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Research - Principal Investigator (DOE), Clinical Pharmacokinetics - United States  

Company managed [?] Still accepting applications

Posted on : 13 May 2017

Project Description

This position will be responsible for performing PK/PD analysis, population PK/PD analysis, and PBPK for Biologics and small molecules in the clinical pharmacokinetics group.

Job Responsibilities

  • Advise clinical teams on PK and PK/PD study design
  • Perform PK/PD analyses, pop PK/PD analyses, interpret and report data to clinical teams and management in a timely manner
  • Conduct model based simulations using PBPK method to design studies that yield high value PK/PD information for future critical decisions
  • Represent clinical pharmacokinetics on clinical project teams
  • Work with clinician, biostatistician, and data manager to provide deliverables on time
  • Present work at internal and external scientific meetings and publish manuscripts in peer-reviewed journals

Minimum Requirements 

  • Ph.D. in Pharmacokinetics, Pharmacometrics, Pharmacology, Engineering, Statistics or related fields
  • 1+ years of experience in clinical PK, population PK analysis and PBPK modeling
  • Experience in analyzing clinical pharmacology data
  • Experience in large molecule development is highly preferable
  • Experience with a range of software packages, such as but not limited to: WinNonlin, NONMEM, R, SimCyp and GastroPlus
  • Experience with writing reports for regulatory submissions is desired
  • Excellent written and verbal communication skills
  • Ability to work independently