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.
Experience & Skills Required:
Relevant experience from 1 years 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.)
Bio Technology & Life Sciences , Hospitals/Healthcare/Diagnostics
Health Care , Pharmaceutical/Biotechnology
Documentation/Medical Writing , Other Pharma