Associate Director, Medical Information - Payer & Health Systems; ONC)

Position: Associate Director, Medical Information - Payer & Health Systems (ONC)
Location: Titusville

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and Med Tech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.

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Job Function:

Medical Affairs Group
Job Sub Function:

Medical Writing
Job Category:

Professional
All Job Posting Locations:

Titusville, New Jersey, United States of America
Job Description:

Johnson & Johnson is recruiting for an Associate Director, Medical Information, Payer and Health Systems to be located in Titusville, NJ. The Associate Director, Medical Information, Payer and Health Systems reports to the Director Med Info-PHS and leads the strategy for the development and dissemination of Medical Information scientific content and materials to Payers, Healthcare Intermediaries and Health Systems across the oncology portfolio of J&J IM products.

Responsible for quantitative and qualitative payer content related success criteria reports and metrics. Payer Scientific Content and Materials – 70% Leads the development and timely dissemination of tailored, evidence-based scientific materials for oncology products. Leads the development of AMCP approved products and pre-approval dossiers, Medicaid formulary requests, and custom requests working collaboratively with Medical Affairs and Real-World Value & Evidence (RW V&E) therapeutic area leads.

Engages in shaping and development of the Payer Digital Assets in collaboration with Med Info CSI-Digital partners. Leads the development and dissemination of scientific information to NCCN guidelines/compendia/clinical pathway developers Leads the correction of third-party information and AI generated outputs to ensure scientific accuracy, quality, compliance and alignment. Works closely with V&ESE Field, Medical Affairs Therapeutic Area team(s) to guide creation and delivery of responses to unsolicited Medical Information Requests from Payers and Health Systems Leads the development and dissemination of scientific information in support of assigned products to Clinical Decision Resource Organizations (CDRO) in partnership with Medical Affairs, RW V&E, SCG, Therapeutic Area Teams Serves as medical reviewer for SCG copy approval committee for oncology assets.

Support interactions with drug compendia and collaborates with Director Med Info PHS and business partners to evaluate strategies for compendia interactions. Ensures optimized delivery of high-quality and efficient Payer scientific content and materials by vendors, provides real-time feedback and first line scientific review of materials as needed. Voice of Customer and Metrics – 20% Leverage voice of customer and other sources of customer information and identify actionable items to enhance development of Payer and Health Systems materials.

Projects and Research – 10% Participates in ad-hoc projects and activities as assigned by management. Conducts benchmark and research on the landscape of Payer, Healthcare Intermediaries, and health systems.
Payer Scientific Content and Materials – 70%
• Leads the development and timely dissemination of tailored, evidence-based scientific materials for oncology products.
• Leads the development of AMCP approved products and pre-approval dossiers, Medicaid formulary requests, and custom requests working collaboratively with Medical Affairs and Real-World Value & Evidence (RW V&E) therapeutic area leads.
• Engages in shaping and development of the Payer Digital Assets in…