Preclinical ADME Lead

Job description

Ref: MEC 219

 

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).