Job Overview Acts as a Lead Medical Writer on straightforward projects (e.g. simpler documents under standard timelines). Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the
Job Overview Provide Trial Master File (TMF) related assistance to study teams. Ensure all work is conducted in accordance with Standard Operating Procedures (SOPs), policies, practices, good clinical practices, applicable regulatory requirements, and meets quality and
Essential Functions • Perform assigned complex administrative tasks to support team members with project execution • Assist in updating and maintaining complex data in systems within project timelines and per project plans • Coordinate the retrieval
工作职责 协助主管处理药品不良反应安全数据，包括：收集和跟踪传入的不良事件（AE）/终点信息、确定传入事件的初始/更新状态、跟踪事件处理完成的时间表等工作。 协助主管管理项目工作流程，包括数据库录入、质量控制活动和药品安全数据报告的生成，准备药品安全提交档案等工作。 其他主管指派的协助任务等。 任职要求 通过日语N2检定，或具备同等程度日语能力；并通过大学英语CET4级或以上。 学历要求为本科及以上，日语专业可，如具备生物、医药相关背景可优先考虑。 能够保证每周至少出勤24-32小时。 实习地点 大连办公室：大连市高新园区腾飞软件园一期西翼10楼 *接受远程和线下实习相结合的方式 顺利通过实习期考核即可优先得到正式offer。 IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create
Job Overview Serve in support level capacity in CDM Validation (Testing) team, to perform testing activities in CDMS environment to provide efficient, quality database as per customer requirement. Essential Functions • Conduct testing activities to validate
Key Responsibilities 1. Manage and coordinate day-to-day support activities, independently handle and resolve complex support cases submitted by clinical trial sites; 2. Provide technical support for medical devices and associated applications at clinical trial sites; diagnose