Senior Quantitative Clinical Pharmacology Lead – Oncology

Pierre Fabre Laboratories

Toulouse

Hybride

EUR 140 000 - 190 000

Plein temps

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Avantages offerts par ce poste

Profit-sharing
Company shareholding with matching
Health insurance
Telework up to 2 days/week

Résumé du poste

Pierre Fabre Laboratories in Toulouse is seeking a Senior Quantitative Clinical Pharmacology Lead to drive translational PK/PD programs from pre-IND to regulatory submissions. This role combines strategic matrix leadership with advanced Model-Informed Drug Development (MIDD) to optimize oncology programs, rare diseases and dermatology opportunities.

You will design first-in-human studies, interact with global health authorities, and oversee internal modellers and CROs to deliver high-quality

Qualifications

  • Proven ability to lead clinical pharmacology strategy across asset teams.
  • Strong modeling expertise (PopPK, PK/PD, exposure-response, PBPK, MBMA).
  • Experience in oncology-focused translational pharmacology and regulatory interactions.

Responsabilités

  • Lead PK/PD development plans from pre-IND through approval and lifecycle management.
  • Provide scientific oversight for protocols and clinical study reports.
  • Collaborate with cross-functional teams (Toxicology, Biostatistics, Regulatory) to steer programs.
  • Interact with health authorities in global regulatory interactions.

Connaissances

Strategic leadership
MIDD literacy
Oncology pharmacology
Trial design & execution
Regulatory interaction
Quantitative decision making

Formation

Ph.D./Pharm.D./M.D. in Clinical Pharmacology or related field

Description du poste

Pierre Fabre Laboratories in Toulouse is seeking a Senior Quantitative Clinical Pharmacology Lead to drive translational PK/PD programs from pre-IND to regulatory submissions. This role combines strategic matrix leadership with advanced Model-Informed Drug Development (MIDD) to optimize oncology programs, rare diseases and dermatology opportunities.

You will design first-in-human studies, interact with global health authorities, and oversee internal modellers and CROs to deliver high-quality

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