Programme Overview
This programme delivers hands-on expertise in managing clinical trial data, ensuring accuracy, integrity, and regulatory compliance.
Students gain real-world exposure to industry tools, workflows, and global standards used in pharmaceutical and CRO environments.
📅 Duration: 3–6 Months
🎓 Eligibility: Any Graduate
💻 Mode: Online
3000+
Students
Students
120+
Hiring Partners
Hiring Partners
95%
Placement Support
Placement Support
Programme Curriculum
Overview of CDM
- CDM Lifecycle
- Roles & Responsibilities
Regulatory Standards
- ICH, CDISC, CDASH
- Data Governance
EDC & CRF Design
- CRF Development
- EDC Systems
Data Cleaning & Validation
- Edit Checks
- Discrepancy Management
Database Lock & Archiving
- Soft & Hard Locks
- Data Archival Practices