任职要求
1. 计算机、统计、数学、生物科学及医学等相关专业硕士学历
2. 0 到 1 年 CRO或医药公司工作经验
3. 熟练运用 SAS 软件进行数据处理、分析和报告者优先
4. 有 SDTM 、ADaM、 TFL 经验者优先
5. 有熟悉药物开发流程以及临床试验数据处理、分析及报告经验者优先
6. 良好的人际沟通和团队合作能力
7. 良好的英语听说读写能力
8. 能在规定的时间期限内有质量的完成任务
9. 有意愿、有能力不断学习和遵循公司标准流程
10. 如果没有相关经验，愿意接受相关培训
岗位职责
负责临床试验项目数据整理、提取和分析；制作统计分析文档；编写 SAS 程序以生成表格、列表、图表和统计分析结果；对所负责数据、报表及其他结果实行适当的质量控制和核查；负责编写用于检查临床数据的 QC 程序，确保所有临床数据分析结果的一致性和准确性；跨地区团队合作支持公司客户。
Basic Qualifications
1. Master degree in Computer Science, Statistics, Mathematics, Life Sciences, Medical or other related scientific subject
2. 0 to 1 year of relevant programming experience in a clinical development environment
3. Excellent SAS data manipulation, analysis and reporting skills
4. SDTM， ADaM ，TFL experience preferred
5. Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials data
6. Ability to work effectively and successfully in a team environment
7. Excellent oral and written communication skills in English
8 Ability to provide quality output and deliverables, in adherence with challenging timelines
9. Willingness and ability to learn and follow standard processes and procedures
10. Will provide training for employee with 0 year of experience
Key Responsibilities
Programming includes, but is not limited to, the data manipulation, analysis and reporting of primarily clinical trial