Janssen Global Services, LLC, a member of Johnson & Johnson's Family of Companies, is recruiting for an Associate Director, Patient Reported Outcomes (PRO) to be located in Raritan, NJ or Horsham, PA. (2 positions)
At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are working to create a world without disease. Transforming lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us. We bring together the best minds and pursue the most promising science. We are Janssen. We collaborate with the world for the health of everyone in it. Learn more at and follow us @JanssenGlobal. Janssen Global Services, LLC is part of the Janssen Pharmaceutical Companies.
Janssen Global Services, LLC encompasses groups that provide leadership across critical business areas for Janssen including, Global Commercial Strategy Organization; Global Pharmaceuticals Communication and Public Affairs; U.S. Pharmaceuticals Procurement Group; and Pharmaceuticals Group Business Development
The Associate Director, Patient Reported Outcomes (PRO) works closely with the PRO team to facilitate PRO-related activities in support of studies conducted for products in development in the Janssen R&D organization. The PRO Associate Director is responsible for managing PRO-related activities for assigned compounds in development, as well as for providing scientific expertise in measurement and psychometric analytic issues across therapeutic areas. The PRO Associate Director may be responsible for leading the PRO program and be responsible for all PRO-related aspects for a compound. The PRO Associate Director provides background information on competitor drug PRO research, conducts PRO literature searches, conducts qualitative research, works with the clinical team to incorporate PRO instruments into clinical studies, oversees analyses and publications, and generally represents the PRO function in clinical trial working groups and other teams.
KEY RESPONSIBILITIES
Lead activities under the direction of a PRO Lead:
Provide clinical teams with the information necessary for the appropriate incorporation of PRO measures in clinical studies
Provide information and guidance in choosing appropriate PRO instruments for clinical studies
Sections of documentation and communication for regulatory agencies in support of submission activities
Abstracts and manuscripts presenting PRO results from clinical studies
Identify, evaluate and manage projects with researchers and PRO vendors external to the company, including but not limited to qualitative research, cultural validation studies, validation studies for special populations, and quantitative analyses
QUALIFICATIONS - A Master’s degree or PhD in the field of psychology, psychometrics, sociology, health economics, biostatistics, epidemiology, public health or health services research, or PharmD. - A minimum of 4 or more years of Patient Reported Outcomes experience is required.
The base pay range for this position is MIN $131,000 to MID $196,000
At Johnson & Johnson, we’re on a mission to change the trajectory of health for humanity. That starts by creating the world’s healthiest workforce. Through cutting-edge programs and policies, we empower the physical, mental, emotional, and financial health of our employees and the ones they love. As such, candidates offered employment must show proof of COVID-19 vaccination or secure an approved accommodation prior to the commencement of employment to support the well-being of our employees, their families and the communities in which we live and work.
For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit
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.
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