- Robust understanding of clinical trial processes and data lifecycle
- Hands-on experience with: o Clinical Metadata Repositories (MDR) o CDISC standards (SDTM, ADaM, CDASH, CT)
- Knowledge of regulatory submissions and compliance (FDA, EMA) Technical & Analytical
- Experience working with data models, metadata schemas, and mappings
- Familiarity with MDR-related platforms or technologies (e.g., graph DBs, metadata services)
- Ability to read and collaborate on technical designs and APIs (functional perspective)
📌 Business Analyst (Noida)
🏢 TCS
📍 Noida
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