Population PK/Pharmacometrics Modeler- CDI- H/F

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

We are seeking a Population PK/Pharmacometrics Modeler to join the Pharmacokinetics and Toxicology team within the Pierre Fabre R&D Pharma in Toulouse to support oncology programs (Langlade site, Oncopole).

Who You are

You are a proactive pharmacometrician who translates clinical trial data into strategic insights that shape dosing strategies, trial designs, and regulatory submissions. You combine deep technical expertise in population modeling with the ability to distill complex exposure-response relationships into clear recommendations for clinical teams, regulators, and senior leadership. You thrive in collaborative environments where your quantitative analyses directly influence decisions from Phase 1 dose escalation schemes to pivotal trial endpoints. You understand that the value of a model lies not in its mathematical elegance but in its ability to reduce uncertainty and accelerate patient access to effective therapies.

Your role within a pioneering company in full expansion:

• Lead population PK/PD modeling strategies and translate findings into clear recommendations to drive critical decisions across clinical development programs
• Develop and qualify pharmacometrics analyses with emphasis on population PK/PD modeling and exposure-response analysis in oncology
• Drive and coordinate the integration of pharmacometrics analyses in the drug development process to mitigate risks early and support data-driven decision-making
• Identify opportunities where pharmacometrics analyses can contribute to a better understanding of pharmacokinetics, pharmacodynamics, safety, and efficacy
• Serve as lead author and key contributor for pharmacometrics sections of clinical and regulatory documents (e.g., briefing books, summaries of clinical pharmacology/efficacy/safety, and responses to Health Authority questions)
• Represent the team at global regulatory hearings/advisory committee meetings and other global regulatory interactions
• Mentor and guide colleagues on pharmacometrics methodology
• Contribute to scientific publication

This position is compatible with teleworking up to 2 days a week according to company rules.

We offer an attractive remuneration/benefits package: Incentives, profit-sharing, Pierre Fabre shareholding with matching contribution, health and provident insurance, 16 days of holidays (RTT) in addition to 25 days of personal holidays, public transport participation...

Qui êtes-vous ?

Your skills at the service of innovative projects:

Required Qualifications:

• PhD in Pharmaceutical Sciences, Pharmacometrics, Biostatistics, Applied Mathematics, or a related quantitative field
• Minimum 5+ years of hands-on population PK modeling experience in the pharmaceutical industry
• Expert-level proficiency in NONMEM; familiarity with other mixed-effects modeling tools, such as Monolix, is a plus
• Extensive experience with advanced population PK/PD methodology
• Strong programming skills in R or Python for data manipulation, exploratory analysis, diagnostics, and visualization
• Experience in supporting regulatory submissions (IND, NDA/BLA) including preparation of modeling sections and responding to health authorities
• Excellent interpersonal skills and the ability to work in cross-functional teams
• Excellent written and verbal skills in English

Preferred Qualifications:

• Proven track record of delivering pharmacometrics analyses that influenced clinical development or regulatory decisions
• Experience with model-based meta-analysis, Bayesian trial design, or novel exposure-response methods
• Understanding of oncology drug development is highly desirable
• Experience in modeling multiple therapeutic modalities beyond small molecules (biologics, targeted therapies, ADCs) is a plus

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.