Responsible for developing, and maintaining Reltio-based MDM solutions to support clean, unified person and product data across pharmaceutical systems.
Key Responsibilities:
Develop and configure Reltio MDM components including match/merge rules, survivorship, workflows, and data models.
Integrate Reltio with upstream/downstream systems (e.g., ERP, CRM, Clinical platforms).
Implement data quality rules and cleansing logic specific to pharmaceutical data (e.g., product codes, regulatory identifiers).
Support data migration and onboarding activities from legacy systems.
Collaborate with business analysts and data stewards to refine requirements.
Required Experience:
2+ years of hands-on experience with Reltio MDM platform.
Experience with pharmaceutical data domains (e.g., Product, HCP, HCO, Clinical Trial data).
Required Skills:
Robust knowledge of REST APIs, JSON, Reltio Console, and Reltio Integration Hub.
Familiarity with data governance and compliance standards (e.g., GxP, 21 CFR Part 11).