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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, USA - Pennsylvania - Philadelphia

Posted Date:
Apr


Are you interested in a highly visible Medical Affairs role that allows you to be ambitious for patients and contribute to the advancement of novel vaccines with the potential for substantive public health impact? If so, this role could be an ideal opportunity to explore We are looking to recruit a Senior Medical Manager, Global Medical Affairs - Pneumococcal MAPS Vaccine Franchise.


About the position


Global Medical Affairs (GMA) facilitates the understanding of the value of our vaccines, the science behind them and the public health impact they can offer by developing and executing global scientific and access strategies, based on evidence gaps identified and insights gathered from scientific and patient communities.


The GMA team is a dynamic, inclusive and diverse group of dedicated medical affairs professionals who are passionate and proud about what they do and the impact their work makes to patients, HCPs, public health and colleagues around the world.


As a Senior Manager, Global Medical Affairs, you will be responsible to support the development and implementation of the global medical scientific strategic plan 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.

Provide Medical Affairs expertise, scientific evidence, access focus and insights from external stakeholders to cross-functional teams within the organization. Ensure optimal evidence generation strategies are in to enable successful development, registration, access, and overall launch readiness.

What will be some of your responsibilities?

  • Contribute 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.
  • Develop and implement 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
  • Support the development, review, approval, and dissemination of medical material in collaboration with global, regional, and countrybased medical colleagues
  • Drive excellence in scientific engagement with key stakeholders (External Experts, HCPs, Patients, Payers and Regulators) and maintains excellent professional relationships
  • Provide expert knowledge of data and literature related to the asset(s)/project(s); identify important publications for communication to medical network and project team, prepare position papers, rebuttals, feedback on literature selection
  • Under the supervision of the GMPL, contribute to the medical communication strategy for the assigned areas of work, including strategic publication planning; codevelop and implement integrated scientific medical communication plan
  • Develop new medical affairs communication and training materials under the appropriate approval framework, in compliance with Scientific Engagement principles, GSK's Code of Practice and GSK values
  • Work in collaboration with medical operations team and manages agency partners as required depending on services and activities being provided required depending on services and activities being provided
  • You ensure that all communications are scientifically accurate, balanced, remain aligned with product strategy, and compliant to applicable laws and regulations

_ 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, compliance and legal framework which underpins all of GSK's interactions with the external