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Join our client, a prominent leader in the MedTech Industry.
We are seeking a highly skilled Senior Director, Head of Market Access, Public Affairs & Government Affairs, China. In this role, you will spearhead efforts to enhance market access for innovative therapeutic solutions related to our client's products and ensure success in healthcare policy engagement.
配合诊疗团队,为客户制定营养相关的产品并提供解读,咨询, 市场教育等相关服务。
1. 作为新产品制剂方面的主负责人,为产品开发生产做出重大决策,并组建有关团队;2. 开展新产品固体制剂开发和生产协调工作,确保产品开发和生产的各项工作能够按时按质完成,满足国内外药物注册的相关要求。
某知名上市药企,业务财务伙伴
作为医院运营管理条线负责人,紧密和集团董事长及医疗院长配合,全面负责医院的战略定位、日常运营管理等事务。
根据公司整体策略,统筹整体品牌策略规划,整合各方资源,重点聚焦各产品品牌规划与落地,线上线下多渠道助力品牌声量提升
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。
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.
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.
This is a newly created Head of PMO role for a commercial stage and globally operated biopharmaceutical company. As the PMO, this role will be fully responsible for the portfolio management and product life cycle planning and management.
As the Head of Business Development & Licensing, this role will be fully in charge of the product portfolio development by scouting, evaluating, negotiating and executing the licensing deals for IVD business.
This is a newly created BD& External Innovation Director role for one of the most prestigious multinational pharmaceutical companies. This person will be leading the function to source global opportunities, due diligence and deal execution and ensure that the organisation get access to innovative disease therapeutic targets and technologies across different therapeutic areas.
1. 主导和参与高层互访的各项活动 (70%)2. 政策解读和分析(20%)3. 英文的沟通能力(10%)
负责产品品牌计划与医学策略 根据KOL的需求进行项目合作与管理 维护KOL关系
作为公司的监管合规负责人, 您将负责公司在中国大陆区的全部监管合规战略的制定和实施
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
This position is senior role in the region, reports to CBDO based in the Shanghai and you will be in charge of the international business excluding China mainland and USA. We have an established business across Hongkong, Malaysia, Vietnam and Indonesia.
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