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_