Signal Management Technical Specialist

1 week ago


nagpur, India beBeeTechnical Full time

Job SummaryWe are seeking a seasoned IT specialist with extensive experience in pharmacovigilance systems, particularly signal management and risk management modules.Main ResponsibilitiesAct as a senior subject matter expert for signal management and risk management platforms, owning system functionality, enhancements, and solutioning.Lead requirement workshops, system impact assessments, and end-to-end functional design for PV applications—primarily ArisG Advanced Signals.Drive solution architecture discussions with IT, vendors, and cross-functional stakeholders.System Analysis & DeliveryTranslate business needs into high-quality BRDs, FSDs, user stories, data mapping specifications, integration requirements, and validation documentation.Oversee configuration, release planning, change requests, and production deployments.Conduct root-cause analysis, troubleshoot complex issues, and manage vendor escalations.Support system upgrades, regression testing strategy, and UAT coordination.Process ExpertiseDeep understanding of signal management processes including detection, triage, validation, evaluation, prioritization, and aggregate reporting.Good knowledge and hands-on involvement in risk management plans (RMP) and associated PV risk mitigation workflows.Ensure solutions comply with global PV regulations, audit requirements, and internal quality standards.Collaboration & GovernanceAct as a senior liaison between IT, PV operations, QA, and product vendors.Prepare solution documentation, training materials, and system SOP updates as needed.Provide mentorship/functional guidance to junior BAs and technical team members.Required Skills & Experience12+ years of total experience, with at least 8+ years in pharmacovigilance IT / techno-functional roles.Strong hands-on experience with ArisG Advanced Signals and PV safety systems.Proven expertise in drafting system requirements, data flows, interface specifications, and functional design documents.Strong understanding of compliance requirements (ICSR reporting, aggregate signaling, audit readiness).Excellent verbal and written communication skills, with the ability to work with global stakeholders.About this RoleThis is a unique opportunity to join our organization as a highly experienced IT professional. We offer a dynamic and challenging environment where you can utilize your skills and expertise to drive innovation and excellence in pharmacovigilance systems.


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