
Detail-oriented Clinical Operations and Data Quality professional experienced in data review, documentation management, and compliance monitoring within pharmaceutical environments. Managed GDP-compliant turnover packages, verified regulated supply transactions, and ensured data integrity and audit readiness. Skilled in investigating discrepancies, conducting root cause analysis, and collaborating with cross-functional teams in GMP/GDP settings.
Clinical Data Cleaning
Data Validation
Data Integrity
Data Review
Data Reconciliation
Query Management
Clinical Trial Support
Data Collection
Data documentation management
Database Lock Preparation
UAT Support
Root Cause Analysis
KPI Monitoring
Audit Readiness
SOP Compliance
ICH-GCP
GMP
GDP
Risk Assessment
CAPA
Regulatory Compliance
Vendor Collaboration
Stakeholder Management
Document Management
Project Management