Johnson & Johnson logo

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

Johnson & Johnson
Remote friendly (Raritan, NJ)
United States
$173,000 - $299,000 USD yearly
Clinical Research and Development

Role Summary

Senior Director, R&D Data Science & Digital Health, Real-World Evidence (RWE), Across Therapeutic Areas. Lead RWE strategy and execution across therapeutic areas, shaping the future of RWE at the organization, driving collaborations, advancing regulatory-grade evidence generation, and elevating scientific leadership.

Responsibilities

  • Strategic Leadership & Ecosystem Building: Define and execute RWE initiatives across therapeutic areas, align with long-term goals, lead cross-functional RWE committees, and foster partnerships with internal and external stakeholders; shape the enterprise-wide RWE ecosystem through innovation, governance, and capability building.
  • Regulatory Policy & Scientific Influence: Serve as a strategic advisor on regulatory-grade evidence generation and policy shaping; lead preparation and presentation of scientific data packages for regulatory submissions and agency interactions; represent J&J in external forums to influence RWE standards and regulatory expectations.
  • Scientific Leadership & Methodological Excellence: Chair the Methodology Review Board (MRB); oversee a portfolio of high-impact RWE projects; establish best practices for novel study designs and implementation; promote continuous learning and innovation in emerging RWE methodologies and technologies; develop frameworks and tools to scale evidence generation and accelerate delivery; champion a culture of scientific rigor, collaboration, and execution excellence.

Qualifications

  • Required: Ph.D. or Master’s in epidemiology, biostatistics, outcomes research, health policy, or related field.
  • Required: 10+ years of relevant experience in biopharma, RWE consulting, or healthcare industries.
  • Required: 7+ 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, with the ability to effectively engage both technical and non-technical stakeholders.
  • Required: Proven leadership and influencing capabilities, with a track record of inspiring teams and driving cross-functional alignment.
  • Required: Highly motivated and intellectually curious, with strong executional rigor and a passion for solving complex challenges.
  • Required: Proficiency in R, Python, or SQL.
  • Preferred: Expertise in regulatory-grade evidence generation and regulatory engagement.
  • Preferred: Strong leadership in cross-functional initiatives and ability to influence without authority.
  • Preferred: Subject matter expertise in Oncology, Immunology, Neuroscience.
  • Preferred: Experience in matrixed organizations and global stakeholder engagement.

Skills

  • Regulatory-grade evidence generation
  • Cross-functional leadership
  • Data science methods and statistical analysis
  • Stakeholder engagement
  • R, Python, SQL proficiency

Education

  • Ph.D. or Master's in epidemiology, biostatistics, outcomes research, health policy, or related field