临床数据经理
Clinical Data Manager
在Clario，隶属于Thermo Fisher Scientific。作为临床试验终点技术领域的全球领导者，加入我们，帮助改善患者结果的证据生成方式。作为临床数据经理，您将审查和评估来自赞助方临床试验影像部分的临床数据，涵盖多种治疗领域，确保数据生命周期中的准确性、合规性和质量。
我们提供的福利
- 具有竞争力的薪酬和激励措施
- 住房公积金和医疗保险
- 丰富的员工活动和本地活动
- 现代化的办公空间和远程工作灵活性
您将负责的工作
- 完成所负责研究的所有数据管理交付物
- 按要求参加客户会议并参与讨论
- 理解研究实施和数据收集的要求
- 与项目团队合作，制定研究特定的编辑检查标准
- 制定、执行和审查编辑检查；解决数据不一致问题
- 保持研究文档的有序、完整和最新
- 执行研究设置，包括TF设计、数据库结构和规范
- 协调并记录从外部来源接收和处理电子或辅助数据的过程
- 审查数据中的错误和不一致之处；协作解决问题
- 跟踪未决问题并跟进直至解决
- 确保CDM活动符合监管指南
- 遵守SOP和部门标准；协助更新SOP
- 为团队努力做出贡献，并探索增加价值的机会
- 通过培训保持技术和行业知识
我们寻找的人选
- 生命科学或相关领域的学士学位（或同等经验）
- 在制药、生物技术或CRO行业具有3年以上临床数据管理经验
- 熟悉关系型数据库的组织和验证
- 熟悉SAS者优先
- 熟练使用Word、Excel和Access者优先
- 了解临床试验术语者优先
- 强大的问题解决能力和细致入微的注意力
- 能够独立工作并在团队中协作；适应不断变化的优先事项
- 优秀的沟通和人际交往能力
- 强大的文档编写和组织能力
- 工作地点在印度或能够从印度工作（提供远程/混合选项）
在Clario，我们的使命是通过解锁更好的证据来改变生活。这是一个团结并激励我们的事业。这就是我们工作的理由—
查看英文原文
At Clario, part of Thermo Fisher Scientific. Join us as a global leader in clinical trial endpoint technology and help transform evidence generation for better patient outcomes. As a Clinical Data Manager, you will review and evaluate clinical data generated from the imaging portion of sponsor clinical trials across diverse therapeutic areas, ensuring accuracy, compliance, and quality throughout the data lifecycle.
What We Offer
- Competitive pay and incentives
- Provident fund and medical insurance
- Engaging employee programs and local events
- Modern office spaces and remote work flexibility
What You’ll Be Doing
- Perform all data management deliverables for assigned studies
- Attend and participate in client meetings as requested
- Understand requirements for study implementation and data collection
- Collaborate with project teams to develop study-specific edit check criteria
- Define, run, and review edit checks; resolve discrepant data
- Maintain organized, complete, and up-to-date study documentation
- Perform study setup including TF design, database structure, and specifications
- Coordinate and document receipt and processing of electronic or ancillary data from external sources
- Review data for errors and inconsistencies; collaborate to resolve issues
- Track outstanding issues and follow up until resolution
- Ensure CDM activities comply with regulatory guidelines
- Adhere to SOPs and departmental standards; assist in SOP updates
- Contribute to team efforts and explore opportunities to add value
- Maintain technical and industry knowledge through training
What We Look For
- Bachelor’s degree in Life Sciences, or related field (or equivalent experience)
- 3+ years of experience in clinical data management within pharma, biotech, or CRO industry
- Working knowledge of relational database organization and validation
- Familiarity with SAS desirable
- Proficiency with Word, Excel, and Access preferred
- Understanding of clinical trial terminology desirable
- Strong problem-solving skills and attention to detail
- Ability to work independently and in a team setting; adaptable to changing priorities
- Excellent interpersonal and communication skills
- Strong documentation and organizational abilities
- Based in or able to work from India (remote/hybrid options available)
At Clario, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.
Originally posted on Himalayas