Pierre Fabre is the 2nd largest dermocosmetics 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 Avne Klorane Ducray Ren Furterer ADerma 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 10000 people worldwide. Its products are distributed in about 130 countries.86 of the Pierre Fabre Group is held by the Pierre Fabre Foundation a governmentrecognized publicinterest foundation while a smaller share is owned by its employees via an employee stock ownership plan.

In 2019 Ecocert Environment assessed the Groups 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 Worlds 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

GENERAL RESPONSIBILITIES

• To support the Medical Director/Medical Lead in the development of the medical strategy for disease area(s)/product(s) for which he/she is responsible (existing indications and new indications) and in its implementation.

• To be responsible for setting up and coordinating the activities of the medical plan in coordination with the various departments of the DMPC for the pathology(ies)/product(s) for which he/she is responsible.

• To set up and ensure the relevance and visibility of the brands scientific omnichannel communication.

• To develop the scientific content of medical communication materials.

• To help identify and interact with key external international contacts (HCP experts academic groups

• To write review and validate the therapeutic indications and the clinical efficacy section of the regulatory dossiers for Product Life Cycle Management (Specific: Pharma Care & DTO

KEY COLLABORATIONS

• Medical & Patient Direction

• DMPC teams (eg Clinical Platform Pharmacovigilance Medical Writing Medical insights)

• Corporate Franchise regulatory affairs Research & Development

• Country medical teams

• MSL Coordination

• International Medical Direction

KEY COMPETENCIES

• Medical Doctor pharmacist PhD scientific background master level

• At least 5 years in a medical department with medical affairs activities

• Field experience if possible

• Experience in the planned therapeutic area

• Englishfluent

Technical and transversal skills:

• Indepth medical knowledge

• Knowing how to develop a network federate it and maintain it (Health Authorities Health Professionals Learned Societies Patient Associations)

• Present scientific data results internally and externally

• Knowledge of relevant regulations and guidelines (FDA and EU) as well as experience of interactions with health authorities and market access are essential

• Excellent knowledge of the competitive environment for medicines in the market and in research and development pipelines

• Analytical and strategic thinking

• High level of ethics and integrity

Leadership Model skills:

Work transversally

Ability to work with international stakeholders

Master communication techniques

Planning of ambitious & realistic objectives and delivering accordingly

Mdecin ou Pharmacien

Ou de formation scientifique Master

Exprience dau moins 5 ans en affaires mdicales.

Exprience rglementaire requise pour le support de dossiers rglementaires de son portefeuille

Aisance en recherche bibliographique

Exprience prfrable dans le domaine des produits matures

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.