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Global Franchise Medical Director, Belamaf Oncology/Hematology

GSK
Job LocationPennsylvania, Exeter
EducationNot Mentioned
SalaryCompetitive salary
IndustryNot Mentioned
Functional AreaNot Mentioned
Job TypePermanent, full-time

Job Description

Site Name: Switzerland - Zug, UK - London - Brentford, USA - Pennsylvania - Upper Providence, USA - Pennsylvania - PhiladelphiaPosted Date: Jul 2 2020Are you familiar with the facts on BCMA / If you are inclined to want to join our journey to improve the lives of patients with Multiple Myeloma, then this is a career opportunity to explore. GSK Oncology R&D is focused on building industry-leading portfolios in four cutting-edge areas of science:

  • Immuno-Oncology: Invest to develop differentiated assets and combinations in increasingly crowded I-O space.
  • Cell/Gene Therapy (CGT): Utilize competitive platform play based on patented technology.
  • Cancer Epigenetics: Take a more focused approach, pruning some existing assets while maintaining efforts in discovery and clinical development of most promising programs.
  • Genetic Medicines: Inhibiting pathways that contribute to aberrant DNA repair.
    • Details about our portfolio can be found here: GSK 2018 Annual ReportGSK Product PipelineMEDICAL AFFAIRS at GSK:Our medical affairs physicians and scientists are the experts on our medicines/vaccines and an extremely valuable part of our global business. In all countries where our medicines and vaccines are marketed, these professionals help to ensure that healthcare professionals can understand the appropriate use of our products and ensure that the patient remains at the heart of our decision making. Our Global Medical organization, under the leadership of Sabine Luik, SVP-Global Medical & Regulatory Affairs and Chief Medical Officer, is at the forefront of the industry-leading changes to improve patient treatment options. We are committed to making GSK’s Medical Affairs team the best in our industry, and a trusted valued partner in the delivery of healthcare to patients.Position Summary:Working independently, the Medical Director is capable of fully leading designated aspects of the Medical Affairs strategic planning process and its implementation on behalf of the Global Medical Affairs Leader. The scope of the role therefore mirrors the full scope of the Global Medical Affairs Leader (GMAL) role, to whom s/he is accountable. This may include the following activities:
  • Plays an integral role in building/ optimising the Global Medical Affairs Plan (MAP) and Integrated Evidence Plan (IEP) for the relevant asset/ indication(s).
  • Works closely with the Physician Project Leader and Medicine Development Leader to optimise development plans.
  • Drives delivery of designated above-country elements of the MAP e.g. Advisory Boards; Symposia.
  • Partners with commercial colleagues to optimise brand campaigns and launches in the Franchise Local Operating Companies (LOCs).
  • Drives the development and approval of promotional and training materials.
  • Delivers the evidence needs for that asset on behalf of the GMAL in partnership with R&D:
  • Drives the efficient working of the Integrated Evidence Team; ensuring insights from Franchise LOCs are integrated appropriately to inform the IEP.
  • Reviews local GSK-sponsored and Investigator Sponsored Study (ISS) proposals from Franchise LOCs to assess their scientific merit and strategic need, liaising with R&D technical experts.
  • Accountable for the development of assigned Franchise study protocols.
  • Drives excellence in Scientific Engagement (SE) with key stakeholders (HCPs, Patients, Payors and Regulators) to gain a deep understanding of customer needs.
  • Provides medical expertise in support of compassionate use/expanded access programs
  • Deputizes regularly for the GMAL as required.
    • Key responsibilities:
  • Gathers medical insights from the Franchise Local Operating Companies (LOCs) and external stakeholders (HCP’s, Patients, Payors and Regulators) to shape the integrated evidence strategy and plan.
  • Leads Advisory Board design and discussion, as delegated by the GMAL, ensuring compliance with SE governance and documentation requirements (Approval Templates; GLASSES etc).
  • Inputs to the design and delivery of phase 3b/ 4 studies, including post-approval commitments, coordinating with relevant R&D technical experts e.g. Global Health Organization and Epidemiology as required.
  • Facilitates preparation for the aPIB review/ Brand Planning processes, ensuring compliance with timelines and mandated global templates to ensure consistency across Franchises/ Franchise LOCs.
  • Plays an integral role in the development and approval of promotional campaigns and materials, ensuring compliance with all relevant codes and system requirements (ABPI, Zinc MAPs etc).
  • Develops and reviews publications / abstracts/ posters related to the product, key competitors and relevant disease area(s). Ensures the Data Dissemination Plan (DPP) is maintained in Datavision.
  • Supports the GMAL in communicating effectively the clinical and market access data for their asset to the Franchise LOCs; ensures a robust understanding of risk: benefit.
  • Enhances local tactical plans and shares best practices to support Launch Excellence.
  • Supports the GMAL in providing medical governance oversight for the asset, including leading the management of product-related issues/ crises with potential impact on patient safety.
  • Will support the GMAL in effective management of the medical budget (MAP and IEP) for that asset.
    • Additional Responsibilities:
  • High level of responsibility for the successful delivery of critical projects and processes in the Franchise.
  • Responsible for building and driving the global Medical Affairs strategy and IEP for the asset, on behalf of the GMAL
  • Building credibility through the richness of his/her content expertise.
  • Responsible for the successful delivery of Medical Affairs plans in accordance with GSK and statutory requirements.
  • Responsible for driving excellence in external engagement - building credibility with, and insights through, a strong external network.
  • Ensures appropriate medical governance including the management of product-related issues with potential impact on patient safety.
    • Why youBasic Qualifications:
  • Medical Doctor- Board Certification (or equivalent credentials) in Oncology.Industry and/or clinical experience in the oncology therapeuti

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