1.As the DM point of contact in the study team, review study protocol and provide input from DM perspective.
2.Review DMP and DVP,CRF entry guideline, data transfer agreement and design eCRF and facilitate team review for approval
3.Create and maintain EDC development timeline, and ensure database go-live with good quality per timeline
4.Deliver EDC training to study team if need.
5.Create plans for data cleaning, and ensure data with good quality for statistical analysis
6.Review coding result and facilitate discussion with medical team
7.Provide study status report to the study team, and follow up pending issues
8.Prepare materials for data review meeting
9.Create Data Management Report
10.Database and documents archival
11.CRO oversight in outsourced study Qualification
What you'll need to succeed
1.Education ：Medical/Pharmacy/Computer Science or relevant background
2.Years of Related Experience: 3-5 years Pharm/CRO relevant experience.