Exciting entry to mid level opportunity in NJ. Please contact me at [email protected]<mailto:[email protected]> for more info.
Responsibilities Develop, with support, pharmacometrics strategy and contribute to the clinical development plan, and perform model-informed drug discovery and development (MIDD) in clinical development projects Will provide pharmacometrics analyses (model based meta analysis, Nonlinear mixed effect models, dose optimization, etc)for internal decision making throughout clinical development and registration Ensures timely delivery of documents such as dataset specification, pharmacometric analysis plan, summary report Ensures timely delivery of documents such as protocols, submission documents, etc. Will represent pharmacometrics department on clinical development teams and other initiatives. Will manage projects with academic and CRO partners. Level is commensurate with experience. Must have a PhD in related field and 0 to 5 years experience. Hands on expertise with NONMEM and R is required. Additional expertise in software such as WinNonLIn, SAS, MATLAB, or SimCyp is also helpful. [cid:[email protected]] Brenda Roseberry Division Manager-Scientific Preclinical/Clinical--PK, Pharmacology, Pharmacometrics, Biomarkers, Bioanalysis 720-328-9526 - Office 315-415-4353 - Mobile 720-475-1176 - Fax [cid:[email protected]] <http://www.linkedin.com/profile/view?id=19937880&authType=name&authToken=b5d_>
