Pfizer Vaccines Sr Medical Advisor Belgium in Brussels, La Plaine, Belgium


  • Through interaction with internal and external stakeholders drive value growth of Pfizer Vaccines in Belgium, using a scientific approach and taking all medical as well as compliance and regulatory aspects into account to establish the role for assigned product/products in the health care system. This includes not only the data on the products but also the medical environment in which the products are or could be used.


  • Be responsible for assigned Pfizer product/products in Belgium and, in collaboration with other internal colleagues, identify possibilities and relevant activities to drive business. This includes, but is not limited to:

  • Health care professionals and other relevant external stakeholders, disseminating information of medical relevance concerning the products of her/his responsibility and the medical implications for current practices through advisory boards, symposia and other meetings and ways of communication.

  • Interactions with relevant health care professionals to stimulate research efforts to establish a wider knowledge about the products and their optimal use. Actively work for initiation of Investigator Initiated Research, Non-interventional Studies, and site selection of global company sponsored studies within the local market.

  • Timely provide accurate and medically sound responses to enquiries by the medical societies and other stakeholders concerning products within her/his responsibility.

  • Ensure that marketing material is medically relevant as well as compliant with the regulatory requirements.

  • In collaboration with regulatory department ensure correct wording in SPC and other documents.

  • Provide medical/scientific expertise for formulary applications, HTA assessments and tender processes.

  • Make the 2019 medical plan based on identified needs, and in line with country and International Developed Markets (IDM) strategies, taking into account product life cycle and providing budgeting of scientific projects.

  • Develop and maintain a strong network of Key Opinion Leaders (KOL) within the assigned therapeutic area.

  • Actively participate in the Medical Affairs team and relevant meetings and projects at the IDM-level in order to be updated on the current development of the therapeutic area and influence and contribute to future development.

  • Build strategic partnerships with internal collaborators, specifically Patient&Health Impact/Market Access/Health Outcomes, Brand Managers, and the IDM and Global Vaccines teams.

  • Provide highly innovative solutions, and routinely exercises independent judgment in developing methods, techniques and criteria for achieving objectives.

  • Develop strategy and set functional policy and direction.


  • Technical

  • General business insight and high level of industry understanding.

  • Additional specialized knowledge within relevant therapeutic area.

  • Managerial

  • Independence and ability to work in an international setting in a matrix organization.

  • Performance driven with professional demeanor and strong team-work ability.

  • Excellent social skills.

  • Ability to travel.

  • Certifications

  • 4-6 years of related clinical or scientific experience.

  • Education

  • Medical Doctor or other relevant Academic degree with good scientific and/or clinical skills.

  • Fluent in French, Flemish and English.

  • Experience

  • Several years as medical advisor with expert knowledge.

  • Clinical trial or research experience.


A temporary contract for 1 year is offered.

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.