PurposeProvides managerial oversight of both colleagues and deliverables Performs duties of Clinical Programmer as needed Responsible for consistent harmonized processes and high quality clinical trial data for clinical projects in partnership with the Programming TA Lead Provides leadership of strategies for the implementation of technology-enabled processes Works closely with the Programming TA Lead in formulating strategies and standards to be implemented for all programs and takes responsibility for implementation.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 ManagedTeam consists of up to 8 Pfizer Colleagues and contractors (this may vary depending upon workload requirements)Primary Duties:Manages team of Clinical Programmers to deliver clinical programming services in a high quality and timely manner, and within CPW metrics goalsEnsures all clinical programming activities under remit conform to applicable standards, such as CDISC or PDS, and are in compliance with relevant regulatory requirementsAccountable for the implementation of clinical programming activities for studies and submissions related to the drug programs Ensures appropriate resources are identified and engaged to support the project workActively oversees Planisware project milestones and manages inconsistencies through networking with relevant CPMsProvides administrative and clinical programming technical and process oversight of teamAccountable 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 Performs Clinical Programmer activities as neededManages risk appropriately to enable innovative solutions which maintain timely, quality deliverablesManages use of resources in line with short, medium and long-term goalsImplements organizational design and develops succession planning for own group and for functional area under guidance of Programming TA LeadActively develops people under guidance of Programming TA Lead:Recruits high caliber staffProvides focused career development Provides performance managementManages retentionTraining & Education Preferred:Minimum of a B.S. Degree in either a Scientific or Business related field; Master Degree preferredBackground in Clinical Programming strongly preferredPrior Experience Preferred:At least 6 years of relevant industry experienceStatistical programming and clinical trials expertise with a thorough 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.).Strong communication (written and oral), leadership, decision-making, influencing, negotiation, and project management skills.Demonstrated experience managing projects and developing successful partnerships within study or asset teams.Demonstrated people management skills including recruiting and developing talent Proven ability to effectively operate in ambiguous situations.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 customersExperience 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
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。
研发实习生 120元/天
化验员 3-6千/月
分子生物实验员(上海) 4-6千/月
区域销售经理(广东省) 0.8-1万/月
助理分析员 3.5-6千/月
工艺分析员/质量研究员 6-9千/月
分析员/质量研究员 6-9千/月
助理研究员 4-6千/月
有机合成助理/研究员(应届生) 4-7千/月
项目专员 6-8千/月
助理分析员 3.5-6千/月
上海相关职位: 质量专员/QC质检员 销售 IT工程师 (Helpdesk) 质谱分析助理研究员/副研究员 动物技术员 高级生物研发工程师 Technical Sales - OEM 药师 注册经理 项目管理部-高级研究员
周边城市招聘: 上海 浙江 安徽 广东 山东 河北 重庆 北京 江苏 湖南
企业入驻日期: 2017-11-09