- 3-4年经验
- 硕士
- 招1人
- 11-09 发布
- 五险一金
- 年终奖金
- 定期体检
- 免费班车
- 专业培训
职位描述
职位描述: Key accountabilities: 1.Study Implement:?Comply with the task arrangement, responsible for study procedures including: protocol reading, understand the protocol details, preparation work, dose animals, collect and processing samples expertly?Responsible for clinical observation and study record, report any issues occurred during the study to PI timely ?Substitute associate PI as associate PI’s absence?Raw data collection1.Improve theory knowledge and technique skills. 2.ComplianceLearn company compliance and comply with it.Scope of the job. 2.Responsible for study implement:?Play Associate PI's role if needed to support PI's work ?Comply with the task arrangement, read to understand the protocol, and know the protocol details ?Support Associate PI's arrangement to prepare labels, tubes, syringes, etc.?Comply with task arrangement and study protocol, dose animals expertly?Comply with task arrangement and study protocol, collect and processing3.Samples expertly ?Raw data, record and tracking management:?Familiar with abnormal appearance of animals undergone, and keep relevant records precisely and timely ?Record any issues occurred during the study, and report to Associate PI or PI timely ?Make sure the study records to be precise, clear and trackable 4.Training:?Improve technique skills level by training, practicing, learn some PK fundamentals and share with others 5.For compliance, learn and ensure no compliance violation.Core business/Functional skills and education.1.Be equipped with college degree or above, have more than 5 years working experence in dog and monkey PK area. 2.Possess pharmacy, veterinary medicine, or biology related major as professional background. 3.Have a strong sense of responsibility, and work actively4.Keen to improve skills and PK fundamentals, and have a strong will in finding new ways to improve work quality 5.Be skillful at variety of technique methods and willing to share with others 6.Be influent in reading English protocol7.Having strong team work spirits and willing to work overtime 职能类别: 医药技术研发人员
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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