Associate Director, Real World Value and Evidence – Hematology

Johnson & Johnson • Horsham, PA

1d • Hybrid

About The Position

The Associate Director, Real World Value & Evidence (RWV&E) – Hematology will lead real-world evidence generation and outcomes research for assigned therapeutic areas and marketed products within J&J Hematology. This role combines technical expertise, strategic thinking, and cross-functional collaboration to support market access, payer value propositions, and healthcare provider education. You will be responsible for: Evidence Generation & Dissemination Conduct real-world evidence and outcomes research studies; create economic models for assigned therapeutic areas and products within J&J Hematology, under the guidance of the Director/Group Director. Lead the design, execution, and publication of evidence studies, outcomes research, and economic models in compliance with scientific standards, regulations, and J&J SOPs. Develop and update research and publication plans to support the Integrated Evidence Generation Plan (IEGP). Collaborate with internal and external experts to generate and disseminate robust scientific evidence, and contribute to development of dissemination plans, as aligned with the Integrated Evidence Team (IET), to support the RWV&E strategic plans for the assigned therapeutic areas. Collaborate with cross-functional teams to advance evidence generation and product market access. Manage research studies, market access analytics & activities and other related projects, as aligned with the IET and for other business needs Apply technical and strategic expertise to deliver evidence-based solutions supporting HCP education, market access strategies, and payer value propositions. Develop a deep understanding of US payer needs and integrate insights into payer communication materials. Champion the approval of new presentation materials and handle administrative responsibilities as needed. Ensure quality of design, execution, and publication of real-world evidence studies, and quality of models & tools developed for business partners Contribute to execution for RWV&E activities and market access supporting activities such as shaping of payer communication materials to support market access scientific strategies and payer value propositions in assigned areas of responsibility. Ensures compliance with regulatory, legal and commercial regulations (for example Contract Pricing Committee, Copy Approval Committee) in conducting research and dissemination of scientific information Project & Team Leadership Oversee research projects, analytics, and related activities from concept development to publication and pull-through in field materials. Manage project budgets, compliance reporting, and share learnings within the team. Represent RWV&E on cross-functional teams with business partners (e.g., Real World Analytics, Marketing, Medical Affairs, Strategic Customer Group, Global Commercial Strategy, Epidemiology, Government Affairs, New Business Development). Foster a collaborative, positive, and engaging work environment.

Requirements

• Master’s degree in health economics and outcomes research, pharmacoepidemiology, health services research, health policy, pharmacy, or related field required.
• Minimum 5+ years of experience in the pharma or healthcare industry, preferably in health economics, epidemiology, real-world evidence generation, outcomes research, or related functions.
• Fellowship experience may be considered.
• Strong foundation in two or more of: outcomes research, epidemiology, biostatistics, economic modeling.
• Experience executing projects from concept development through publication and pull-through in field materials with minimal oversight.
• Strong communication and presentation skills for technical and non-technical audiences.
• Strong project management skills; ability to drive solutions with agility and efficiency.
• Knowledge of US healthcare system, reimbursement, payor dynamics, pathways, and oncology care models desirable.
• Experience working in a matrix team environment required.
• Demonstrated ability to work collaboratively, embrace new ideas, contribute to shared learning, and foster a positive work environment.

Nice To Haves

• Doctorate (PhD) preferred.
• Experience in supporting alliance partnerships preferred.

Responsibilities

• Conduct real-world evidence and outcomes research studies; create economic models for assigned therapeutic areas and products within J&J Hematology, under the guidance of the Director/Group Director.
• Lead the design, execution, and publication of evidence studies, outcomes research, and economic models in compliance with scientific standards, regulations, and J&J SOPs.
• Develop and update research and publication plans to support the Integrated Evidence Generation Plan (IEGP).
• Collaborate with internal and external experts to generate and disseminate robust scientific evidence, and contribute to development of dissemination plans, as aligned with the Integrated Evidence Team (IET), to support the RWV&E strategic plans for the assigned therapeutic areas.
• Collaborate with cross-functional teams to advance evidence generation and product market access.
• Manage research studies, market access analytics & activities and other related projects, as aligned with the IET and for other business needs
• Apply technical and strategic expertise to deliver evidence-based solutions supporting HCP education, market access strategies, and payer value propositions.
• Develop a deep understanding of US payer needs and integrate insights into payer communication materials.
• Champion the approval of new presentation materials and handle administrative responsibilities as needed.
• Ensure quality of design, execution, and publication of real-world evidence studies, and quality of models & tools developed for business partners
• Contribute to execution for RWV&E activities and market access supporting activities such as shaping of payer communication materials to support market access scientific strategies and payer value propositions in assigned areas of responsibility.
• Ensures compliance with regulatory, legal and commercial regulations (for example Contract Pricing Committee, Copy Approval Committee) in conducting research and dissemination of scientific information
• Oversee research projects, analytics, and related activities from concept development to publication and pull-through in field materials.
• Manage project budgets, compliance reporting, and share learnings within the team.
• Represent RWV&E on cross-functional teams with business partners (e.g., Real World Analytics, Marketing, Medical Affairs, Strategic Customer Group, Global Commercial Strategy, Epidemiology, Government Affairs, New Business Development).
• Foster a collaborative, positive, and engaging work environment.

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 period
• 10 days Volunteer Leave – 32 hours per calendar year
• Military Spouse Time-Off – 80 hours per calendar year

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level