Senior Director, MIDD & Clinical Pharmacology (CV/Metabolic)

GlaxoSmithKline; Durham (NC); Sur place; USD 223 000 - 371 000; Plein temps

Avantages offerts par ce poste

Annual bonus

Long-term incentive program

Health insurance

Retirement benefits

Paid holidays

Vacation

Résumé du poste

GlaxoSmithKline seeks a Senior Director of Cardiovascular and Metabolic Diseases, Clinical Pharmacology Modeling and Simulation to lead Model Informed Drug Development across RIIRU, guiding strategy from first-in-human studies to lifecycle management. The role reports to RIIRU and sits within CPQM to advance quantitative pharmacology and AI integration.

You will design robust MIDD evidence strategies, coordinate CPMS activities across assets, and ensure regulatory-ready pharmacology content

Qualifications

• PhD, MD or PharmD required.
• 8+ years in clinical pharmacology, modelling/simulation and drug development.
• Experience in pharmacometrics applied to clinical questions.
• Experience working with senior stakeholders in cross-functional settings.
• Experience in Cardiovascular and Metabolic Diseases therapy areas.

Responsabilités

• Design and implement Model Informed and Clinical Pharmacology strategies across RIIRU programs.
• Coordinate CPMS activities and align CPMS/CPQM priorities globally.
• Approve study designs, analyses, and regulatory documents; ensure regulatory readiness.
• Build cross-functional partnerships with CPQM functions and other departments.
• Lead external engagement to raise GSK's profile in MIDD and clinical pharmacology.

Connaissances

Pharmacology

Clinical pharmacology

Pharmacometrics

MIDD

Leadership

Cross-functional collaboration

Formation

PhD/MD/PharmD

Description du poste

GlaxoSmithKline seeks a Senior Director of Cardiovascular and Metabolic Diseases, Clinical Pharmacology Modeling and Simulation to lead Model Informed Drug Development across RIIRU, guiding strategy from first-in-human studies to lifecycle management. The role reports to RIIRU and sits within CPQM to advance quantitative pharmacology and AI integration.

You will design robust MIDD evidence strategies, coordinate CPMS activities across assets, and ensure regulatory-ready pharmacology content