• 3-4年经验
  • 博士
  • 招1人
  • 11-09 发布
  • 五险一金
  • 定期体检

职位描述

职位描述: Description:1.Design and execute nonclinical toxicology study protocols, analyze and interpret the results, and write a final report of the findings;2.Monitor all aspects of a study during the In Life phase;3.Assure on-time delivery of high quality reports at the completion of each study;4.Provide leadership and training to toxicology staff as required;5.Provide input on equipment purchases intended for use in the toxicology program;6.Remain current on appropriate company SOPs (standard operating procedures), GLP (Good Laboratory Practice) regulations, and regulatory guidelines.REQUIREMENTS:1.MS in toxicology or related fields (eg medicine, physiology, molecular biology) and 5-10 years experience in nonclinical research;2.Experience working directly with clients/patients and cooperatively in teams;3.Experience designing/conducting/monitoring toxicology studies;4.Demonstrated successful leadership and excellent written and oral communication skills;5.Computer skills, particularly word processing, spreadsheet, and data acquisition software. 职能类别: 医药技术研发人员 关键字: 周末双休 带薪年假 交通补助 节日福利

联系方式

吴中大道1318号

公司信息

苏州药明康德成立于2006年10月,是药明康德全资子公司,该设施面积达三万多平方米并且目前向全球客户提供符合GLP标准的遗传毒性实验服务,并通过了AAALAC的国际认证; SFDA的GLP认证;欧洲OECD的GLP认证;是全球唯一一家通过全面资质认证的药物安全性评价中心。 同时,苏州药明康德拥有众多获得资格认证的毒理学家和病理学家们,能够为国内外客户提供包括大小动物的急性毒性、长期毒性、药代/毒代、生殖毒性、安全性药理、遗传毒性等药物安全性评价项目以及体内外药物筛选、药理药效研究等临床前安全评价研究服务。

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