Johnson & Johnson Innovative Medicine · 1 day ago
Director, Real World Value and Evidence - IRA and Early Pipeline Products
Johnson & Johnson is a leader in healthcare innovation committed to improving health for humanity. The Director, Real World Value and Evidence will lead market access scientific strategy and evidence generation for early pipeline products, ensuring that the needs of key payer stakeholders are met through robust value evidence and timely analytics.
Pharmaceuticals
Responsibilities
Ensure real world evidence and market access scientific support requirements are understood and built-in to the US business plans with value propositions that reflect the needs of key payer stakeholders and lead scientific strategic planning for RWV&E activities to enable market access
RWV&E activities this role is held accountable for include but are not limited to: formulating key research questions, identifying key analytical questions to shape market access strategy, designing and conducting studies, planning and conducting market access analytics, managing publications, developing communication materials (e.g., Evidence & Access decks), and partnering with RWV&E Field to ensure effective and compliant communication to payer customers
Ensures projects are aligned to the Integrated Evidence Generation Plan (IEGP) and business needs and executed on time
Collaborate with internal and external experts to prioritize and generate rigorous scientific data, and develop dissemination plans to support the product’s IEGP
Ensures compliance with regulatory, legal and commercial regulations (for example Contract Pricing Committee, Copy Approval Committee) in conducting research and dissemination of scientific information
Collaborate with cross-functional business partners on scientific strategies to support market access for our products
Directly initiate and manage research studies and other related projects
Serve as subject matter, and functional area expert in responding to U.S-focused Health Technology/Value Assessments of our products by external organizations
Ensure quality of design, execution, and publication of real-world evidence studies, and quality of models & tools developed for business partners
Develop annual business plan budget, present to appropriate levels of management for approval, and manage budgeted funds appropriately
Ensure quality in internal / external communications including: publications, training support of RWVE studies, and models and/or tools developed to support the product
Qualification
Required
A minimum of a Master's degree in Public Health, Health Services Research, Economics, Epidemiology, Pharmacy, Health Policy, or a related discipline is required; a doctorate or other advanced degree is preferred
A minimum of 7 or more years of relevant research experience
Expertise in healthcare industry, clinical knowledge or practice across multiple therapeutic areas, medical reimbursement, technical expertise in economic evaluations or patient reported outcomes, including data analysis and statistics
Excellent in leadership skills, collaboration, influencing and communication (both written and presentation)
Serve as a leader on the assigned cross-functional franchise teams pertaining to observational data or research, market access scientific strategy, payer insights/ data needs, etc
Experience in communicating technical data both internally and externally to non-technical audiences
Independent high-level planning and execution of research strategies
Solid experience in conducting Real World Evidence studies applying health economics, patient-reported outcomes, retrospective data analyses, epidemiology or health services research
Firm understanding of drug development process including health economic inputs needed to support the value proposition
Firm understanding of regulatory standards for approval and communication of data
Firm understanding of United States health care systems and customers; specifically understanding unique business models and perspectives
Firm understanding of the uses of evidence-based medicine and comparative effectiveness analyses for health policy decision-making
Up to 30% travel required mostly national with occasional international travel
Experience in developing and gaining management approval for value-based scientific strategies and tactics to meet both commercial and scientific objectives for a given product or therapeutic area
Benefits
Medical
Dental
Vision
Life insurance
Short- and long-term disability
Business accident insurance
Group legal insurance
Consolidated retirement plan (pension)
Savings plan (401(k))
Long-term incentive program
Vacation –120 hours per calendar year
Sick time - 40 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year
Holiday pay, including Floating Holidays –13 days per calendar year
Work, Personal and Family Time - up to 40 hours per calendar year
Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
Condolence Leave – 30 days for an immediate family member: 5 days for an extended family member
Caregiver Leave – 10 days
Volunteer Leave – 4 days
Military Spouse Time-Off – 80 hours
Company
Johnson & Johnson Innovative Medicine
Johnson and Johnson Innovative Medicine focuses on developing medical solutions for some of the challenging diseases and medical conditions.
Funding
Current Stage
Late StageRecent News
2025-08-14
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