Pierre Fabre is the 2nd largest dermo-cosmetics laboratory in the world, the 2nd largest private French pharmaceutical group and the market leader in France for products sold over the counter in pharmacies.

Its portfolio includes several medical franchises and international brands including Pierre Fabre Oncologie, Pierre Fabre Dermatologie, Eau Thermale Avène, Klorane, Ducray, René Furterer, A-Derma, Naturactive, Pierre Fabre Oral Care. 

Established in the Occitanie region since its creation, and manufacturing over 95% of its products in France, the Group employs some 10,000 people worldwide. Its products are distributed in about 130 countries. 86% of the Pierre Fabre Group is held by the Pierre Fabre Foundation, a government-recognized public-interest foundation, while a smaller share is owned by its employees via an employee stock ownership plan. 

In 2019, Ecocert Environment assessed the Group’s corporate social and environmental responsibility approach in accordance with the ISO 26000 sustainable development standard and awarded it the “Excellence” level.

Pierre Fabre is recognized as one of the "World's Best Employers 2021" by Forbes. Our group is ranked in the Top 3 in the cosmetics industry and in the Top 10 in the pharmaceutical industry worldwide. 

Your mission

• Develop scientific knowledge of the therapeutic areas (oncology)
• Understand the Belgian, Netherlands and Luxembourg Healthcare system’s organizational structure and the decision-making process
• Create a based value communication / dossier writing (e.g. clinical evidence, local epidemiology, local guidelines etc,) to develop reimbursement submissions or revisions to meet country-specific market access needs and requirements in the BeNeLux region
• Support adaptation for regional market access and pricing materials (regional and global value dossiers, economic evaluations/Health Technology Assessment  (HTA) e.g. cost-effectiveness analysis and budget impact models) for Pierre Fabre to develop reimbursement submissions and subsequent launches in the Benelux region
• Collaborate extensively with the medical and business teams and to support the reimbursement negotiation & processes
• Understand, follow and implement administrative and political mechanisms as well as the pricing regulations with internal key stakeholders for the Benelux
• Participate to various projects simultaneously across different therapeutic areas in conjunction with relevant Brand Teams

• You are pursuing or finalized a  Master of Science degree: PharmD, Epidemiology, Business engineering, Public Health, Pharmacy, Health Economics, Health Outcomes Research, Health Services Research, or other market access related program.
• You have an Interest in the Belgian or NE / Lux health care sector.
• You have basic knowledge about HTA/economic evaluation in healthcare and pharmaceutical market access.
• Experience in regulatory or regulatory affairs is an asset.
• You have strong analytical and project management skills.
• You are detail-oriented.
• You demonstrate an ability in scientific value-based communication (medical writing).
• You can understand and interpret clinical trials (RCT’s) in terms of research design, methodology and results.
• You are enthusiastic about working towards providing patient access to innovative treatments and carry out an attitude as such.
• You are able to work independently, manage multiple projects, set priorities and meet deadlines.
• You master the Microsoft Office package (Excel ...).
• You speak Dutch and English/or French.

We are convinced that diversity is a source of fulfillment, social balance and complementarity for our employees, which is why our offers are open to all, without restriction.