Job Function: Market Access
Job Sub Function: Health Economics Outcomes Research
Job Category:People Leader
All Job Posting Locations:Titusville, New Jersey, United States of America
Job Description:Director, Real World Value & Evidence - MilvexianWe are searching for the best talent for Director, Real World Value & Evidence - Milvexian, to be located within the Scientific Affairs US Team in Titusville, NJ.In the current environment of U.S. healthcare with a prominent focus placed on efficiency and affordability, ensuring patient access to innovative treatments is of utmost importance, but increasingly challenging. In this challenging environment, the Medical Affairs Real-World Value & Evidence organization must ensure we obtain robust payer insights, deliver unrivaled value evidence, be payer-centric, execute timely real world data analytics, and develop flawless and impactful communication of the value of Johnson & Johnson Innovative Medicine's contributions to payers and society.
Purpose: This role will report to the Therapeutic Area Lead Milvexian and is a member of the Milvexian Medical Affairs Team.
In this position, the Director, Real World Value & Evidence (RWV&E) will be responsible for leading lifecycle medical adoption and market access scientific strategies, evidence generation, and dissemination plans for Milvexian including multiple indications.
You will be responsible for:- Ensure real world evidence generation strategy 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 RWE activities to enable medical adoption and market access.
- RWE activities this role is held accountable for include but are not limited to: formulating key research questions addressing key stakeholder needs, identifying key analytical questions to shape market access strategy, designing and conducting studies, planning and conducting market access analytics, managing publications, developing communication materials for external stakeholders (e.g., Evidence & Access decks) and internal stakeholders demonstrating impact, and partnering with internal stakeholders such as V&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 medical adoption and 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 RWE studies, and models and/or tools developed to support the product.
- Serve as a leader on assigned cross-functional franchise teams, with internal partners such as RWE colleagues, Marketing, Medical Affairs, Strategic Customer Group, Global Commercial Strategy Organization, Epidemiology, Government Affairs and Policy, other J&J Operating Companies as needed.
Qualifications / Requirements:Education:
- 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.
Experience and skills:
Required:
- A minimum of 6 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 20% travel required mostly national with occasional international travel.
Preferred:
- 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.
- Experience with cardiovascular or anticoagulation disease area research
- Experience with population health or implementation science.
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Required Skills:Preferred Skills:Analytical Reasoning, Clinical Research and Regulations, Clinical Trials Operations, Communication, Consulting, Developing Others, Healthcare Trends, Health Outcomes Research, Inclusive Leadership, Leadership, Market Access, Market Access Strategies, Medical Affairs, Medical Communications, Medical Compliance, Outcomes Analysis, Outcomes Research, Product Strategies, Real World Data, Real World Evidence (RWE), Representing, Research Analysis, Research Proposals, Stakeholder Management, Strategic Thinking
The anticipated base pay range for this position is :$164,000.00 - $282,900.00
Additional Description for Pay Transparency:
Subject to the terms of their respective plans, employees are eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)).
This position is eligible to participate in the Company's long-term incentive program.
Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits:
Vacation -120 hours per calendar year
Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado -48 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
Bereavement Leave - 240 hours for an immediate family member: 40 hours for an extended family member per calendar year
Caregiver Leave - 80 hours in a 52-week rolling period10 days
Volunteer Leave - 32 hours per calendar year
Military Spouse Time-Off - 80 hours per calendar year
For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits
