Qui sommes-nous ?
Pierre Fabre est le 2ème laboratoire dermo-cosmétique mondial, le 2ème groupe pharmaceutique privé français et le leader des produits vendus hors prescription dans les pharmacies en France.
Son portefeuille compte plusieurs franchises médicales et marques internationales dont Pierre Fabre Oncologie, Pierre Fabre Dermatologie, Eau Thermale Avène, Klorane, Ducray, René Furterer, A-Derma, Naturactive et Pierre Fabre Oral Care.
Implanté depuis toujours en région Occitanie, fabricant plus de 95% de ses produits en France, le groupe emploie près de 10 000 collaborateurs dans le monde et distribue ses produits dans quelque 130 pays. Pierre Fabre est détenu à 86% par la Fondation Pierre Fabre, une fondation reconnue d’utilité publique, et secondairement par ses collaborateurs à travers un plan d’actionnariat salarié.
En 2021, Ecocert Environnement a évalué la démarche de responsabilité sociétale et environnementale du Groupe selon la norme ISO 26000 du développement durable et lui a attribué le niveau « Excellence ».
Pierre Fabre est reconnu comme l’un des « Meilleurs Employeurs du Monde 2021 » par Forbes. Notre groupe est classé dans le Top 6 de l’industrie cosmétique et dans le Top 7 de l’industrie pharmaceutique dans le monde. Nous sommes convaincus que notre engagement et notre passion font préserver notre indépendance et vivre notre raison d'être.
Votre mission
Founded in the early 1960s, Pierre Fabre Laboratories’ R&D activities have steadily been advancing for over 50 years, encompassing a broad array of therapeutic solutions. Pierre Fabre’s holistic approach to health and well-being is deeply rooted in our philosophy, signified by therapies ranging from oncology to dermatology, other chronic illnesses and dermo-cosmetics.
Our group has had solid experience in oncology since 1978. We have targeted therapies for the following diseases melanoma, breast cancer, colorectal cancer, lung cancer and T-cell immunotherapy for hematological malignancies.
Research is done both in our own research center, the Oncopole, in Toulouse, and through intensive cooperation with partner companies.
The key role of the Market Access department is to obtain and maintain access to and reimbursement of our innovative treatments. In this context, our Benelux Subsidiary, located in Brussels, is looking for a Market Access intern to join a dynamic team.
The internship would ideally start from March 2025 for a duration of 6 months.
The mission will be:
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Develop scientific knowledge of the therapeutic areas (oncology);
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Understand the Belgian, Netherlands and Luxembourg Healthcare system’s organizational structure and the decision-making process;
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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;
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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;
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Collaborate extensively with the medical and business teams and to support the reimbursement negotiation & processes;
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Understand, follow and implement administrative and political mechanisms as well as the pricing regulations with internal key stakeholders for the Benelux;
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Participate to various projects simultaneously across different therapeutic areas in conjunction with relevant Brand Teams .
Qui êtes-vous ?-
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.
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You have an Interest in the Belgian or NE / Lux health care sector.
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You have basic knowledge about HTA/economic evaluation in healthcare and pharmaceutical market access.
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Experience in regulatory or regulatory affairs is an asset.
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You have strong analytical and project management skills.
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You are detail-oriented.
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You demonstrate an ability in scientific value-based communication (medical writing).
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You can understand and interpret clinical trials (RCT’s) in terms of research design, methodology and results.
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You are enthusiastic about working towards providing patient access to innovative treatments and carry out an attitude as such.
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You are able to work independently, manage multiple projects, set priorities and meet deadlines.
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You master the Microsoft Office package (Excel ...).
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You speak Dutch and English/or French.
Nous sommes convaincus que la diversité est une source d’épanouissement, d’équilibre social et de complémentarité pour nos collaborateurs, nos offres sont donc ouvertes à toutes et tous sans restriction.