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Johnson & Johnson

Senior Principal Scientist, Biostatistics

Johnson & Johnson

. Lead major portions of biostatistical research and development projects independently .

Posted 11/11/2026full-timeUnited StatesSenior💰 $140,000 - $241,500 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates advanced statistical expertise in biostatistical research and development, with proficiency in R and SAS for data analysis and visualization. Capable of leading innovative methodologies, mentoring teams, and ensuring compliance with regulatory standards in pharmaceutical research.

Highest-signal resume keywords
Master’s Degree In StatisticsPhD In StatisticsAdvanced Data Analytics ExpertiseFull Proficiency In R And SASKnowledge Of Statistical Methodologies

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Biostatistical ResearchExperimental DesignStatistical AnalysisData VisualizationStatistical MethodologiesQuantitative Decision-MakingRegulatory ComplianceStatistical CommunicationsData IntegrityHealth Authority Standards
Soft Skills
Credo-Based LeadershipStrong Communication SkillsMentoring Emerging LeadersCollaborationProblem-Solving
Tools & Technologies
RSASComputational ToolsInteractive Graphical ToolsArtificial Intelligence
Industry Keywords
Pharmaceutical Research And DevelopmentTherapeutic AreasGxP ActivitiesClinical Data AnalysisCross-Pharma Consortia

About the role

Key responsibilities & impact
  • Lead major portions of biostatistical research and development projects independently
  • Apply advanced statistical expertise to experimental design, modeling, analysis planning and execution, interpretation, and statistical communications
  • Analyze and visualize study, experiment, or trial data
  • Identify and solve scientific, statistical, regulatory, operational, and partnership complexities
  • Lead innovative statistical methodologies and business process improvements
  • Guide study and trial design optimization
  • Support strategic scenario planning, quantitative decision-making, and regulatory activities
  • Collaborate cross-functionally to identify and resolve issues
  • Serve as point of contact for project or program deliverables
  • Represent Statistics & Decision Sciences on development teams, working groups, senior management reviews, and health authority interactions
  • Build partnerships with internal colleagues, CROs, consultants, and other external partners
  • Drive statistical methodology advancement through scholarly publications and presentations
  • Participate in professional organizations, cross-pharma consortia, and industry standards development
  • Author scientific journal manuscripts and peer review or edit professional journal manuscripts
  • Supervise contractors, special assignment personnel, interns, or co-ops as required
  • Mentor emerging leaders in techniques, processes, and responsibilities
  • Ensure quality, timeliness, compliance, and adherence to project and company standards

Requirements

What you’ll need
  • Master’s Degree in Statistics with 10+ years experience OR PhD in Statistics with 7+ years in related clinical data analysis experience
  • Credo-based leadership consistent with J&J IM Leadership Imperatives
  • Advanced data analytics expertise grounded in statistical principles
  • Full proficiency in R and SAS
  • Familiarity with computational tools, innovative data-adaptive methods, and artificial intelligence
  • Knowledge of statistical methodologies, drug development, pharmaceutical research and development, and health authority standards
  • Experience across multiple disease areas/targets within or across Therapeutic Areas
  • Strong written, oral, and interpersonal communication skills
  • Ability to translate intricate statistical concepts for non-statisticians
  • Proficiency communicating statistical findings using interactive graphical tools
  • Understanding of regulatory guidance, GxP activities, Data Integrity, and company standard operating procedures
  • Ability to supervise contractors, special assignment personnel, interns, or co-ops as required
  • Ability to mentor emerging leaders
  • Ability to comply with project and company standards and deliverables

Benefits

Comp & perks
  • Consolidated retirement plan (pension)
  • Savings plan (401(k))
  • Long-term incentive program
  • Vacation –120 hours per calendar year
  • Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year
  • Holiday pay, including Floating Holidays –13 days per calendar year
  • Work, Personal and Family Time - up to 40 hours per calendar year
  • Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
  • Bereavement Leave – 240 hours for an immediate family member; 40 hours for an extended family member per calendar year
  • Caregiver Leave – 80 hours in a 52-week rolling period
  • Volunteer Leave – 32 hours per calendar year
  • Military Spouse Time-Off – 80 hours per calendar year