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In collaboration with the Medical Director, supports the development of study protocol and amendments, clinical sections of regulatory documents, including investigator brochures, annual safety update reports; contributes to study documents, including AE section of ICF templates, eCRFs and SAE report forms.
This role is responsible for the analysis of medical research projects conducted by our company
负责国内及境外临床试验的管理和交付。
Collaborate with other functional groups within the company to support milestone achievement and to manage study issues and obstacles. Ensure that Sponsor feedback is communicated and conveyed to other functional groups and action is initiated to address.
Actively manage one or more early or late stage global drug development project teams, executing the program strategy for the specific project, according to the TPP.
引导医院依法执业、规章制度建设,迎检上级卫生行政管理机构的各类专项检查,从医疗行政管控、医院经营需要,患者就医体验等角度不断优化医院制度、就医流程26项,形成规范化、标准化的规范管理。
根据公司的安排,进行研究中心筛选:研究中心的启动访视研究中心启动访视前准备base 北京,天津,上海,长春,长沙,郑州,南京
* 项目立项,制定项目管理计划,确定临床试验进度计划、财务预算等内容,并在项目进行中不断对项目管理计划进行車校和修改,定期汇报试验进度,完成项目进展报告。
base 北京,天津,上海,长春,长沙,郑州,南京
亚洲大型连锁医疗美容集团,专业化国际团队招聘产品,品牌策划负责人
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