Director, Quantitative Pharmacology and Pharmacometrics – Oncology
USA - New Jersey - Rahway, United States
USD 190K-300K Executive-level Full Time
Tasks
- Author regulatory documents for IND and NDA submissions
- Build and apply population pharmacokinetic models
- Design and simulate clinical trials
- Develop and execute model based analyses
- Develop disease progression models
- Develop exposure response models
- Develop quantitative systems pharmacology models
- Frame critical questions and strategy for optimizing model based analyses
- Mentor and supervise junior staff
- Model tumor size and survival
- Perform comparator modeling
- Perform translational PKPD analyses
- Represent QP2 IO at regulatory meetings
- Serve as expert representative for oncology development teams
Perks/Benefits
- N/A
Skills/Tech-stack
Biostatistics | CTD | Clinical Trial Design | Clinical study | Clinical study reports | Clinical trial | Clinical trial design simulation | Data Modeling | Data Visualization | Design simulation | Disease progression | Disease progression modeling | Drug development | Experimental Design | Exposure-response | Exposure-response modeling | Growth modeling | IND | MATLAB | Model-Based Drug Development | Monolix | NDA | Nonmem | Pharmacodynamics | Pharmacokinetics | Pharmacometrics | Population pharmacokinetics | Quantitative systems | Quantitative systems pharmacology | R | Regulatory documentation | Response Modeling | Statistical Analysis | Survival Modeling | Systems pharmacology | Translational medicine | Tumor growth modeling
Education
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