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Director, Global Medical Affairs Strategy and Execution, Specialty Ophthalmology

Company: Disability Solutions
Location: Raritan
Posted on: June 1, 2024

Job Description:

Johnson and Johnson Family is recruiting a Director, Strategy and Execution, Specialty Ophthalmology located in Raritan, NJ. 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 The Director, Strategy and Execution is responsible for managing and supporting the Inherited Retinal disease (IRD) therapeutic area within the J&J Innovative Medicine Specialty Ophthalmology Global Medical Affair team. This individual will lead the development, planning and execution of several Global Medical Affairs (GMAF) data generation and dissemination strategies and projects, as outlined below: The Director, Global Medical Affairs Strategy and Execution will be responsible for:

  • GMAF Strategic Plans - co-development of a consolidated global Medical Affairs Strategy (MAS) that meets prioritized global and regional strategic imperatives; providing expert knowledge in the MAS planning process; driving the creation of final MAS.
  • Worldwide Integrated Evidence Generation Plan (WWIEGP) - lead the WWIEGP process; provides strategic input; consolidation of cross-functional and regional inputs and ensures successful and timely completion of the WWIEGP
  • Global Publication Plan - good understanding of our clinical data and clinical development program; provides strategic input to the data dissemination plan and ensures execution of the publication plan; ensure that the development of publications compliant to publication policies and SOPs: coordinate publication discussions with internal stakeholders (i.e. R&D, market access, regions, etc.) and publication agency partners.
  • Global Congress Strategy and Planning - lead scientific and strategic planning to support the overall global congress plan; coordinate and collaborate with cross-functional teams and key colleagues to align on medical affairs booth strategy and congress content development; manage/lead internal congress engagement/communications.
  • External Engagement - work closely with the GMAF team to execute external engagement meetings such as advisory boards, scientific advisory councils, steering committees. Includes things such as assist with content development/review of materials, meeting management, HCP engagements, HCP contract management, post-meeting follow-ups.
  • Global Scientific Communications - develop and disseminate accurate, timely and compliant scientific content (i.e. Scientific Communications Platform, Core Slide Decks) that meets the needs of internal and external stakeholders.
  • GMAF Business Plan - Lead through the IRD business planning process, including the development of the global medical affairs plan, associated tactics and budget.
  • GMAF Budget Oversight and Forecasting - manage/provide oversight for the GMAF budget for the IRD area.
  • GMAF Team Meetings management - leading, coordinating and actively participating in cross-functional strategy meetings, ad-hoc CDT meetings, global and regional discussions, and scientific knowledge exchange forums.
  • Oversight of GMAF SharePoint Site content and Scientific and knowledge Information Management (SKIM) platform for the IRD area.
  • Managing scientific agency relationships and interactions. Ensure optimal project and vendor management in the execution of GMAF strategies and tactics; develop sourcing strategies and effective partnerships with vendors/agencies and other key external partners.
  • IIS/Pre-Approval Access -oversight and intake and Global Review Committee Review, if applicable. Coordinate with cross functional team members and regions to track submissions, approvals, progress and budget for ongoing studies.
  • Provides expertise and oversight to ensure compliance with Cross-Pharma Policies and SOPs, Healthcare compliance and J&J Systems (i.e., JPUBs, ReCAP)

Keywords: Disability Solutions, New Brunswick , Director, Global Medical Affairs Strategy and Execution, Specialty Ophthalmology, Executive , Raritan, New Jersey

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