AD, Medical Information, Established Product Communications

Johnson & JohnsonTitusville, NJ
Onsite

About The Position

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 MedTech, 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. Learn more at jnj.com As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. The Associate Director, Medical Information, Established Product Communications is responsible for leading the Medical Information support for Established Products (and investigational products, as requested), including development and maintenance of scientific responses. Leverages knowledge and expertise to provide medical guidance for promotional materials and develop scientific training. Partners closely with Established Products MAF for issue resolution, product changes and events. Collaborates with peers to develop consistent processes and communication. Contributes to Medical Information projects and initiatives.

Requirements

  • A minimum of a Bachelor’s degree in Pharmacy is required.
  • A minimum of 6 years of experience within a Medical Information function is required.
  • Demonstrated ability to conduct literature analysis and develop both scientific responses and slide decks to scientific inquiries from healthcare professionals is required.
  • Strong knowledge of Medical Information process, content management systems and technologies for scientific content required is required.
  • Experience with promotional material review is required.
  • Demonstrated success in innovation and creativity to cultivate new ideas and leverage solution to exceed customer needs is required.
  • Project management with product launch oversight experience is required.
  • Expertise working in a matrix environment with cross functional and cross-regional teams is required.

Nice To Haves

  • A PharmD or PhD degree is highly preferred.
  • Analysis of voice of customer data to identify unmet needs/data gaps is preferred.
  • Therapeutic area experience in cardiovascular, neuroscience, infectious disease, oncology, or pulmonary hypertension is preferred.

Responsibilities

  • Develop and maintain scientific responses – Leads the enhancement of medical information HCP scientific responses to optimize communication clarity and maintenance.
  • Provides oversight to medical writing vendor to author and maintain medical information scientific responses and innovative content in support of customer needs, including those from Payers and Health Systems (e.g. Medicaid formulary requests or other custom requests).
  • Leads the enhancement of medical information scientific responses to optimize communication clarity and maintenance.
  • Provides scientific consultation on escalation inquiries.
  • Disseminates updated labeling or product events to drug information publishers (i.e., compendia).
  • Assist with investigational product support as needed.
  • Partner with Medical Affairs – Collaborates to ensure firm understanding of product events and issues within established products (and investigational products, as requested).
  • Ensure any evolving information is incorporated into resources to allow for effective management of Medical Information requests.
  • Leverage knowledge and medical information expertise in promotional material review – Utilizes product and disease state knowledge to provide medical guidance for promotional material review to ensure accurate and balanced content is created for customers.
  • Develop scientific training materials – Develops and maintains departmental training for established products to ensure all individuals are prepared to expertly manage medical information inquiries.
  • Partner with label working group to understand the continuous evolution of product labels.
  • Lead and contribute to Medical Information projects and initiatives

Benefits

  • Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance.
  • 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)).
  • 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 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 Condolence Leave – 30 days for an immediate family member: 5 days for an extended family member Caregiver Leave – 10 days Volunteer Leave – 4 days Military Spouse Time-Off – 80 hours
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