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Associate Director, Real World Value and Evidence, Pulmonary Hypertension
Company: Johnson & Johnson
Location: Titusville, NJ
Employment Type: Full Time
Date Posted: 05/22/2021
Expire Date: 12/08/2021
Job Categories: Advertising/Marketing/Public Relations, Biotechnology and Pharmaceutical, Finance/Economics, Government and Policy, Healthcare, Other, Healthcare, Practitioner and Technician, Information Technology, Legal, Sales, Franchising, Research & Development, Medical, Writing/Authoring
Job Description
Associate Director, Real World Value and Evidence, Pulmonary Hypertension

Janssen Scientific Affairs, a member of Johnson & Johnson’s Family of Companies, is recruiting for an Associate Director, Real World Value and Evidence, Pulmonary Hypertension to be located in Titusville, NJ. 


At the Janssen Pharmaceutical Companies of Johnson & Johnson, what matters most is helping people live full and healthy lives. We focus on treating, curing and preventing some of the most devastating and complex diseases of our time. And we pursue the most promising science, wherever it might be found. 


Janssen Scientific Affairs, LLC is dedicated to providing medical information and consultative support to the Janssen pharmaceutical companies.


We are Janssen. Our mission drives us. Our patients inspire us. We collaborate with the world for the health of everyone in it.


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 Real World Value & Evidence (RWV&E) organization must ensure we obtain robust payer insights, deliver unrivaled value evidence, be patient-centric, execute timely real world data analytics, and develop flawless and impactful communication of the value of Janssen’s innovations for payers and society.


In this position, the Associate Director, Real World Value and Evidence, Pulmonary Hypertension will be responsible for building in collaboration with cross-functional teams the market access scientific strategy, evidence generation, and dissemination plans for a legacy Actelion product and/or above brand responsibilities to support the franchise.   Key responsibilities are as follows:


  • Ensure that real world evidence and market access scientific support requirements are understood and built-in to the US business plans
  • Develop and refine key research questions, prioritize research requirements, in collaboration with the RWVE therapeutic area lead and integrated evidence teams, and partner with RWV&E FIELD.
  • Collaborate with internal and external experts to prioritize and generate rigorous scientific data
  • Design, conduct, and manage studies, manage publications, and develop or update communication materials (e.g., Evidence & Access decks)
  • Ensure compliance with regulatory, legal and commercial in conducting research and dissemination of scientific information
  • Serve as subject matter, and functional area expert in responding to U.S-focused Health Technology/Value Assessments of our products by external organizations
  • Represent RWV&E on assigned cross-functional franchise teams, with internal partners such as RWVE colleagues, Marketing, Medical Affairs, Strategic Customer Group, GCSO, Epidemiology, Government Affairs and Policy, other J&J Operating Companies as needed.



  • 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:



  • A minimum of 6 years of relevant research experience.
  • Solid experience in conducting Real World Evidence studies applying health economics, patient-reported outcomes, retrospective data analyses, epidemiology or health services research.
  • Experience 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 collaboration, influencing and communication (both written and presentation) skills.
  • Experience in communicating technical data both internally and externally to non-technical audiences.
  • Independent high- level planning and execution of research strategies.
  • 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.
  • Proven medical writing skills (published papers, posters, and abstracts)
  • 20% travel required mostly national with occasional international travel.




  • Demonstrates innovative / creative approaches to identify and assess new research methodologies and opportunities to develop outcomes research projects.
  • Behaves with honesty and integrity and in the spirit of J&J’s Credo
  • Attains business results / goals and objectives
  • Creates value for customers
  • Thinks strategically in project implementation
  • Builds interdependent partnering
  • Implements positive change


 Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.


Primary Location
United States-New Jersey-Titusville-1125 Trenton Harbourton Road
Janssen Scientific Affairs, LLC (6120)
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