长沙招聘

职位描述：
1、工作职责
* Prepare integrated clinical trial report both in English and Chinese in collaboration with project team members, based on results from clinical trials according to GCP, SOPs, and external guidelines.
* Prepare abstracts, posters, slide presentations, and publications in collaboration with investigators, marketing, and clinical team members based on results from clinical trials.
* Give professional input to publications prepared by doctors.
* Provides information collection, literature retrieval and the corresponding support for clinical studies and the submission of registration documents
* Provides relevant literature retrieval for products, the progress of clinical studies and other information
* Reports adverse drug events in accordance with national regulations and internal establishments, including the medicine both under clinical research and post marketing.
* To maintain the Office Library.
* To maintain the SOP.
* Maintain up-to-date knowledge and competencies within relevant therapeutic and professional areas


2、招聘要求
* Bachelor's degree or above in Medical science.
* Fluent English on both written & verbal.
* 2 years of experience in clinical is prefer.
* Ability to accurately and clearly present clinical data as well as strong verbal and written
* Good communication skills and teamwork spirit
* Ability to work independently, to handle multiple tasks simultaneously.
* Previous working experience in pharmacovigilance. 举报 分享

    诺思格（北京）医药科技股份有限公司是国内专业领先，规模较大的临床研究合同组织（CRO）之一，总部设在北京，办事处设在上海、长沙、广州、武汉、成都、西安、哈尔滨、南京、沈阳、天津、长春、杭州、合肥等省会城市；在国内覆盖60余个城市，在亚洲覆盖6个国家与地区，已与200余家机构，450余家医院及600多个科室合作，目前已为260多位国内外客户提供国际标准的临床研究外包服务。业务涵盖新药评估与咨询、注册事务、临床试验实施、数据管理和统计分析、医学事务及培训等全方位服务。

“服务医药 服务健康”，详情请登录公司主页： *****************

接收简历邮箱：hr@rg-pharma.com（邮件主题：城市+岗位名称+本人姓名）

【子公司】苏州海科医药技术有限公司为诺思格（北京）医药科技股份有限公司的子公司，子公司成立于2015年01月14日，地址位于苏州工业园区裕新路108号4楼，经营范围包括生物技术开发、生物检测技术服务、会务服务，详情请登录公司主页：*******************************/

【子公司】南京艾科曼信息技术有限公司，专攻于临床研究领域中的数据管理和统计分析环节，全面移植美国CRO的质量标准及管理体系，一步到位与国际CRO行业接轨。同时，服务质量获得欧美主要药厂的认证。自成立以来已完成300余项临床项目，其中部分已经获得美国FDA及欧洲EMEA通过。率先使用国际标准数据管理系统，所有高管均有在美国相关行业从业10年以上经验。总部位于北京，在上海、南京、成都、武汉、合肥等省会设有办公室。