Clinical Pharmacologist II

. Responsibilities: -In this role, you will work collaboratively and be responsible for the timely and efficient design, analysis, interpretation and reporting of clinical pharmacology studies for early and full clinical development programs.
-As necessary, you may also conduct analyses and report results from PK/PD, population PK and/or toxicokinetic studies.



Requirements:

-PharmD, PhD, or MD with formal pharmacokinetic training and/or 2+ years experience in design and analysis of PK studies.
-Training/experience in advanced pharmacokinetics (PK/PD and population PK modeling) clinical pharmacology, medicine and/or pharmacy with clinical and/or statistical perspective is a strong plus.
-Hands on experience in clinical trials management/study conduct and/or basic laboratory sciences are also desirable.
-Must have established computer skills with detailed knowledge of PK programs and analysis software (e.g. WinNonlin, ADAPT II, Kinetica, WinNonmix, SAS, etc), along with experience with scientific graphing and analysis software (Sigma plot, GraphPad, Instat, etc).
-Must have excellent written and verbal communication skills.


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