Project Coordinator

Notice to Candidate: Location of this position is Shunyi, Beijing

JOB DESCRIPTIONS

1. To support the studies in the clinical planning and implementation of overall project plans, scopes, and schedules-ensuring deliverables are made on time and within project budget. Provide all assigned/clients support (as needed) throughout the duration of an assigned study. 支持临床试验项目整体项目计划、范围和时间表的规划和实施，确保在项目预算内按时完成可交付成果。在特定项目的整个过程中（根据需要）完成指派任务/客户支持。

2. Be instrumental in the delivery of services and manage the day-to-day study coordination work to meet the needs of clients. Act as a Day-to-day point of contact with client as part of the Project Team. 致力于提供服务，并管理日常项目协调工作，以满足客户的需求。作为项目团队的一部分，担当日常客户联系人。

3. Assist Project Managers and the Director, delivery in managing workflow and delivering on a wide variety of clients requests across assigned studies. 协助项目经理和总监，管理工作流程，并在指定的研究中满足各种客户要求

4. Effectively communicate project expectations and status to team members and stakeholders in a timely and clear manner, and proactively manage changes in project scope, identify potential crises, and devise contingency plans. 及时、清晰地向团队成员和利益干系人有效传达项目期望和状态，主动管理项目服务内容的变化，识别潜在的危机，制定应急计划。

5. Develop and strengthen client relationships through demonstration of successful launches of study implementation. 通过成功启动新项目来发展和加强客户关系。

6. Strong to build, develop, and grow business relationships vital to the success of the project. 牢固地建立，发展和增长对项目成功至关重要的业务关系。

7. To support in foreseeing as many project-related risks that may occur, resolving conflicts and breaking down barriers throughout the process. 尽可能多地预见可能发生的与项目相关的风险，解决冲突并打破整个过程中的障碍。

EDUCATIONAL & QUALIFICATIONS

1. Bachelor's Degree is essential and in Life Sciences preferred.本科学历以上，优先考虑生命科学相关专业。

2. Have at least 1 year of experience as a Research Coordinator in a clinical research setting. OR 至少1年以上临床研究领域研究协调员工作经验。或

3. Have relevant experience working in clinical trials, either as a Site Coordinator or from the Sponsor or CRO side. OR拥有临床试验领域相关工作经验，代表申办方或CRO担任现场协调员。或

4. Minimum 1 year of total experience in project/product coordination in the clinical trials industry or have additional certification for work Clinical Research such as Clinical Research Graduate Certificate, Good Documentary Practice (GDP), Research Ethics. 在临床试验业务领域1年以上项目/产品协调经验或已获得临床试验相关证书，如临床试验毕业证书、GDP，Research Ethics

5. Good command of communication skill and team player, integrity and honest. 良好的沟通协调能力和团队合作能力，正直诚实。

6. Fluent in English reading and writing with average listening and speaking skills. 英语读写流利，听说良好。