Senior Medical Manager- Neisseria Vaccine

il y a 1 semaine

Wavre, Wallonie, Belgique GSK Temps plein

Site Name:
USA - Maryland - Rockville, Belgium-Wavre, Home Worker - USA

Posted Date:
Feb


Are you interested in a highly visible medical affairs role that allows you to contribute to developing a clinical development strategy, partnering with cross-functional teams that educates and shapes awareness of our medicines? If so, this Medical Affairs Manager 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 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.

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 and access strategy for the assigned product.
  • Executing of the Medical Operational Plans (MoPs).
  • Participating in or driving Access Stream for the assigned asset 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 Scientific Engagement principles, 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:

  • MD or PhD in life sciences. Specialization in Immunology, infectious diseases, microbiology, virology, life sciences, public health, health economic policy is an asset.
  • Minimum 2 years experience in medical affairs.

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, core evidence documents and communication strategy, publication experience.
  • Ability to take a solid factbased position.
  • Experience with review & approval processes in a highly regulated setting.
  • Experience of managing external vendors.
  • Why GSK?_


We're combining the power of genetic and genomic insights into what causes disease, with the speed and scale of artificial intelligence and machine learning (AI/ML) to make better predictions about who a treatment might work for, and why.

We believe this powerful combination of data and technology holds the key to fundamentally transforming medical discovery for the better, improving R&D success rates and shapin

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