inVentiv Health Clinical,是一家全球排名前五的CRO服务供应商公司,致力于为生物医药及医疗器械公司提供全球研发服务。我们可以提供从单个项目到整个专业职能团队配备的专业服务，包括专注到细分治疗领域的，I-IV各期的临床研发，生物分析以及战略资源整合等相关专业服务。目前盈帆达医药在全球36个国家拥有超过7000名全职员工，正在为各类客户加速其高品质医药的研发进程而努力工作。 目前我们在以下城市需要CRA： 上海、北京、成都、广州 、香港、台湾如果你具备以下条件？ · 生命科学/生物医药相关专业本科（学士）及以上学历 · 至少1年CRA工作经验，有肿瘤临床研究实地监查工作经历者优先 · 有其他治疗领域的工作经验也会被考虑 · 有外资药厂或国际多中心项目经验者优先 · 较强的人际沟通与组织管理技巧 · 了解并掌握ICH/GCP相关知识 我们将提供与职位相匹配的： · 具有行业竞争力的优厚薪资福利待遇 · 在行业领先和创新的公司体系内，为你的个人职业进步提供各种培训和发展支持 · 有成功感及价值感的良好工作环境 主要的工作职责： · 为临床试验的中心选择提供专业服务，参与执行中心选择及标准评价工作 · 在研究中心与项目管理团队之间保持良好有效的沟通交流，为研究者提供有价值的建议和帮助 · 准备、收集和核查所有研究中心相关的文件，解决各种与之相关的问题 · 执行中心启动及培训的相关工作 · 核查并管理研究中心的原始数据，及时处理各类试验相关的问题 · 执行中心关闭相关程序 · 按要求及时完成监查报告 · 指导并培训新加入研究的相关人员 · 确保研究中心的进展符合研究计划进度要求 · 确保研究中心的各项工作符合GCP，ICH及SOP等各项法规制度要求 · 跟踪管理研究预算 如果您对该职位感兴趣，请将你新的个人简历及项目经验以WORD格式发送至以下电子邮箱地址：lingfeng.yang@inventivhealth.com感谢您的关注！Clinical Research Associates inVentiv Health Clinical, formly PharmaNet/i3, is a leading provider of global drug development services to pharmaceutical, biotechnology, generic drug, and medical device companies, offering therapeutically specialized capabilities for Phase I-IV clinical development, bioanalytical services, and strategic resourcing from a single clinical professional to an entire functional team. With 7,000 passionate employees in more than 36 countries, inVentiv Health Clinical works to accelerate high quality drug development programs of all sizes around the world. Do you have the required skills?· Bachelor’s level degree in pharmacy or life sciences.· Minimum 1 years as a CRA with hands on monitoring experience in oncology preferred · Other Therapeutic experience will be considered· Global studies experience is essential· Ability to communicate in English· Strong interpersonal and organizational skills· Thorough ICH/GCP knowledgeGreat Benefits with the role· Competitive remuneration package with excellent benefits· Commitment to your development and training, with the opportunity to progress your career within a market leading and innovative organization.· Opportunity to work within a successful and rewarding environment.Responsibilities· Participate in site selection process, perform evaluation and make recommendation for trial inclusion.· Facilitate communication between sites and line functions and increase value proposition to investigators.· Facilitate preparation and collection of site level documents, resolve problems as required.· Execute site initiation and training.· Manage data at the site, resolve technical and content issues· Implement closeout activities.· Complete and generate study monitoring reports.· May act as a mentor to new associates.· Ensure site activities in line with milestones and project timelines.· Ensure compliance of GCP, ICH and SOP.· Review and manage study budgets.We offer exciting opportunities, competitive packages, ongoing support, career development, training opportunities and flexible career options at leading global companies including the top biopharmaceutical MNCs to our employees.