✦ Luna Orbit — Healthcare & Medical

Associate Director, Statistics

at AbbVie

📍 North Chicago, IL Unknown Posted March 24, 2026
Type Not Specified
Experience mid
Exp. Years Not specified
Education Not specified
Category Healthcare & Medical

This role involves providing statistical expertise for medical affairs and health technology assessment activities, including study design, data analysis, and regulatory interactions.

  • Provide scientific and statistical expertise
  • Design and review protocols
  • Evaluate databases and RWE studies
  • Support HTA submissions
  • Collaborate with cross-functional teams

The position requires expertise in biostatistics, clinical trial analysis, real world evidence, and regulatory compliance, utilizing statistical tools and methodologies.

The ideal candidate is a mid-level biostatistician with experience in clinical trial design, real world evidence, and regulatory interactions, capable of leading scientific collaborations and providing expertise for HTA submissions.

BiostatisticsClinical researchStudy designRegulatory interaction
Real world evidenceVendor oversightScientific presentation
Statistical softwareData analysis tools
biostatisticsclinical trialreal world evidencestudy designregulatoryscientific researchvendor oversightdata analysismedical affairsHTA
BiostatisticsMathematicsClinical trial analysisReal world evidenceStudy designStatistical methodologyRegulatory interactionScientific researchVendor oversightData evaluation
LeadershipCommunicationScientific expertiseCollaborationProblem-solvingRegulatory awarenessAnalytical thinking
Industry Healthcare & Medical
Job Function Biostatistics and scientific support for healthcare evidence generation
Role Subtype Medical Research & Biostatistics
biostatisticsclinical trialreal world evidencestudy designregulatoryscientific researchvendor oversightdata evaluationmedical affairsHTAhealth technology assessmentRWERWDmedical affairs researchscientific publicationsregulatory interactiondata analysis

Lack of experience in clinical research, No background in biostatistics, No regulatory experience

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