Director, AI/ML MIDD for Oncology CPMS

GSK

Sint-Katelijne-Waver

Hybride

EUR 139 000 - 231 000

Plein temps

14 jours+
Générateur de candidature

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Avantages offerts par ce poste

Hybrid work model

Résumé du poste

GSK invites applications for a Director, AI/ML MIDD Oncology Clinical Pharmacology, Modeling and Simulation, to lead quantitative pharmacology activities across oncology programs.

The role focuses on delivering CPMS excellence to development projects, informing dosing and trial design, and leveraging AI/ML to advance drug discovery and development. Candidates will operate across Stevenage with planned UK relocation timelines.

Qualifications

  • A PhD in Quantitative Clinical Pharmacology or Pharmacometrics (or PharmD/Master with 4+ years)
  • 5+ years using mechanistic PKPD and longitudinal disease modelling; proficiency in NONMEM or R
  • Expertise in AI/ML applications in Clinical Pharmacology and pharmacometrics

Responsabilités

  • Define and execute model-based development strategies for oncology projects.
  • Plan, conduct and report exposure–response analysis, trial design and dose selection, and population PK modelling.
  • Apply innovative methods (drug–disease modelling, longitudinal E-R analysis, PBPK, QSP, AI/ML) to improve data use and trial efficiency.
  • Present strategy and defend model-based outcomes to governance boards and regulators.
  • Contribute to clinical program design, protocols and regulatory submissions.
  • Draft or review clinical pharmacology sections of regulatory documents to enable rapid approvals.

Connaissances

PhD in Quantitative Clinical Pharmacol
Mechanistic PKPD modelling
AI/ML in Clinical Pharmacology
NONMEM
R

Formation

PhD in Quantitative Clinical Pharmacology
PharmD or Master in related field with 4+ years experience

Outils

NONMEM
R

Description du poste

GSK invites applications for a Director, AI/ML MIDD Oncology Clinical Pharmacology, Modeling and Simulation, to lead quantitative pharmacology activities across oncology programs.

The role focuses on delivering CPMS excellence to development projects, informing dosing and trial design, and leveraging AI/ML to advance drug discovery and development. Candidates will operate across Stevenage with planned UK relocation timelines.

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