Having 7+ years of experience in the Clinical Data Management field.
- Applied critical analysis and exceptional communication skills to design data collection solutions for clinical trial sponsors.
- Knowledge in Medical Coding with MedDRA and WHO Drug
- Successfully designed Edit Checks, and Query logic and conducted User Acceptance Testing (UAT).
- A considerable amount of experience with phases I through III of clinical trials using EDC (electronic data capture).
- Well-versed in ICH-GCP and 21 CRF Part 11 guidelines.
- Working experience in developing Data Transfer Agreements with external vendors.
