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Senior Manager, Global Medical Affairs - Early Pipeline Vaccines
看过: 140
更新日: 03-12-2025
位置: Wavre Walloon Brabant
工作类型: Full-time
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工作内容
Site Name: Belgium-WavrePosted Date: Jul 18 2023
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 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
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
GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. Getting ahead means preventing disease as well as treating it, and we aim to positively impact the health of 2.5 billion people by the end of 2030.
Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a workplace where everyone can feel a sense of belonging and thrive as set out in our Equal and Inclusive Treatment of Employees policy. We’re committed to being more proactive at all levels so that our workforce reflects the communities we work and hire in, and our GSK leadership reflects our GSK workforce.
Important notice to Employment businesses/ Agencies
GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK’s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.
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最后期限: 17-01-2026
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