Domain & Functional • Solid 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)