上海相关职位： （高级）产品技术专员-骨科-上海 Western Blot产品工程师 Western Blot产品工程师 医院销售经理 药物合成研究员 医疗产品经理/主管 机械制图工程师 助理招标工程师（应届生，文科类专业即可） 标本技术员 研发项目经理
周边城市招聘： 上海 浙江 安徽 广东 山东 河北 重庆 北京 江苏 湖南
企业入驻日期： 2017-11-09
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无工作经验 -
本科 -
招1人 -
11-09 发布
- 五险一金
- 补充医疗保险
- 定期体检
- 弹性工作
- 免费班车
- 补充公积金
职位描述
职位描述： Covance Shanghai is hiring Regional Study Coordinator. This role has a high involvement in client engaging across Asia Pacific. Gain the helicopter perspective from both the client and business, as well as develop the expertise within the clinical trial The Regional Study Coordinator is responsible for the successful delivery of alloperations (regional monitoring included) of a clinical study in their specific area of the world, acting locally as the appointed Liaison between Global Project Management department and Client Representatives on one side as well as other CCLS departments involved in the clinical study on the other side, to ensure the successful management of regional study responsibilities. The Regional Study Coordinator may ensure as well the communication with the Client when this task is being delegated by the Global Study Manager. Regular communication is essential with the appointed Global Study Manager who is accountable for the entire protocol. This position must be in compliance with the CCLS Global Project Management strategy and deliver outstanding customer satisfaction and performances.Responsibilities/Duties1. Act as regional liaison between Global Study Manager and various CCLS departments involved in the study2. Act as regional liaison between assigned Client representatives (eg. CRA, Site Monitors) and the corresponding local CCLS platform; occasionally, the Regional Study Coordinator can represent Global Study Manager in interactions with the main client contact3. Close collaboration with the Global Study Manager for all study related aspects that are pertaining to the corresponding local platform and through all study stages, from set-up to closure4. Review the study Statement of Work to ensure local feasibility and make appropriate recommendations to the Study Design Lead5. Ensure a detailed knowledge of the SOW specifications and very good understanding of how the SOW specifications impact every operational aspect of the clinical trial6. Manage day-to-day local study related activities, especially logistics, monitoring and study supplies, keeping the Global Study Manager informed of any study development7. Monitor, track and provide resolution to all local studies issues and complaints, keeping the Global Study Manager in the communication loop8. Responsible for implementing monitoring and setting up of local performance metrics and taking corrective actions when needed.9. Liaise with the Global Study Manager for any tasks assigned to the Regional Study Coordinator as part of the Global Monitoring Plan10. Demonstrate ability to work in a matrix environment where some task assignments are being channeled down to be dealt with by Regional Study Coordinators while other task assignments will need to be delegated by Regional Study Coordinators to other functional groups; demonstrate flexibility in handling both categories of tasks11. Participate in functional meetings (eg. CLFs) and provide input, keeping processes up to date12. Comply with CCLS Global Project Management strategy13. Support a culture of continuous improvement, quality and productivity14. Other duties as assignedIdeal Candidates have 2 or 3 years’ customer service or project management experience in Clinical Trials function, have worked on Neuroscience, Immunology & infectious diseases studies, have some bid defence and costing experience, and are ready for a new exciting challenge! Education/Qualification:You should typically be qualified to degree level or equivalent in one of the life sciences.Language Speaking:Mandarin (Must); English Required (Must in writing and reading, Oral English should be above average)Experience:2 years customer service experience, preferable in pharmaceutical industry (Education may be substituted for experience) 职能类别： 其他 其他 关键字： 项目管理 临床试验 CTA CRC
联系方式
张江高科技园区李冰路151号 6号楼
公司信息
Why Covance? At Covance, you will join like-minded professionals who, together, build our reputation as one of the world's largest and most respected contract research organizations. In choosing Covance, you will be part of a dedicated team that makes a difference in helping to deliver life-saving and life-enhancing medicines to people around the world. We Offer Covance’s ongoing success offers team members unsurpassed growth and career development opportunities. At Covance, we help make the miracles of medicine a reality. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career. There is no better time to join us!
