✦ Luna Orbit — Science & Research

Associate Director / Director - Pharmacovigilance Scientist - Global Patient Safety

at Eli Lilly

📍 US, Indianapolis IN Unknown 💰 $115K – $169K USD / year Posted March 22, 2026
Salary $115K – $169K USD / year
Type Not Specified
Experience mid
Exp. Years Not specified
Education Not specified
Category Science & Research

This role involves leading safety signal detection and management activities within the global pharmacovigilance team to ensure drug safety and regulatory compliance.

  • Lead safety signal detection
  • Evaluate safety data
  • Collaborate on benefit-risk assessments
  • Manage regulatory safety reports
  • Conduct literature reviews

The technical scope includes analyzing safety data from sources like FAERS and VigiBase, applying epidemiologic and statistical methods, and preparing safety reports for regulatory agencies.

The ideal candidate is a scientific professional with expertise in pharmacovigilance, signal detection, and safety data evaluation, with strong analytical and regulatory knowledge in the healthcare industry.

PharmacovigilanceSignal DetectionSafety Data EvaluationRegulatory KnowledgeData Analysis
EpidemiologyRisk ManagementMedical WritingBenefit-Risk AssessmentLiterature Review
FAERSVigiBaseRegulatory DatabasesEpidemiologic ToolsStatistical Software
PharmacovigilanceSignal DetectionSafety Data EvaluationEpidemiologyStatistical MethodsRisk ManagementRegulatory ReportingMedical ReviewData AnalysisBenefit-Risk Assessment
PharmacovigilanceSignal DetectionSafety Data EvaluationEpidemiologyStatistical MethodsRisk ManagementRegulatory ReportingMedical ReviewData AnalysisBenefit-Risk Assessment
Critical ThinkingDecision MakingCollaborationProblem-solvingCommunication
Industry Healthcare & Medical
Job Function Ensuring drug safety through safety data analysis and signal management
Role Subtype Pharmacovigilance Scientist
PharmacovigilanceSignal DetectionSafety Data EvaluationEpidemiologyStatistical MethodsRisk ManagementRegulatory ReportingMedical ReviewData AnalysisBenefit-Risk Assessmentpharmacovigilancesignal detectionsafety data evaluationregulatory reportingepidemiologyrisk managementmedical reviewdata analysisbenefit-risk assessmentliterature review

Lack of pharmacovigilance experience, No experience with safety data analysis, No understanding of regulatory safety requirements

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