TOX study director / Tox Director 苏州

月薪： 1.5-2万/月

该公司所有职位
  • 3-4年经验
  • 硕士
  • 招3人
  • 11-09 发布
  • 五险一金
  • 免费班车
  • 交通补贴
  • 员工旅游
  • 餐饮补贴
  • 专业培训
  • 出国机会
  • 年终奖金
  • 绩效奖金
  • 定期体检

职位描述

职位描述： Functions as a Study Director., the Assistant director will have performed satisfactorily for at least a-12 month period* in assisting in all aspects of the Study Director role (as defined in the Position Description for the Scientist) and will have been judged by the Scientific Director and Director of Toxicology to be competent to be a Study Director.2. Functions as a junior study manager under the guidance of the Study Director. The Assistant Scientist is not permitted to be the authorizing signatory on any driving document, but can be involved in study performance as follows:a) Participate in preparation of schedule of study activities within contributing departments.b) Able to plan and coordinate upcoming studies.c) Able to monitor and control studies and problem solve.d) Able to implement and monitor appropriate techniques of test article administration.e) Aware and conversant with all associated SOPs.f) Fully aware of appropriate Good Laboratory Practices.g) Prepare study schedules, protocols, protocol amendments and draft reports.h) Limited exposure to client contact with supervision of Study Directori) Satisfactory performance in Toxicology/Other Examinations required for progression to Scientist I.3. Familiarization with appropriate regulations, guidelines and guidances.4. The Assistant Scientist must ensure that a safe working environment is maintained by all project related staff through the observance of safety procedures, the use of protective clothing or equipment and by the distribution of relevant safety information.5. This may be period may vary depending on experience and the applicants apptitudeQualificationsPh.D., D.V.M., M.Sc., or B.Sc. in Toxicology or related biological discipline or suitable other experience. 职能类别： 生物工程/生物制药

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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