gence, analytics, SQL, and Pharmacovigilance (PV) application support.
The candidate will be responsible for developing and supporting OBIEE/OAS reports, dashboards, analytics, and metadata models, while working closely with Pharmacovigilance and Drug Safety teams. The role involves analyzing PV data, validating reporting outputs, troubleshooting business intelligence solutions, and ensuring accurate delivery of safety-related reports and analytics.
Professionals should have hands-on experience with OBIEE Report Development, Oracle SQL, OBIEE/OAS Dashboards, RPD, Metadata Layer, Pharmacovigilance, Oracle PV Application Support, PV Data Analysis, and Data Validation. Knowledge of GxP and Computer System Validation (CSV) requirements within regulated pharmaceutical environments is highly preferred.
The role also involves collaborating with global business users, Drug Safety teams, IT stakeholders, and technical teams to gather requirements, resolve production issues, enhance reporting solutions, and ensure compliance with applicable pharmaceutical and pharmacovigilance standards.
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