诺华研发中心

【上海】诺华研发中心招聘实习生

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2009年3月18日 14:20  浏览:[26]

2006年11月, 作为其建立全球研发网络的重要一环, 诺华正式宣布将在上海张江高科技园建立一个综合研发中心. 该研发中心的建立体现了诺华一贯的承诺: 即通过对研发的整合加速对亚洲人群特异疾病的新药开发.
在全球4亿的乙肝病毒感染者中,大约三分之一在中国.此外据估每年中国大陆约有三十万人死于乙肝病毒导致的疾病. 研发中心现有的研发目标将主要着眼于传染性疾病导致的癌症, 如乙肝病毒导致的肝癌. 通过研究与发展实验室的共同努力与合作, 研发中心现已开展了几个新药研发项目的工作. 此外, 为满足本中心及全球的研发需求,中心也开始建立相应的疾病特异技术平台. 作为中心研发战略的重要部分,中心同时在积极寻求和本地区从事基础研究的科研院所合作的机会, 共同开发新技术和开展以作用机理为基础的新药研究.
2007年4月,诺华在浦东哈雷路的5000平方米的启动研发设施正式开始运转. 研发中心现有140位科研及辅助人员. 他们或来自本地科研院所, 生物科技和制药公司, 也有从西方国家归国的留学人员.该研发设施整合了化学,生物,分析及前期药物发展实验室并具备世界先进的实验仪器设备.
随着中心迅速增长的研发活动和人员需求, 诺华在张江高科技园中区建立的永久研发基地已在2008年破土动工. 该研发基地将拥有世界一流的研发设施, 集实用与优雅为一体并在设计中广泛体现"绿色环保"的概念. 第一期工程将覆盖38,000平方米的面积并由世界知名建筑师设计. 建成后将成为张江高科技园的地标之一.

Job ID	50662BR
Position Title	Intern for Clinical Trial Team
Work Location	Beijing China
Company/Legal Entity	China Novartis Institutes for BioMedical Research Co., Ltd
Functional Area	Translational Science
Job Type	Temp
Job Description	Assist in the operational and logistical aspects of clinical trials according to GCP (Good Clinical Practice) and relevant Novartis procedures and assist in delegated tasks to support the clinical trial team, ensuring that all essential documentation is collected, maintained and filed during the study. 1. Provide support to the Clinical Trial Leader (CTL) with many of the tasks involved with the smooth running of clinical trials in compliance with Novartis processes. Collaborate with the CTL in taking action to address issues as they arise. 2. Help manage clinical, regulatory and study-related essential documents such as study protocols, Case Report Forms, Informed Consent Forms etc.; review documents for completeness, accuracy and compliance with protocol and appropriate regulations. Identify issues and take appropriate corrective action as necessary. 3. Translate study documents from English to Chinese and Chinese to English. 4. Liaise with contract organisations, vendors and other suppliers of project support services to ensure study deliverables are met e.g. contribute to documentation, processes and set-up activities to facilitate efficient working and effective partnerships with external groups. 5. Provide input on agendas, create materials, liaise with meeting planners and coordinate logistics for key meetings e.g. internal CTL meetings or external investigator meetings. May attend and present at these meetings as appropriate. 6. Help ensure accuracy of clinical trial databases and resource tracking tools providing information and following up questions as necessary. Help check for discrepancies and take actions to correct as necessary. 7. Identify areas for process or technology improvements with regard to tasks undertaken within the role; propose and complete a project to enhance efficiencies and promote standardization across the organization based on this. 8. Assist in the forecasting, identification and ordering of clinical trial supplies. Recognize problems or delays and take action to prevent or address issues. Inform relevant project members as appropriate. 9. Responsible for setting up and maintaining Trial Master Files and ensuring all relevant study documents are filed and archived based on the appropriate guide-lines. 10. Attend Investigator/Site Initiation Meeting and First Dose/Monitoring Visit where required, and assist the CTL in organizing and conducting the meetings Keyword:CNIBR, NIBR Shanghai
Minimum requirements	1. A Bachelor's degree or in the final year of a Bachelor's degree program (for undergraduates), in life sciences. 2.Fluent English (oral and written) 3.Good organizational and interpersonal skills. 4.Attention to details. 5.Capable of clear written and verbal expression of ideas. 6.Ability to work independently and manage multiple priorities. 7.Computer literate. Good knowledge of Microsoft Office (Word, Excel, PowerPoint). 8.Some knowledge of clinical trial design, execution and operations would be beneficial.

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