About the role
Experience: 10 to 15 years
Required Skills & Competencies Domain & Functional Strong 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)Tools Requirements & documentation: Jira| Confluence| Word| Excel Design & validation: Figma| Visio Data & metadata concepts: SQL (read-level understanding preferred)Soft Skills Excellent communication and stakeholder management skills Strong analytical and problem-solving mindset Ability to work in cross-functional| global teams Detail-oriented with a structured| quality-first approach Preferred / Nice to Have Experience working on enterprise MDR implementation