长沙招聘

岗位职责：
1.Study Management
   A.Protocol Evaluation
   B. Site Preparation
   C.Close-Out
2.Project Activities
   A.Investigational Product Accountability
   B.Laboratory Issues
   C.Adverse Events
   D.Responsibilities and Obligations
3.Subject Coordination
   A. Recruitment
   B. Informed Consent
   C. Screening/Scheduling
   D.Study Conduct
4.Documentation and Administration
   A. Case Report Forms (CRFs)
   B. Source Documentation
   C. Financial/Budgetary Issues
5.Project Management
   A.Lead project team and act as focal contact with sponsor.
   B. Provide protocol specific training to team members as necessary.
   C. Supervise all aspects of CRC’s clinical study site management activities.
   D.Conduct QC if needed.
   E.Track and ensure study budget according to the agreement.
6.People Management
   A. Monitor the overall performance of assigned CRC team and provide regular reports to line management.
   B.Effectively lead, manage, coach, mentor and develop direct reports in CRC team.
   C. Support the planning and delivery of training programme for CRC team to develop technical skills and ensure professional competency.
任职要求：
1. A Bachelor Degree in a medical, health, or science related are, or a nursing degree.
2. Minimum of 1 years related experience in clinical research.
3. Thorough understanding of all relevant ICH-GCP guidelines and regulations.
4. Good verbal and written communication skills.
5. Good team player, self-motivated and attention to details.
6. Good customer focused sensitivity towards internal and external customers.
7. Must be able to travel.

    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。