Johnson & Johnson

Assoc Director, HEMA Analytics and RWE

Johnson & Johnson$120K — $150K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Master's or PhD in Epidemiology, Biostatistics, Health Services Research, Health Economics, or related field.
  • Deep knowledge of US healthcare delivery and insurance reimbursement structures.
  • Over 6 years of experience in RWE, outcomes research, or health analytics, preferably in orthopaedics.
  • Hands-on experience with claims databases and electronic health records.
  • Proficiency in statistical software (SAS, R, Python) and data visualization tools (Tableau, Power BI).
  • Strong study design skills in retrospective cohort and case-control methods.
  • Excellent communication skills for presenting complex data.

Responsibilities

  • Develop and maintain analytics infrastructure and reporting tools for decision-making.
  • Conduct advanced statistical analyses and burden-of-illness studies.
  • Design and execute real-world evidence studies using various secondary data sources.
  • Lead end-to-end study management including data acquisition and analysis.
  • Partner with stakeholders to align RWE projects with business objectives.
  • Manage relationships with external data vendors and academic collaborators.
  • Ensure compliance with regulatory standards and mentor junior analysts.

Benefits

  • Travel allowance up to 20%.
  • Hybrid work environment options.
Full Job Description
Job Function:
Market Access

Job Sub Function:
Health Economics Market Access

Job Category:
Professional

All Job Posting Locations:
Palm Beach Gardens, Florida, United States of America, Raritan, New Jersey, United States of America, Raynham, Massachusetts, United States of America, Warsaw, Indiana, United States of America, West Chester, Pennsylvania, United States of America

Job Description:

Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals. Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes.

Key Responsibilities

Advanced Analytics & Infrastructure
• Develop and maintain HEMA analytics infrastructure, dashboards, and reporting tools to support evidence-based decision-making across the organization
• Conduct advanced statistical analyses including comparative effectiveness, outcomes research, burden-of-illness studies, predictive modeling, and utilization and reimbursement analyses
• Build and maintain standardized analytic code libraries, data pipelines, and reproducible research workflows
• Evaluate and recommend new data sources, analytics platforms, and methodological approaches to strengthen the organization's RWE capabilities

Real-World Evidence Study Design & Execution
• Design and execute real-world evidence studies using claims and billing databases, registries, electronic health records, and other secondary data sources to support the Orthopaedics portfolio
• Lead end-to-end study management including protocol development, IRB/ethics submissions, data acquisition, analysis, reporting and manuscript drafting
• Apply rigorous epidemiological and biostatistical methods including retrospective cohort, case-control, interrupted time series, difference-in-differences, and propensity score matching approaches
• Develop and validate real-world endpoints and outcome measures relevant to orthopedic procedures and technologies

Evidence Strategy & Cross-Functional Partnership
• Partner with cross functional stakeholders to identify evidence gaps and prioritize RWE projects aligned with business objectives and product lifecycle needs
• Contribute to the development of integrated evidence plans that span clinical, economic, and humanistic outcomes across the portfolio
• Support payer and HTA submissions with robust RWE and analytics deliverables, including evidence dossiers, systematic literature reviews, and indirect treatment comparisons

External Collaboration & Scientific Communication
• Manage relationships with external data vendors, academic collaborators, and contract research organizations
• Author and contribute to peer-reviewed publications, congress presentations, white papers, and technical reports
• Translate complex analytical findings into clear, compelling narratives for diverse audiences including commercial, medical, and executive stakeholders
• Represent the organization at scientific conferences, advisory boards, and industry working groups

Compliance, Quality & Team Development
• Ensure all studies comply with relevant regulatory, ethical, and data privacy standards including HIPAA
• Maintain rigorous documentation standards and ensure reproducibility of all analyses
• Mentor junior analysts, participate in peer reviews and contribute to the development and strategic direction of the RWE and analytics function within HEMA

Qualifications
• Master's degree or PhD in Epidemiology, Biostatistics, Health Services Research, Health Economics, or related quantitative field
• Deep knowledge of US healthcare delivery systems, and public and private insurance reimbursement structures
• 6+ years of experience in RWE, outcomes research, or health analytics within the medical device, MedTech, or pharmaceutical industry; orthopaedics subject matter expertise (e.g., joint reconstruction, trauma, spine, sports medicine) preferred
• Hands-on experience with claims databases (e.g., Medicare, MarketScan, Optum), and electronic health records
• Proficiency in SAS, R, Python, or similar statistical software; SQL, and data visualization tools (e.g., Tableau, Power BI)
• Strong study design capabilities, including retrospective cohort, case-control, and quasi-experimental methods
• Excellent communication skills with the ability to present complex data to non-technical audiences; publication track record preferred
• Demonstrated ability to manage multiple projects simultaneously with competing deadlines

Other:

  • Travel up to 20%


#LI-Hybrid

#DePuySynthesCareers

Required Skills:

Preferred Skills:
Agility Jumps, Commercial Awareness, Competitive Landscape Analysis, Cross-Functional Collaboration, Customer Intelligence, Global Market, Go-to-Market Strategies, Health Economics, Health Intelligence, Market Knowledge, Market Opportunity Assessment, Mentorship, Organizing, Pricing Strategies, Regulatory Compliance, Strategic Change, Tactical Planning, Technical Credibility

About Johnson & Johnson

Scio Diamond creates single-crystal Type IIa diamonds for the jewelry market and for industrial applications. It employs a patent-protected chemical vapor deposition (CVD) process in a precisely controlled laboratory setting to produce diamonds. It was founded in 2009 and is headquartered in Greenville, South Carolina.

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Learn more about Johnson & Johnson
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141,700 employees
Market Cap
$462.7 billion
Industry
Net Income
$14.7 billion
Founded
1886
5 Year Trend
+5.5%
Revenue
$82.5 billion
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