✦ Luna Orbit — Data & Analytics

Associate Director - Statistics (Clinical Trial)

at AbbVie

📍 South San Francisco, CA Unknown Posted March 13, 2026
Type Full-Time
Experience senior
Exp. Years 6+ years
Education MS (with 10+ years of experience) or PhD (with 6+ years of experience) in Statistics, Biostatistics, or Mathematics
Category Data & Analytics

This role provides statistical leadership for clinical development projects, focusing on trial design, analysis, and regulatory documentation.

  • Lead statistical support for clinical projects
  • Develop protocols and analysis plans
  • Ensure regulatory compliance
  • Mentor junior staff
  • Collaborate with cross-functional teams

Technical scope includes statistical analysis, protocol development, regulatory submissions, and data presentation within clinical trial environments.

The ideal candidate is a senior statistician with extensive experience in clinical trial data analysis, protocol development, and regulatory submissions, capable of leading statistical strategies for complex projects.

MS in StatisticsBiostatisticsor MathematicsExperience in clinical trialsStatistical strategy developmentProtocol and analysis plan developmentRegulatory document review
Experience with regulatory submissionsMentoring junior staffExternal collaboration
Statistical SoftwareRegulatory Submission Tools
StatisticsBiostatisticsMathematicsClinical TrialsStatistical StrategyProtocol DevelopmentAnalysis PlansRegulatory SubmissionData PresentationStatistical Software
StatisticsBiostatisticsMathematicsClinical TrialsStatistical StrategyProtocol DevelopmentAnalysis PlansRegulatory SubmissionData PresentationStatistical Software
communicationleadershipmentoringcollaborationproblem-solving
Industry Healthcare & Medical
Job Function Clinical trial statistical leadership
Role Subtype Senior Statistician
StatisticsBiostatisticsMathematicsClinical TrialsStatistical StrategyProtocol DevelopmentAnalysis PlansRegulatory SubmissionData PresentationStatistical SoftwareMentoringCollaboration

No experience in clinical trials, Lack of advanced degree in relevant field, No experience with regulatory submissions

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