职责描述：
1. Manage DMs efficiently across studies by setting goals and providing oversight, guidance, mentoring, feedback and performance reviews.
2. To be sensitive on all identifiable solutions for process and technical issues, risk management on any data quality deliverables.
3. Create and implement the Data Management Plans (DMP) to ensure data completeness and accuracy.
4. Perform data cleaning activities including discrepancy management (review of data errors detected from electronic checks and manual checks).
5. Ensure timely set-up of clinical data acquisition and management tools and data validation edit checks.
6. Maintain study tracking to ensure timely CRF retrieval, data entry and data cleaning activities.
7. Ensure integrity of clinical data and update database by issuing and resolving DCFs as necessary.
8. Set-up and test data review listings to verify the quality and completeness of data.
9. Reconcile the patient database with the Serious Adverse Event database and/or third-party data.
10. Document all efforts of data management and file all responsible documents.
11. Lead hiring and training activities as needed.
任职要求：
任职资格
1 Bachelor or master degree in medical, statistics, epidemiology, computer science, or relevant field.
2 Highly efficient with excellent communication skills.
3 Solid knowledge in CDISC standards and FDA/EMA/ICH guidelines is preferred.
4 Effective English verbal and written communication skills.
5 Ability to work effectively in a multi-cultural context as a good team member.

其他信息
语言要求：英语、普通话
行业要求：全部行业