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Preclinical ADME Lead - France  

Company managed [?] Still accepting applications

Posted on : 11 May 2017

Project Description

Description:
You will support the Development team in contributing to the characterization of preclinical ADME profile of new drug candidates.
 In particular, you will: 
  • Provide the scientific and technical expertise to drive the investigation of the ADME profile of drug candidates under development within the company
  •  Interface with CROs selected for preclinical in vivo and in vitro ADME studies (to discuss budgets, timelines, study plans, results and reports)
  • Ensure compliance with GLP requirements
  • Act as DMPK representative in project teams
  • Contribute to the selection of the best drug candidates
  • Contribute to the preparation of scientific and technical dossiers for regulatory purposes
  • Report to project teams and senior management.  
  


Requirements 
  • The successful candidate is a biologist, pharmacist or veterinarian with a Master or PhD Drug Metabolism and Pharmacokinetics and at least 10 years of experience in a relevant CRO or in the pharmaceutical industry.
  •  Knowledge of/experience with conduction of preclinical safety studies would be an asset.
  •  He (she) enjoys working in cross functional teams and has excellent oral and written communication skills as well as good command in English (writing and speaking).