Director, Oncology Clinical Pharmacology MIDD AI/ML
Tasks
- Apply drug disease modeling longitudinal exposure response analysis and model based meta analysis
- Collaborate across matrix teams to innovate methodologies design efficiencies and create value
- Conduct exposure response analysis and simulation based trial design
- Contribute to clinical program design trial protocols analysis plans study reports and regulatory submissions
- Define model based development strategies for oncology projects
- Implement best practices and lessons learned for clinical pharmacology modeling and simulation
- Perform dose selection using population PK modeling
- Present and defend model based approach outcomes to governance boards and regulatory agencies
- Publish and present model informed drug discovery and development externally
- Use quantitative systems pharmacology and AI ML informed analyses
- Write or review clinical pharmacology components of regulatory documents and responses
Perks/Benefits
- Health insurance
- Paid Holidays
- Paid caregiver leave
- Paid parental leave
- Retirement benefits
- Vacation
Skills/Tech-stack
AI machine learning | Clinical Trial Simulation | Clinical trial | Disease Modeling | Dose selection | Drug Disease Modeling | Drug development | Exposure-response | Exposure-response modeling | Longitudinal Modeling | Machine Learning | Mechanistic modeling | Meta-Analysis | Model-based meta-analysis | Model-informed drug development | Nonmem | Pharmacodynamics | Pharmacokinetics | Population PK | Quantitative systems | Quantitative systems pharmacology | R | Regulatory documentation | Response Modeling | Systems pharmacology | Trial simulation
Education
Doctor of Pharmacy (PharmD) | Master of Engineering | Master of Science | PhD
Regions
Countries
States
Cities
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