Early Medical Lead, Specialty Medicine

Job Purpose

The EML role provides medical leadership to support the progression of assets (Medicines or vaccines) to the Commit to Phase 2 decision gate, or beyond, with indication sequencing, population segmentation and evidence generation plans informed by appropriately prioritised Medical Affairs insights.

This is a unique opportunity for an experienced, innovative and motivated Medical Affairs leader to provide strategic medical leadership for the portfolio of assets. This is a critical role expected to enable better informed decision making for portfolio progression, earlier incorporation of prioritised medical insights into evidence planning, differentiation and launch readiness, and more rapid progress through early and late clinical development.

• To bring critical Medical Affairs leadership to our assets in the early Specialty Care pipeline supporting programs from the Candidate Selection milestone through to Commit to Phase 2 or the appointment of an asset-specific Global Medical Strategy Lead.
• Working closely with the Medicines Development Lead, Medicines Commercialisation Lead, (or EDL and PPSG director as appropriate) and others to plan a reimbursable file, and optimise launch and life cycle strategy, including key input to and, once a launch commitment is secured, leadership of the Integrated Evidence Team.
• Provide targeted, focused medical leadership to a potentially diverse portfolio of innovative assets focused within aligned disease areas: provide strategic medical insights into R&D and commercialization strategies; profiling patient pathways; mapping the treatment landscape and how it may evolve in the lifecycle of the asset; identifying gaps and opportunities based on emerging data, competitor activity and understanding of diverse healthcare systems;
  
  lead on strategies to shape the future practice of medicine within specified and related disease areas.
• Contributing expertise in scientific issues related to clinical development, study design, data interpretation and study conclusions.
• Deploying strong analytical thinking to quickly assess large amounts of information and distil into key messages and actions.
• Providing strategic input opinion based on broad knowledge and close study of disease and emerging external environment, with clear focus on patients and unmet medical need. Engage and collaborate with external experts to identify key medical unmet needs, physician perspectives, treatment landscape and payer priorities.
• Connect closely with LOC Medical Affairs, ensuring key market insights are captured and reflected in strategies in a timely way and are used to validate asset and recommendation assumptions during the technical and commercial review process.

Ensure strategic alignment with clinical development and central and regional partner functions, to develop and optimize the medicine profile and evidence generation plans in support of the scientific value proposition of assigned assets and aligns resource needs.

Leadership of the global scientific communication strategy for the asset, including at scientific congresses, advisory boards or other events where appropriate. Drives excellence in scientific engagement with key stakeholders (HCPs, Patients, Payers and Regulators) to gather medical insights and build a deep understanding of customer needs to inform and shape the portfolio’s development programme.

Providing Medical input to the review of Business Development opportunities where required, including but not limited to: determining clinical value through working with external expert partners; input into determining the patient population and ensuring the lead indication fits the unmet need; determining readiness of the clinical environments for the innovation and what work (incl. EG) must be carried out to shape the practice of medicine;

consider the overall IEP and ensure wider understanding of the total “cost” of an asset acquisition is considered.

Taking accountability for the asset’s medical governance and for approval of materials and activities to ensure they are compliant with GSK Code of Practice, standard operating procedures, and with…