Director, Cardiovascular & Metabolic MIDD Strategy

Women In Bio; Waltham (MA); On-site; USD 188,000 - 314,000; Full time

Benefits offered by this job

Annual bonus

Health care and other insurance

Retirement benefits

Paid holidays

Paid caregiver/parental leave

Job summary

GSK is seeking a Director of Cardiovascular and Metabolic diseases in Clinical Pharmacology Modeling and Simulation. The role focuses on leading model-informed drug development across the lifecycle and partnering with CPQM, translational imaging and AI/ML teams.

The position requires a PhD/MD/PharmD with 5+ years in clinical pharmacology, modelling, and drug development. It includes working with senior stakeholders and contributing to regulatory discussions.

Qualifications

• PhD, MD or PharmD with industry clinical pharmacology experience.
• 5+ years in clinical pharmacology, modelling/simulation and drug development.
• Experience applying pharmacometrics to clinical problems.

Responsibilities

• Design and execute Model Informed and Clinical Pharmacology strategies.
• Draft and review regulatory content to support approvals and labeling.
• Collaborate across CPQM, biology, data science, clinical operations and RWE teams.
• Lead external engagement in MIDD, clinical pharmacology and AI/ML integration.

Skills

Drug Design

Drug Development

Drug Discovery Process

Drug Discovery Research

Medication Safety

Molecular Modeling

Pharmaceutical Regulatory Compliance

Pharmaceutical Sciences

Pharmacodynamics

Pharmacokinetics

Pharmacology

Pharmacometrics

Pharmacovigilance

Study Design

Target Validation

Education

PhD, MD, or PharmD

Job description

GSK is seeking a Director of Cardiovascular and Metabolic diseases in Clinical Pharmacology Modeling and Simulation. The role focuses on leading model-informed drug development across the lifecycle and partnering with CPQM, translational imaging and AI/ML teams.

The position requires a PhD/MD/PharmD with 5+ years in clinical pharmacology, modelling, and drug development. It includes working with senior stakeholders and contributing to regulatory discussions.