Director, AI/ML MIDD Oncology Clinical Pharmacology, Modeling and Simulation
Tasks
- Apply drug disease modelling
- Apply longitudinal exposure response analysis
- Author and review clinical pharmacology regulatory submissions
- Collaborate with external partners journal publish and present
- Coordinate across matrix teams to improve methodologies and design efficiencies
- Define model based development strategies
- Design simulation based clinical trials
- Develop clinical program design trial protocols and analysis plans
- Implement modelling best practices and lessons learned
- Perform AI ML informed analyses
- Perform model based meta analysis
- Perform quantitative systems pharmacology
- Plan conduct and report exposure response analysis
- Present and defend model based approaches to governance boards
- Select dose using population PK modelling
Perks/Benefits
- Health insurance
- Paid Holidays
- Paid caregiver leave
- Paid parental leave
- Retirement benefits
- Vacation
Skills/Tech-stack
AI/ML | Disease modelling | Drug development | Drug disease modelling | Exposure-response | Exposure-response analysis | Longitudinal modelling | Mechanistic PKPD | Meta-Analysis | Model-based meta-analysis | Model-informed drug development | Nonmem | Pharmacodynamics | Pharmacokinetics | Pharmacometrics | Population PK | Quantitative systems | Quantitative systems pharmacology | R | Response analysis | Simulation based trial design | Systems pharmacology | Trial design
Education
Roles
AI | AI/ML Director | Director
Regions
Countries
States
Cities
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