Senior Director, Quantitative Pharmacology and Pharmacometrics – Immuno-Oncology
USA - New Jersey - Rahway, United States
R
USD 210K-331K Senior-level Full Time
Tasks
- Author and review regulatory documents
- Collaborate with translational clinical and biostatistics teams to integrate quantitative insights
- Develop and contribute to regulatory strategies
- Develop and implement integrated model informed drug development strategies
- Ensure alignment of modeling strategies with regulatory expectations
- Lead and mentor quantitative pharmacology team
- Lead quantitative pharmacology strategy across oncology programs to inform development decisions
- Provide scientific and operational oversight for deliverables
- Represent QP2 in cross functional governance forums
- Represent company in regulatory agency interactions and external collaborations
- Translate nonclinical findings into clinical development plans
Perks/Benefits
- 401k
- Comprehensive health insurance
- Dental insurance
- Paid Holidays
- Retirement benefits
- Vacation
- Vision insurance
Skills/Tech-stack
Biomarkers | Clinical Development | Clinical Pharmacology | Clinical Study Reporting | Clinical study | Dose selection | Drug development | Machine Learning | Model-informed drug development | Oncology drug development | Pharmacodynamics | Pharmacokinetics | Pharmacometrics | Regulatory Interactions | Regulatory strategy | Statistical modeling | Study reporting | Translational Pharmacokinetics | Translational Pharmacokinetics and Pharmacodynamics
Education
Roles
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