Senior Manager, Global Medical Affairs
il y a 1 semaine
Site Name:
Belgium-Wavre
Posted Date:
Feb
Healthcare professionals, payers, and patients need to be heard and understood, with access to high quality, relevant, timely and fair-balanced medical and health economic information to ensure that informed decisions are made to drive the best possible patient care.
Medical Affairs ensures that the medical needs of our customers are considered in all that we do, consistent with GSK Values.
We are responsible for deeply understanding the customer and the environment from a medical perspective so that they can ensure the clinical and economic data being developed will provide the greatest opportunity for the appropriate patients and to provide commercial with a deeper understanding of the medical relevance of the data generated.
If you are interested in role that is committed to for Phase 3b and 4 evidence generation, external and scientific engagement and internal medical advice on our medicines and the marketplace from a medical perspective_, _this Global Medical Affairs role could be an ideal opportunity to explore.
Global Medical Affairs 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, medical and patient communities.
As a Senior Global Medical Affairs Manager, you will join 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.
This role will provide YOU the opportunity to lead key activities to progress YOUR career.These responsibilities include some of the following_:
_
- Responsible to input into Medical Affairs and access strategy for the assigned product (SHINGRIX)
- Executing of the Medical Operational Plans
- Participating in or driving R&D Streams and representing the medical voice; this includes ensuring insights from regions and LOCs and key external stakeholders (vaccine recipients, physicians, payers, regulators)
- Assisting in identifying, generating medical, epidemiological, clinical (including investigator sponsored studies) and health economic outcomes and research data to create value and ensure proactive engagement with key internal and external stakeholders in line with customer needs
- Contributing to developing a clinical development strategy for phase 3b and 4 studies, including postapproval commitments, and investigator sponsored studies that supports the evidence needs of delivering or expanding the value proposition in line with customer needs
- Working in partnership with clinical development and central and regional partner functions, to optimize the clinical development plans in support of a robust file and life cycle strategy
- Responsible for ensuring that plans and activities of the assigned vaccine are implemented in a manner that is compliant with GSK's Code of Practice and GSK values
- Representing the medical voice into the vaccine development and commercial streams in alignment with the GMAL
- Ensuring 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:
- Master's degree in Science
- 5 or more years of experience in a pharmaceutical setting
- 3 or more years of project management or operational experience
- Experience in Code of Promotion and Scientific Engagement
Preferred Qualifications:
If you have the following characteristics, it would be a plus:
- At least 5 years in pharmaceutical industry, acquired through global or Regional/Local Medical Affairs or non-Medical Affairs relevant functional areas: Regulatory affairs, Clinical, epidemiology, market access, discovery
- Experience in Launch, life cycle management or early development
- Ability to input in the medical affairs and market access strategy and constructively interact crossfunctionally to build brand & project strategy
- Engaging, building and sustaining a broad and strong external (expert) network
- Experience in organizing activities involving EE's, such as symposia, CME, advisory boards
- Business acumen acquired through nonMedical Affairs relevant functional areas (Commercial, Governmental Affairs, Market Access) is an asset
- Excellent communication skills
- Experienced speaker on scientific/medical topics in fora of different audiences, including Advisory boards, public panel discussion
- Advocacy experience and interaction with governmental officials is an asset
- Strong analytical skills to be able to assess and interpret scientific data
- Ability to independently develop and review new materials based on strategy
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