Johnson & Johnson

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

Johnson & Johnson • $137K — $235K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Advanced Degree (PharmD or PhD) required
  • Minimum 6 years in Medical Information or Health Economics and Outcomes Research
  • Experience with NCCN and Clinical Pathway policies
  • Strong knowledge of medical writing and clinical response creation
  • Expertise in healthcare industry across multiple therapeutic areas
  • Excellent leadership and communication skills
  • Preferred experience with Health Technology Assessment (HTAs) organizations

Responsibilities

  • Lead development of tailored scientific materials for oncology products
  • Oversee AMCP approved products and Medicaid formulary requests
  • Collaborate on Payer Digital Assets with Med Info CSI-Digital partners
  • Ensure scientific accuracy in third-party information and AI outputs
  • Guide responses to unsolicited Medical Information Requests from Payers
  • Develop scientific information for Clinical Decision Resource Organizations
  • Serve as medical reviewer for oncology assets

Benefits

  • 401(k) and pension plan participation
  • 120 hours of vacation per year
  • 40 hours of sick time per year
  • 13 days of holiday pay annually
  • Parental leave of 480 hours
  • Volunteer leave of 32 hours per year
  • Caregiver leave of 80 hours in a rolling 52-week period
Full Job Description
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 a 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.


Education: Describe the minimum knowledge or educational requirements for the position. Include any degrees or certifications which are required and/or desirable.
  • Advanced Degree PharmD or PhD is required


Related experience: Describe the types of experience and typical number of years required for this role:
  • A minimum of 6 years of relevant experience in Medical Information or Health Economics and Outcomes Research is required
  • Experience in National Comprehensive Cancer Network (NCCN) and Clinical Pathway policies, submission, and manufacturers engagement process is required.
  • Strong knowledge of Medical Information process, medical writing, clinical response creation experiences are required
  • Expertise in the healthcare industry, clinical knowledge or practice across multiple therapeutic areas is required.
  • Excellence in leadership skills, collaboration in a matrix environment, influencing and communication (both written and presentation) are required
  • Experience with product value assessment by Health Technology Assessment (HTAs) Organization is preferred
  • Working knowledge of United States health care systems and payers - specifically understanding business models and perspectives of managed care and public sector - is preferred.
  • Customer Focus - drives excellent customer service and exhibits understanding of healthcare landscape


Other

This position based in Titusville, NJ and may require up to 10% domestic travel for conference attendance and company meetings.

Required Skills:

Preferred Skills:
Business Writing, Clinical Research and Regulations, Clinical Trials Operations, Coaching, Collaboration, Copy Editing, Data Synthesis, Industry Analysis, Medical Affairs, Medical Communications, Organizing, Proofreading, Quality Validation, Standard Operating Procedure (SOP), Tactical Planning, Technical Credibility

The anticipated base pay range for this position is :
$137,000.00 - $235,750.00

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

About Johnson & Johnson

Scio Diamond creates single-crystal Type IIa diamonds for the jewelry market and for industrial applications. It employs a patent-protected chemical vapor deposition (CVD) process in a precisely controlled laboratory setting to produce diamonds. It was founded in 2009 and is headquartered in Greenville, South Carolina.

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Learn more about Johnson & Johnson
Size
141,700 employees
Market Cap
$462.7 billion
Industry
Net Income
$14.7 billion
Founded
1886
5 Year Trend
+5.5%
Revenue
$82.5 billion
NASDAQ

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