Director, Quantitative Pharmacology and Pharmacometrics – Oncology
USA - New Jersey - Rahway, United States
USD 190K-300K Executive-level Full Time
Tasks
- Author regulatory documents for oncology small molecules and biologics
- Build exposure response models
- Build population pharmacokinetic models
- Develop and execute model based analyses
- Develop disease progression models
- Develop quantitative systems pharmacology models
- Frame critical questions and strategy for model based analyses
- Mentor and supervise junior staff
- Model tumor size and survival
- Perform translational PK PD analyses
- Represent QP2 IO at regulatory meetings
- Run comparator modeling
- Serve as expert representative for oncology development teams
- Simulate clinical trial designs
Perks/Benefits
- N/A
Skills/Tech-stack
Biostatistics | Clinical Pharmacology | Clinical Trial Simulation | Clinical trial | Comparator Modeling | Data Analysis | Data Modeling | Data Visualization | Disease progression | Disease progression modeling | Drug development | Experimental Design | Exposure-response | Exposure-response modeling | MATLAB | Monolix | Nonmem | PK/PD | Pharmacodynamics | Pharmacokinetics | Pharmacometrics | Population pharmacokinetics | Program Leadership | Quantitative systems | Quantitative systems pharmacology | R | Response Modeling | Stakeholder management | Systems pharmacology | Translational PK PD | Trial simulation
Education
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