基本资料 | ||||||
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姓 名: | 方小姐/女士 | 性 别: | 女 | 出生年月: | 1985-11-20 |
婚姻状况: | 未婚 | 民 族: | 最高学历: | 硕士 | ||
所学专业: | 基因工程 | 毕业学校: | 日本丰桥科学大学 | |||
毕业时间: | 2011-03-23 | 特长概括: | 3年临床试验经验 | |||
团队管理经验: | 无 | 行业工作经验: | 三年或以上 | |||
项目经验: | 化药,化药II期,化药Ⅲ期,化药IV期, | |||||
户 籍: | 上海 | |||||
现所在地: | 国外国外国外 |
自我评价 |
1,影响各级项目组成员和与之谈判的能力 2,有较强的团队精神,良好的人际沟通能力 3,在高压下有独立思考解决工作上出现的问题的能力 4,有较强的语言表达能力和外国语言能力(韩语,日语,英语) 5,与不同专业水平的研究团体相互交流的示范能力 6,影响各级项目组成员和与之谈判的能力 7,区分优先次序和管理多样事务的示范能力 |
求职意向 | |||||
职位性质: | 全职 | 到岗时间: | 3个月以后 | 月薪要求: | 面议 |
求职状态: | |||||
意向岗位: | 临床研究 | ||||
工作地区: | 上海上海市浦东新区,上海上海市静安区,上海上海市黄浦区,上海上海市徐汇区 | ||||
其他要求: |
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培训 |
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工作经验 |
技能专长 |
Perform case processing for serious adverse events, serious and non-serious adverse drug reactions and other medically related project information, such as adverse events of special interest and clinical endpoint ● Review and process serious adverse events, spontaneously reported adverse reactions and/or other medically related information per assigned tasks and study specific procedures. ● Attend project team meetings and teleconferences as required ● Assist with training/mentoring newly hired DSA staff, as requested ● Liaise with Sponsor and attend Sponsor meetings, as required ● Perform safety review of clinical and diagnostic data ● Liaise with investigational site, reporter, and/or Sponsor as necessary regarding safety issues ● Assist the MSS Functional Lead under supervision |
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我的职场风采 |
联系方式 |
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