Position Description: In this role, you will lead the design, analysis, interpretation and reporting of pharmacokinetic, pharmacodynamic, drug disposition, and drug metabolism data from clinical studies for compounds in Oncology diseases utilizing state of the art technology in support of clinical development plans. You will perform pharmacokinetic and pharmacodynamic modeling, contribute to Clinical Pharmacology related regulatory documents and draft relevant sections in support of clinical development plans, and provide Clinical Pharmacology perspective on cross functional teams. You will also participate in regulatory interactions as needed as well as evaluate feasibility of clinical studies and provide input to the design and review of clinical protocols. In addition, you must be at the forefront of scientific literature in the areas of drug metabolism, pharmacokinetics/pharmacodynamics and clinical pharmacology.
Position Requirements: Requirements for this position include a Ph.D. or a PharmD with a postdoctoral fellowship in Pharmacokinetics, Biopharmaceutics or a related field with a minimum of 1-5 years experience in pharmacokinetic, pharmacodynamic and drug metabolism techniques; industry experience is preferred.
Direct experience designing, conducting and interpreting studies in population PK, PK/PD correlations, modeling and simulation utilizing standard modeling software (NONMEM, ADAPT-II, R/S-Plus, WinNonlin, etc.) and their application to the drug development is higly desired.
Candidate must display strong written and oral communication skills necessary to deliver scientific presentations.
The ability to work in a dynamic team oriented environment as demonstrated by participating in and contributing to cross functional teams is necessary.
Experience in building an internal network of collaborators is desired.
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