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Required Skills & Experience
• 3+ years of experience working with RXLogix platforms
• Hands-on experience supporting system implementations or major enhancements
• Strong understanding of pharmacovigilance processes (case processing, signal detection, aggregate reporting)
• Experience working with safety databases (e.g., Oracle Argus or similar)
• Ability to translate business requirements into technical/system configurations
• Strong communication skills and experience working with cross-functional pharma teams
Nice to Have Skills & Experience
• Experience with specific RXLogix modules (PVAnalytics, PvNet, Signal Management)
• Prior experience in biotech/pharma environments (bonus if supporting commercial-stage orgs)
• Familiarity with data visualization/reporting tools (SQL, Power BI, etc.)
• Experience supporting validation documentation (CSV lifecycle, IQ/OQ/PQ)
Job Description
We are seeking an experienced RXLogix Consultant to support the implementation and optimization of pharmacovigilance systems within a leading biopharmaceutical organization. This individual will partner with cross-functional stakeholders to configure, deploy, and enhance RXLogix solutions in alignment with safety and regulatory requirements.
Key Responsibilities:
• Support end-to-end implementation of RXLogix solutions (e.g., PVAnalytics, PvNet, Signal Management modules)
• Collaborate with Safety, Pharmacovigilance, and IT stakeholders to gather business requirements and translate into system configurations
• Configure and customize RXLogix applications to meet business and regulatory needs
• Assist with data integration, validation, and migration activities across safety systems (e.g., Argus, ARISg)
• Develop and execute testing strategies (UAT, validation, defect resolution)
• Provide training and documentation to end users and business teams
• Support post-go-live activities including enhancements, troubleshooting, and user support
• Ensure compliance with GxP, FDA, and global pharmacovigilance regulations
Job ID: 149084501
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