CHERCHEUR D'EMPLOI
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Senior Manager, Global Medical Affairs - Early Pipeline Vaccines
- Secteur de mon entreprise
- Pharmaceutique
- Localisation de mon entreprise
- Wavre & Rixensart
- Adresse
Site de Wavre: Av. Fleming 20, 1300 Wavre
Site de Rixensart: Rue de l'Institut 89, 1330 Rixensart
Santé physique & mentale
About the role
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.
About 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 non-Medical Affairs relevant functional areas: e.g. regulatory affairs, clinical, epidemiology, market access, discovery etc.
Business acumen acquired through work with non-Medical 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 environment; knowledge of the issues that face Pharma Industry with respect to interactions with External Experts
Highly developed leadership, networking, communication and influencing skills to work effectively in a complex matrix environment
Proficient in managing multiple projects, budgets, and matrix interactions (internal / external consistent with each research project)
Strong analytical skills to be able to assess and interpret scientific data
Ability to independently develop and review new materials based on strategy, core evidence documents and communication strategy, publication experience
Experience with review & approval processes in a highly regulated setting
Experience of managing external vendors
About the responsibilities
Under the supervision of the Global Medical Affairs Portfolio Lead (GMPL), you will provide global medical affairs leadership for an assigned portfolio of assets in early development and research, which may include viral, bacterial, or targeted immunotherapies assets providing strategic medical insights into R&D and commercialization strategies
In collaboration with the medical director(s), you are responsible to help develop and execute the Global Medical Affairs plan related to the assigned assets
You will 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, digital platforms, External Medical round tables, HCP scientific meetings
You will support the development, review, approval, and dissemination of medical material in collaboration with global, regional, and country-based medical colleagues
You will rive excellence in scientific engagement with key stakeholders (External Experts, HCPs, Patients, Payers and Regulators) and maintains excellent professional relationships
You will sound medical voice of GSK, and will be able to represent the medical affairs team externally according to the level of experience and subject matter expertise. You will gather medical insights and builds a deep understanding of external stakeholders’ needs to inform and shape the asset’s development program
You will 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, feed-back on literature selection.
Under the supervision of the GMPL, and in collaboration with the medical director(s), you will contribute to the medical communication strategy for the assigned assets, including strategic publication planning; co-develop and implement integrated scientific medical communication plan
You will 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
You will 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 will ensure that all communications are scientifically accurate, balanced, remain aligned with product strategy, and compliant to applicable laws and regulations