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Director, R&D Data Science & Digital Health, Real-World Evidence (RWE), Across Therapeutic Areas

Johnson & Johnson
Full-time
Remote friendly (Spring House, PA)
United States
$160,000 - $276,000 USD yearly
Clinical Research and Development

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Role Summary

Director, R&D Data Science & Digital Health, Real-World Evidence (RWE), Across Therapeutic Areas. Flexible primary location (Titusville, NJ; Raritan, NJ; Spring House, PA; Cambridge, MA; or San Diego, CA).

Responsibilities

  • Lead cross-TA RWE initiatives that support clinical development, regulatory submissions, and strategic decision-making.
  • Partner with internal stakeholders and external collaborators to co-create integrated RWE strategies and solutions.
  • Contribute to shaping regulatory policy and standards for RWE through scientific engagements.
  • Develop and disseminate best practices for novel RWE design and methodologies.
  • Provide scientific leadership and subject matter expertise in study design, analytics, and interpretation of evidence research.
  • Support the development of internal capabilities and tools to accelerate evidence generation and delivery.
  • Promote a culture of innovation, scientific rigor, and continuous learning across the RWE function.

Qualifications

  • Required: Ph.D. or Masterโ€šร„รดs in epidemiology, biostatistics, outcomes research, health policy, or related field.
  • Required: 8+ years of relevant experience in biopharma, RWE consulting, or healthcare industries.
  • Required: 3+ years of experience as a people manager.
  • Required: Proven expertise in data extraction, cleaning, and analysis; strong grasp of advanced statistical methods.
  • Required: Experience with diverse data sources (EHR, claims, registries, trial data, digital health).
  • Required: Strong communication skills to engage technical and non-technical stakeholders.
  • Required: Leadership and influencing capabilities with cross-functional alignment track record.
  • Required: Highly motivated, intellectually curious, with executional rigor.
  • Required: Proficiency in R, Python, or SQL.
  • Preferred: Experience in regulatory-grade evidence generation and regulatory engagement.
  • Preferred: Ability to lead cross-functional initiatives and influence without authority.
  • Preferred: Subject matter expertise in one or more therapeutic areas.
  • Preferred: Experience in matrixed, global organizations.

Skills

  • Advanced Analytics
  • Budget Management
  • Compliance Management
  • Critical Thinking
  • Data Analysis
  • Data Privacy Standards
  • Data Quality
  • Data Reporting
  • Data Savvy
  • Data Science
  • Data Visualization
  • Developing Others
  • Digital Fluency
  • Inclusive Leadership
  • Leadership
  • Program Management
  • Strategic Thinking
  • Succession Planning

Education

  • Ph.D. or Masterโ€šร„รดs in epidemiology, biostatistics, outcomes research, health policy, or related field.

Additional Requirements

  • None beyond those specified above.
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