Director, Quantitative Pharmacology and Pharmacometrics – Oncology
USA - Pennsylvania - North Wales (Upper Gwynedd), United States
R
USD 190K-300K Executive-level Full Time
Tasks
- Author regulatory documents including IND and CSR
- Build exposure response models
- Create quantitative systems pharmacology modeling
- Design clinical trial simulation
- Develop and execute model based analyses including translational PK PD
- Develop comparator modeling
- Develop disease progression models
- Develop population pharmacokinetic models
- Frame critical questions and strategy for model based analyses
- Maintain knowledge of global regulatory expectations
- Mentor and supervise junior staff
- Model tumor size and survival
- Represent QP2 IO at regulatory meetings
- Serve as expert representative for QP2 IO on oncology development teams
Perks/Benefits
- 401k matching
- Annual bonus
- Dental insurance
- Long-term incentive
- Medical insurance
- Paid Holidays
- Paid sick days
- Vacation
- Vision insurance
Skills/Tech-stack
Biostatistics | Clinical Pharmacology | Clinical Trial Design | Clinical Trial Simulation | Clinical trial | Comparator Modeling | Data Modeling | Data Visualization | Disease progression | Disease progression modeling | Exposure-response | Exposure-response modeling | Growth modeling | IND | MATLAB | Monolix | NDA | Nonmem | Pharmacodynamic modeling | Pharmacokinetic Pharmacodynamic | Pharmacokinetic modeling | Pharmacokinetic pharmacodynamic modeling | Population Pharmacokinetic Modeling | Quantitative systems | Quantitative systems pharmacology | R | Regulatory writing | Response Modeling | Stakeholder management | Statistics | Survival Modeling | Systems pharmacology | Trial design | Trial simulation | Tumor growth modeling
Education
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