- Pfizer (Groton, CT)
- …plays an important role in understanding drug safety and efficacy. As a pharmacometrician , you will work with multidisciplinary teams where you will use quantitative ... methods to provide context on study results and answer team questions during clinical drug development. While your primary therapeutic area will include cardiovascular and metabolic diseases, you may have opportunities to work on projects outside these areas.… more
- AbbVie (North Chicago, IL)
- …and techniques in the field of PK/PD modeling. Act as a lead pharmacometrician in his/her area of expertise and critically evaluate relevant Pharmacometric, PK/PD, ... Clinical Pharmacology and regulatory advances and integrate this knowledge into Clinical Pharmacology strategy for research or development programs. Responsibilities: + Contribute to clinical development by supporting Phase 1-4 studies with data analysis,… more
- Pfizer (New York, NY)
- …+ With guidance, contribute to the development of the model informed drug development (MIDD) plans for an assigned project to optimize prospective studies, inform ... drug development strategy and project decision-making, in collaboration with partners, in particular, clinical pharmacology + Conduct and report quantitative analyses which integrate knowledge of pharmacokinetics, pharmacodynamics, patient characteristics, and… more
- Ascendis Pharma (Palo Alto, CA)
- …PhD or PharmD with 15+ years' experience as a Clinical Pharmacologist/ Pharmacometrician in the pharmaceutical industry or related field/experience. + Extensive ... experience in building a department from scratch, quantitative pharmacology analyses and pharmacometric modeling and simulation oversight + Knowledge of datacloud infrastructure, R, R-shiny, MATLAB, NONMEM, PBPK (gastroplus or Simcyp or open source) or similar… more
- AbbVie (North Chicago, IL)
- …analyses and visualizations in interaction with the clinical pharmacologist or pharmacometrician + Produce dynamic and static data visualizations to communicate ... quantitative analyses + Create documentation for regulatory filings + Participate in the development of standard SAS Macros. Qualifications + MS in Statistics, Computer Science or a related field with 0+ years of relevant experience. OR BS in Statistics,… more