Senior Clinical Research Associate, China

Senior Clinical Research Associate, China Who We Are Emerald Clinical Trials is a global leader in clinical research, partnering with over 160 biotech companies and 15 of the world’s top 20 pharmaceutical firms. Headquartered in Singapore, we combine scientific excellence with operational expertise to deliver end-to-end clinical trial solutions across all phases, offering Phase I-IV and real-world studies . With over 25 years of experience and a world-renowned focus in renal research , Emerald Clinical has helped drive medical breakthroughs through deep scientific insight, flawless execution, and an unwavering commitment to quality. Global Expertise. Local Insight. Real Impact. Emerald Clinical is where science, speed, and strategy come together to transform healthcare. For over 25 years, we have led the way in clinical research, combining global reach with deep Asia-Pacific expertise and unparalleled local insight to deliver smarter trials and stronger outcomes. Our 800+ employees that span across Asia-Pacific, Europe, and the Americas are embedded in communities worldwide. We drive faster recruitment, deeper patient engagement, and meaningful results that move medicine forward. About the Role The Senior Clinical Research Associate (SCRA) is a member of the Clinical Operations group at Emerald Clinical. The Clinical Operations group is responsible for site management, monitoring tasks, and the operational support of clinical trials. The group allocates resources to projects as appropriate to assist with the implementation of project plans and to ensure compliance with regulatory requirements and Standard Operating Procedures (SOPs). Key Responsibilities 主要职责 Conduct study site selection, initiation, monitoring, close-out visits and study documents management in accordance with the trial protocol, contracted scope of work, Standard Operating Procedures (SOPs), and Good Clinical Practice (GCP) requirements. 依据试验方案、合同约定工作范围、SOP和GCP的要求进行研究中心筛选、启动、监查、关闭访视以及研究文件管理等工作。 Requirements 职位要求 Bachelor’s degree or above in a medicine/health-related discipline. 医药相关专业本科及以上学历。 Minimum of 4 years of clinical trial monitoring experience; experience in nephrology and oncology projects is preferred, as is prior experience with foreign CRO/pharma companies. 具有4年及以上临床试验监查经验，有肾病或肿瘤领域项目经验者优先，有外资工作经验者优先。 Strong learning, organizational, and coordination skills, with excellent written and verbal communication abilities. 具备良好的学习和组织协调能力，清晰的书面和口头表达能力 High level of integrity, strong sense of responsibility, and solid execution capabilities. 为人诚实正直，具备较强的责任心和执行力 Proficient in standard office software applications. 熟练应用各类常用办公软件 CET-6 or equivalent English proficiency, with fluent reading and writing skills. 英语六级或同等水平，读写流利。 Why Join Us? At our core, Emerald Clinical Trials is committed to transforming clinical research by putting people first—both patients and our employees. By joining our team, you’ll be part of a global network of passionate professionals working together to deliver better research and outcomes for millions worldwide. Here’s what makes us stand out: • Purpose-Driven Work : You’ll contribute to clinical trials that genuinely improve lives, with a focus on therapies in renal, cardiometabolic, and oncology. • Global Reach, Local Expertise : Our teams connect with local communities, building trust and meaningful engagement for every trial. • Collaboration and Innovation : Work in a culture that values diverse perspectives and creative solutions to solve global health challenges. Interested? Apply now and help us achieve our mission to improve the health of millions worldwide. We are an equal-opportunity employer and encourage applications from all qualified candidates. Department Clinical Operations Role Clinical Research Associate Locations China - Beijing Remote status Hybrid