All Activities relating to study start study conduct and study close out.
Preparation of below documents.
1. eCRF review
2. Preparing Trial derivation plans
3. UAT of Edit checks Reports and DE screens
Development of clinical data testing systems including design documentation implementation and report.
4. End to End CDM activities
5. Perform data management activities on the assigned project in a timely and efficient manner Generate queries to clarify and improve the quality of the data
Test and execute validation procedures.
Experience & Skills Required:
- Relevant of 4 yearsâ€™ experience in Clinical Data Management from any Clinical Phases study start study conduct or close.
- Good working Knowledge about the Databases (Medidata RAVE Oracle Clinical and Inform etc.)