The role is part of a France / Benelux Medical Affairs structure. The Benelux organization is being built progressively, and the first MSLs will have a strategic impact on how the medical presence is shaped locally. The initial therapeutic focus is chronic insomnia, with a strong emphasis on non-promotional scientific exchange, KOL engagement and sleep center mapping.
Your future role:
As Medical Science Liaison for North Belgium / Flanders, you will become the scientific field expert for your territory. Your role will be to engage in high-quality, balanced, non-promotional scientific discussions with healthcare professionals and key opinion leaders. You will help build the medical network in your region and provide valuable insights to the internal Medical Affairs team.
You will be involved before the broader commercial structure is launched, which means your work will be foundational. You will identify relevant sleep centers, map stakeholders, understand local treatment pathways, listen to the needs and challenges of healthcare professionals and develop trusted scientific relationships.
A structured onboarding and scientific training period of approximately two months is planned. Previous experience in sleep medicine or CNS is therefore not mandatory. What matters most is your ability to learn quickly, understand scientific data, synthesize complex information and communicate it in a clear and engaging way.
Your responsibilities will include:
- Building and developing strong scientific relationships with healthcare professionals, KOLs, researchers and sleep centers in North Belgium / Flanders.
- Providing credible, fair, balanced and non-promotional scientific information.
- Mapping relevant centers, stakeholders and scientific opportunities within the territory.
- Understanding the perspectives, challenges and needs of healthcare professionals in patient care.
- Developing and executing a dynamic territory action plan in line with the broader Medical Affairs strategy.
- Acting as a scientific expert through regular literature review, scientific monitoring and congress participation.
- Collecting and sharing field insights, including KOL and site profiling.
- Participating in regional, national and international scientific events when relevant.
- Supporting internal scientific training and cross-functional collaboration with medical, marketing or field teams where appropriate.
- Supporting the identification of potential investigators, research opportunities or clinical sites.
- Using internal tools such as Veeva CRM to document and share relevant information.
- Working in full compliance with internal procedures, pharmacovigilance requirements, medical information standards and Belgian ethical rules.
