Global Medical Affairs Leader, Director- Dermatology

Company: Disability Solutions
Location: Horsham
Posted on: February 1, 2025

Job Description:

Johnson & Johnson is recruiting for a Global Medical Affairs Leader (GMAL), Director- Dermatology in our Immunology Global Medical Affairs organization located in Horsham, Pennsylvania.\rAt 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 https://www.jnj.com/. \r\rFor more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.We know that the success of our business - and our ability to deliver meaningful solutions - depends on how well we understand and meet the diverse needs of the communities we serve. Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential. At Johnson & Johnson, we all belong.\r\rThe Global Medical Affairs Leader (GMAL), Director, Dermatology, under the direction of the Vice President of Global Medical Affairs for Dermatology/Rheumatology, is responsible for leading the clinical-commercial optimization of product development and life cycle management strategies and plans for the assigned compounds in clinical development for atopic dermatitis within the Immunology Therapeutic Area (TA). The GMAL will lead the Global Medical Affairs Team and partner closely with Regional Medical TA/product leaders to develop integrated Global Medical Affairs perspectives, strategies and plans for specified products, assets, and projects. The GMAL, will be a member of the Compound Development Teams (CDTs), the Safety Management Teams and Global Commercial Teams, as well as an ad hoc member of the Clinical Team and Global Market Access Team. The GMAL will be responsible for development of Global Medical Affairs plans that reflects prioritized regional needs and are included in the overall asset development plans. In addition, the GMAL will be accountable for the global publications plans, global opinion leader relations, global medical education (including symposia, speaker training) and global advisory boards for assets starting in early development (phase IIA) and through launch of major life cycle management initiatives (earlier or later as needed). The GMAL will also be responsible for facilitating and ensuring a consistent approach to Medical Affairs programs/activities globally.\rKey Responsibilities:

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• Develop Global Medical Affairs strategy and plan for the assigned compounds based on prioritized regional needs.
• Working with the CDT ensures integration with the overall global compound strategy, resulting in one global R&D and Medical Affairs compound development plan, inclusive of developing a Target Product Profile representing Medical Affairs global and regional value needs.
• Provide a single Medical Affairs voice into the creation of compound development and LCM strategies, plans and trial design from phase IIa through phase IV.
• Be responsible for pre-launch Medical Affairs activities including product/TA global advisory boards, medical symposia and congress activities, and coordination of regional activity in these areas.
• Be an active member of the CDT and lead a Global Medical Affairs Team consisting of regionally designated TA Medical Affairs Leaders to create one Medical Affairs perspective and one "unified" voice on the CDT.
• Collaborate closely with the regional Medical Affairs representatives to develop integrated Global Medical Affairs strategies and plans and maintain open, two-way communication to ensure regional Medical Affairs partners are up to date on all plans, progress and decisions.
• Synchronize input and output of the Medical Affairs plan with the strategic and business plan calendars.
• Maintain responsibility for the development and execution of global publication plans as well as review and approval of publications for marketed products and specified compounds in clinical development.
• Lead the ReCAP process (review of all Medical Affairs sponsored clinical trials and Investigator Initiated Sponsored studies) for applicable products.
• Support development of the Company risk management strategy and plan as well as author and review specific sections of the Periodic benefit-risk assessment report for compounds. Perform medical impact assessments as required.
• Maintain responsibility for ensuring that all global activities follow J&J Compliance principles (e.g. Health Care Compliance etc.)\r\r

Keywords: Disability Solutions, East Orange , Global Medical Affairs Leader, Director- Dermatology, Healthcare , Horsham, New Jersey