Director, Global Real World Evidence
Johnson & Johnson
2 months ago
Remote friendly (Raritan, NJ)
United States
Clinical Research and Development
Director, Global Real-World Evidence (RWE)
You Will Be Responsible For:
- Lead global RWE strategy and execution for key immunology assets, including defining research questions, developing study protocols, designing study methodology, selecting/analyzing real-world data, and disseminating results to support medical adoption and product differentiation across regions.
- Serve as the GRWE representative on cross-functional franchise teams; partner with Global Medical Affairs and Market Access; act as RWE subject matter expert in the Global Integrated Evidence Generation Plan (IEG) and oversee global real-world data/evidence generation strategies.
- Advance RWE capabilities and best practices by sharing current RWE guidance, delivering technical training, strengthening internal expertise in advanced RWE methods, and supporting governance, quality standards, and compliance.
- Lead Evidence Lab coordination to drive concept development, stakeholder alignment, and prioritization of RWE opportunities within the Global IEGP process.
- Ensure compliance with regulatory, legal, and commercial regulations related to research conduct, data usage, and scientific communication.
Qualifications / Requirements:
- Master’s degree in a quantitative field (e.g., epidemiology, biostatistics, HEOR, pharmacoepidemiology); PhD preferred.
- Minimum 6 years of relevant experience in pharma, biotech, or healthcare consulting.
- Demonstrated expertise in observational research (prospective/retrospective) across study design, conduct, analysis, and reporting.
- Experience executing RWE studies using diverse real-world data sources; multi-country experience preferred.
- Understanding of global healthcare delivery, reimbursement, and payer dynamics desirable.
- Strong communication/storytelling/presentation skills; ability to translate complex methods and statistics for technical and non-technical stakeholders.
- Motivated, intellectually curious, and able to manage multiple priorities in a fast-paced environment.
- Proven experience in a matrixed, cross-functional environment.
- Proficiency in Word, Excel, PowerPoint; familiarity with SAS, R, Python.
Preferred Qualifications:
- Immunology therapy area experience.
- Programming experience with major statistical analysis systems.
- Knowledge of evidence-based medicine and comparative effectiveness analyses.
- Experience managing analytical/statistical activities with external service providers.
Other:
- Based in Raritan, NJ; up to 15% travel required.
You Will Be Responsible For:
- Lead global RWE strategy and execution for key immunology assets, including defining research questions, developing study protocols, designing study methodology, selecting/analyzing real-world data, and disseminating results to support medical adoption and product differentiation across regions.
- Serve as the GRWE representative on cross-functional franchise teams; partner with Global Medical Affairs and Market Access; act as RWE subject matter expert in the Global Integrated Evidence Generation Plan (IEG) and oversee global real-world data/evidence generation strategies.
- Advance RWE capabilities and best practices by sharing current RWE guidance, delivering technical training, strengthening internal expertise in advanced RWE methods, and supporting governance, quality standards, and compliance.
- Lead Evidence Lab coordination to drive concept development, stakeholder alignment, and prioritization of RWE opportunities within the Global IEGP process.
- Ensure compliance with regulatory, legal, and commercial regulations related to research conduct, data usage, and scientific communication.
Qualifications / Requirements:
- Master’s degree in a quantitative field (e.g., epidemiology, biostatistics, HEOR, pharmacoepidemiology); PhD preferred.
- Minimum 6 years of relevant experience in pharma, biotech, or healthcare consulting.
- Demonstrated expertise in observational research (prospective/retrospective) across study design, conduct, analysis, and reporting.
- Experience executing RWE studies using diverse real-world data sources; multi-country experience preferred.
- Understanding of global healthcare delivery, reimbursement, and payer dynamics desirable.
- Strong communication/storytelling/presentation skills; ability to translate complex methods and statistics for technical and non-technical stakeholders.
- Motivated, intellectually curious, and able to manage multiple priorities in a fast-paced environment.
- Proven experience in a matrixed, cross-functional environment.
- Proficiency in Word, Excel, PowerPoint; familiarity with SAS, R, Python.
Preferred Qualifications:
- Immunology therapy area experience.
- Programming experience with major statistical analysis systems.
- Knowledge of evidence-based medicine and comparative effectiveness analyses.
- Experience managing analytical/statistical activities with external service providers.
Other:
- Based in Raritan, NJ; up to 15% travel required.