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Senior Medical Manager, Global Medical Affairs

Il y a 3 mois

Wavre, Wallonie, Belgique GSK Temps plein

Site Name:
Belgium-Wavre

Posted Date:
Mar 9 2023


As a Senior Manager, Global Medical Affairs, you will be responsible to support the development and implementation of the global medical scientific strategic plan for assigned assets by integrating insights from HCPs, patients and the health care landscape into the asset profiles in alignment with the global medical accountabilities as per the GSK integrated asset operating model.

This role will provide you the opportunity to lead key activities to progress your career.

These responsibilities include some of the following:

  • Provide Medical Affairs expertise, scientific evidence, access focus and insights from external stakeholders to crossfunctional teams within the organisation. Ensure optimal evidence generation strategies are in place for assigned assets to enable successful development, registration, access, and overall launch readiness.
  • Under the supervision of the Global Medical Affairs Portfolio Lead (GMPL), executes the Global Medical Affairs Plan (MAP) for the relevant asset(s)/ indication(s). Drives delivery of designated elements of the MAP.
  • Contributes to the medical affairs section of the integrated asset plan (IAP) and Integrated Evidence Plan (IEP) in alignment with global medical accountabilities e.g. disease landscape, external engagement plans etc.
  • Develops and implements agreed elements of External Expert Engagement Plans in alignment with Scientific Engagement principles and relevant GSK policies; external activities could include Advisory boards, External Medical round tables, HCP scientific meetings.
  • Provides medical/ scientific insights and leadership to crossfunctional teams working on assigned assets, to validate assumptions and recommendations during the technical and commercial review process. Brings expertise to strategic discussions regarding the evidence requirements by leveraging an understanding of anticipated changes in disease landscape, treatment paradigm and evolution of Policy/Payor scenarios in key LOCs to optimise data generation and lifecycle management plans globally.
  • Assists in identifying and generating medical, epidemiological, clinical and health economic outcomes and research data to create value and ensure proactive engagement with key internal and external stakeholders to ensure integration and alignment of data/ activities in line with customer and patient needs. Contributes to the interpretation of the data to provide medical input to asset development, scientific communication and commercial strategy and materials
  • Provides expert knowledge of data and literature related to the asset(s)/project(s); identifies important publications for communication to medical network and project team, prepares position papers, rebuttals, feedback on literature selection
  • Critically appraises, reviews and recommends changes to publications, commercial and clinical documents for alignment to strategy, clarity of messages and scientific accuracy.
  • Ensures that plans and activities are implemented in a manner that is compliant with Scientific Engagement principles, GSK's Code of Practice and GSK values and that all communications (internal and external) are scientifically accurate, balanced, aligned with asset strategy, and compliant to applicable laws and regulations.
  • Under the supervision of the GMPL, contributes to the medical communication strategy for the assigned areas of work, including long term communication / publication planning. Codevelops and implements integrated scientific medical communication plan,
  • Works in collaboration with medical operations team and manages agency partners as required depending on services and activities being provided.

_ Why you?_:

Basic Qualifications:

We are looking for professionals with these required skills to achieve our goals:

  • Medical Doctor, PharmD, PhD in life sciences. Specialization in vaccinology, immunology, infectious diseases, microbiology, virology, life sciences, public health, health economic policy is preferred.
  • At least 5 years industry and/or clinical experience in the relevant field, acquired through global or regional/Local Medical Affairs or nonMedical Affairs relevant functional areas: e.g. regulatory affairs, clinical, epidemiology, market access, discovery etc.
  • Business acumen acquired through work with nonMedical Affairs relevant functional areas (Commercial, Governmental Affairs, Market Access)
  • Knowledge and understanding of the drug/ vaccine development process from asset inception through lifecycle management. Strong analytical skills to be able to assess and interpret scientific data and ability to support the development, design and implementation of Phase 2 & 3b /4 studies.
  • Experience in product launch, life cycle management or early development
  • Demonstrated ability in engaging, building and sustaining a broad and strong external (expert) network.
  • Clear understanding of the ethical, regulatory,