上海相关职位: 生物信息工程师 MSL 医药销售代表 肿瘤生物研究员技术人员 药物与包材分析方法研发经理/技术负责人/实验室经理 CRA 区域主管/经理 (肿瘤方向) GLP/GMP工程师/质量体系工程师 品管助理 临床项目经理 医疗耗材销售代表
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: Responsibility:General Management:1)People development for direct reports, perform performance review with direct reports, discuss and approve development plan for direct reports;2)Overview project management quality and process for direct reports; Support direct reports on project management and site management;3)Review clinical research SOP and provide input on SOP revision;4)Provide training and guidance to junior team members and business partners;Project Management:1)Set up and lead the project team to ensure the study is implement according to company policy, SOP and relative regulations.2)Lead the project team to accomplish the proposed timeline;3)Communicate with internal and external customers in terms of project progress and outstanding issues;4)Lead the protocol design and approval process, provide scientific and feasibility input on the protocol and other study documents design;5)Evaluate the potential investigational sites for a specific study in terms of the quality of the investigator and the suitability of the sites;6)Prepare study budget proposal based on fair market value. Ensure the study is operated according to the budget.7)Actively guide and coach CRAs in the study team;8)Coordinate with data management, statistician and medical writer to generate the statistical report and study report;9)Evaluate the CRO, provide evaluation assessment to line manager;10)Perform co-monitoring to team members.Monitoring:1)Initiate, monitor and close up clinical studies in compliance with study protocols and company’s guidance, on budget, and on time plan;2)Document and archive all clinical trial relevant activities;3)Verify the accuracy, completeness and legibility of the data collected in the studies;4)Ensure all case report forms be collected, queries be transferred between the company and the investigators in a timely manner;5)Endure all adverse events occurred in the study be reported in compliance with study requirements;6)Verify the trial supply to be transferred, stored and prescribed appropriately, and unused drugs to be returned or destroyed properlyTechnical / Professional Knowledge Input:1)Provide feasibility assessment and input at project planning stage based on a satisfactory level of technical and professional skill or knowledge in position related areas;2)Provide input on training curriculum based on current developments and trends in areas of expertise;3)Provide local insight on global clinical trialsRelationship Building:1)Build up and maintain healthy relationships with internal and external customers via smooth and efficient communications through the clinical studies;2)Support the direct report to build up and maintain good relationships with study sites and internal customers.Vendor Management:1)Perform vendor selection and continuous quality and compliance tracking and evaluation2)Perform effective and efficient vendor management to ensure the services vendor provided are satisfied and qualified in compliance with J&J policy, SOP and other related requirements.Other responsibilities defined in written procedures.Personal Requirements (include experience, knowledge, skills and education)-Bachelor degree & above, clinical medicine would be preferred-At least 5 years’ experience in clinical research execution, include at least 2 years project management experience-Strong people communication skill-Good project management skill ( e.g. good planning, implementation and follow up) is required-Fluent in English speaking, reading and writing-Good presentation skill-Good people management skill 职能类别: 临床研究员
虹桥路355号城开国际大厦
美国强生公司是世界上最大的、综合性的医药保健公司之一,也是世界上产品最多元化的公司之一。公司成立于1886年,迄今为止已在世界54个国家设有197家分公司,产品畅销全球所有国家和地区。强生公司为世界500强企业,长期以来,强生公司在各个领域获得一系列殊荣:自1986年起,强生公司被《职业母亲》杂志连年评为职业母亲的***公司。2002年被《财富》杂志评为全美最受推崇的10佳企业;被《商业周刊》评为2001年度全美***经营业绩的上市公司,2002年度全美50家表现最杰出公司榜首; 强生(中国)医疗器材有限公司系美国强生公司在中国的独资企业,从事高质量的医疗器械的生产和经营。 在翰威特公司与《哈佛商业评论中文版》联合进行的2009年亚洲***雇主调研中,强生(中国)医疗器材有限公司位列“2009年中国十佳雇主”。 因业务扩展的需要,招聘职位,在所述地点工作: 工作报酬:公司将提供有竞争力的工资及奖金,各项社保及强生公司的完善福利待遇。 为保证简历的有效性和及时性,请按照系统流程投递;但考虑到人员系统硬件的水平不同,我们也接受邮件简历 公司将在2周内通知第一批面试者。公司将对所有应聘者的个人资料予以保密。 欲查询更多强生中国医疗招聘信息,请登陆www.careers.jnj.com
原核工艺开发主管 1-1.5万/月
临床研究监查员(CRA) 1-1.5万/月
风湿-区域市场经理 0.8-1万/月
安装经理 0.7-1.1万/月
上海松华药业中心实验室QC员 4.5-6千/月
生物信息总监 25-30万/年
市场销售(检验领域) 4.5-6千/月
口腔医疗器械销售代表 5-8千/月
产品经理 1-1.2万/月
分销代表-河南 4.5-6千/月
分销代表-河南 4.5-6千/月
分销代表-两湖 4.5-6千/月
上海相关职位: 生物信息工程师 MSL 医药销售代表 肿瘤生物研究员技术人员 药物与包材分析方法研发经理/技术负责人/实验室经理 CRA 区域主管/经理 (肿瘤方向) GLP/GMP工程师/质量体系工程师 品管助理 临床项目经理 医疗耗材销售代表
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