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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.
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
根据产品注册进度要求,组织协调、督导各部门工作进度,保障申报资料的汇编按时完成;指导注册人员开展相关品种的注册申报,推进已申报品种的注册进度;
Our client is a leading hospitality group with a with a worldwide footprint and diverse business portfolio. The company has a vision to extend a group level strategy and involved health, beauty and wellness related projects. They are currently looking for a General Manager to drive the business initiative across APAC region.
直接对接亿级企业家,拓展国内头部民族品牌
This role needs to be responsible for competitive product analysis, through the collection of competitor data information, market positioning, product functions, user experience and other aspects of comparative analysis, to provide the company with competitive strategy suggestions.
知名大型能源领域公司,寻求IT知名大型能源领域公司,寻求IT 总监一名
知名金融公司,寻求IT总监一名