Jobs · Pennsylvania

Senior Principal Scientist, Data Science RWE

Johnson & Johnson Innovative Medicine · Spring House, PA · 3 days ago
Hybrid$137k–$236k/yrFull-time

About the role

The Real-world Evidence & Advanced Analytics team within Johnson & Johnson Innovative Medicines is seeking a hands-on scientific and technical leader to join our team. This role includes:

  • Leading a portfolio of Real-World Evidence (RWE) projects
  • Developing best practices and mentoring team members
  • Identifying common technical requirements for RWE projects
  • Maintaining a common suite of tools for RWE data scientists
  • End-to-end expertise in RWE studies, including research question conceptualization, data feasibility, study design, analysis, programming, and interpretation
  • Providing thought leadership and hands-on programming expertise for RWD methodologies
  • Generating actionable insights from post-hoc RCT analyses, observational databases, and literature reviews
  • Partnership with Data Science Therapeutic Area scientists to conceptualize, lead, shape, and deliver RWE

Responsibilities

Key responsibilities include:

  • Hands-on scientific and technical leadership in RWE projects
  • Development and maintenance of a common suite of tools for RWE data scientists
  • End-to-end expertise in RWE studies
  • Programming expertise for RWD methodologies
  • Statistical analysis and programming deliverables creation
  • Interacting with regulatory agencies
  • Collaboration with Data Science Therapeutic Area scientists

Requirements

Qualifications required:

  • Ph.D. in epidemiology or biostatistics
  • Expert coding skills using R, Python, or SAS
  • At least 5 years of relevant experience in biopharma companies, RWE consulting firms, or healthcare industries
  • Extensive hands-on experience with data extraction, cleaning, and analysis, as well as statistical methods to mitigate confounding and selection biases
  • Expertise with multiple real-world data sources (EHR, insurance claims, registry data)
  • Familiarity with clinical trial data structure
  • Excellent interpersonal, communication, and presentation skills

Preferred Qualifications

  • Familiarity with drug discovery and clinical development processes
  • Subject matter knowledge in oncology, immunology, or neuroscience
  • Experience in regulatory-grade evidence and responding to agency reviews

Skills

  • Advanced analytics
  • Consulting
  • Critical thinking
  • Data analysis
  • Data privacy standards
  • Data quality
  • Data reporting
  • Data savvy
  • Data science
  • Data visualization
  • Digital fluency
  • Econometric models
  • Mentorship
  • Strategic thinking
  • Tactical planning
  • Technical credibility

Benefits

  • Pension plan
  • 401(k) savings plan
  • Long-term incentive program
  • Vacation
  • Sick time
  • Holiday pay
  • Parental leave
  • Bereavement leave
  • Caregiver leave
  • Volunteer leave
  • Military spouse time-off

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