Rsv Senior Medical Manager

il y a 3 semaines

Wavre, Belgique GSK Temps plein

**Site Name**: Belgium-Wavre, GSK House, USA - Massachusetts - Boston, USA - Massachusetts - Boston Central, USA - Massachusetts - Boston North, USA - Massachusetts - Boston South

**Posted Date**: Feb 16 2023

Are you looking for an exciting opportunity to drive a paradigm shift in RSV prevention through vaccination, and help shape and deliver RSV vaccine medical plan? If so, this is the opportunity for you.

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 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:

- Under the supervision of the Global of the Global Medical Affairs Portfolio Lead (GMPL), you are responsible to help develop and execute the Global Medical Affairs plan related to the older adult RSV vaccine
- 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 country-based 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); identifies important publications for communication to medical network and project team, prepares position papers, rebuttals, feed-back on literature selection
- 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
- 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 non-Medical Affairs relevant functional areas: e.g. regulatory affairs, clinical, epidemiology, market access, discovery, etc.
- 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 develop, design and implement Phase 2 & 3b /4 studies
- Experience in product launch, or life cycle management
- Interaction experience with external experts (EE’s), governmental officials or advocacy groups
- Highly developed leadership, networking, communication and influencing skills to work effectively in a complex matrix and cross-functional environment
- Proficient in managing multiple projects, budgets, and matrix interactions (internal / external consistent with each research project)
- Ability to take a solid fact-based position
- Ability to develop and review independently new materials based on strategy, core evidence documents and communication strategy

**Preferred Qualifications**:
If you have the following characteristics, it would be a plus:

- Ability to absorb, analyze and impactfully distil new clinical, epidemiological, HO, basic science information in a format adapted to the target audience
- Relevant experience vaccinology, epidemiology, and market access/NITAG interaction is a strong asset
- Experience in organizing activities involving EE’s, such as advisory boards and symposia, or advocacy groups
- Excellent communication skills
- Experience with review & approval processes in a highly regulated setting
- Experience in interaction and management of external vendors
- Proficiency in common office programs Word, PPT, Excel
- Fluent in English

**_ Why GSK?_**:
**Uniting science, technology and talent to get ahead of disease together**:
GSK is a global bioph

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