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- #INTRODUCTORY NONMEM WORKSHOP UNIVERSITY AT BUFFALO SOFTWARE#
- #INTRODUCTORY NONMEM WORKSHOP UNIVERSITY AT BUFFALO TRIAL#
#INTRODUCTORY NONMEM WORKSHOP UNIVERSITY AT BUFFALO SOFTWARE#
Develop test and qualify software for the department. Analyze clinical pharmacokinetic, pharmacodynamic and safety data. Supervise monitoring staff, review safety data, oversee clinical data handling. Design, write, place and implement clinical trials. Prepare regulatory documentationĬlinical Research Scientist – Department of Clinical Pharmacology Arrange and conduct investigator meetings. Supervise monitoring staff, oversee clinical data handling. Write, place and implement clinical trials. Prepare and present regulatory documentation including IND, IDB, NDA, PLA, and Package Inserts. Deliver presentations at professional meetings, investigator meetings, and regulatory authority meetings. Train and manage scientific staff (MS and BS level). Test and qualify software for the department. Develop user-friendly tools to facilitate modeling analysis. Design and write clinical pharmacokinetics and pharmacodynamics aspects of clinical trials. Work with multidisciplinary teams to develop strategies for conducting rapid drug development programs. Develop and review functional specifications documents to support software qualificationĪssistant Director – Clinical Pharmacokinetics DMPK
#INTRODUCTORY NONMEM WORKSHOP UNIVERSITY AT BUFFALO TRIAL#
Work with the Scientific Advisory Board and the engineers to develop, test, and document software for the simulation of clinical trial designs. Scientific Advisory Group – Clinical Trial Simulation Teaching assistance for College of Medicineħ/99-11/01 Pharsight Corporation Scientific Advisory Group Design, analyze and report on clinical PK and PD analysis from clinical trials. Provide technical and educational assistance to industry on clinical trial analysis and simulation through CDDS programs. Research Topic: Synthesis of Novel Beta Lactam AntibioticsĬonsulting company for conducting PK and PK/PD analysis, Population based analysis and clinical trial simulation following GCP (Good Clinical Practices) and nonclinical GLP (where applicable) analysisĩ/00-3/02 Georgetown University Center for Drug Development ScienceĪssociate Professor – Dept of Pharmacology Stevens Institute of Technology, Hoboken, N.J. The Oral and IV Pharmacokinetics of Ethyl Alcohol in the Fed and Fasted States Using the Dog Model. The Ohio State University – College of Pharmacy Columbus, Ohio 43210 Degree in Pharmaceutics and Pharmaceutical Chemistry (703) Position and Affiliation: President Projections Research, Inc.įields and Areas of Specialization: Pharmacokinetics, pharmacodynamics, pharmacometrics, clinical trial designġ2/89: Ph.D.