Description
The role performs routine in vitro ADME assays, develops and optimizes LC-MS/MS and complementary analytical methods, supports assay development and validation, analyzes experimental data, prepares reports, coordinates third-party pharmacokinetic studies, and presents results. It requires a Master's in Lifescience, at least 7 years of experience with LC-MS/MS, HPLC, and bioanalytical studies, practical biotechnology laboratory experience, strong scientific judgment, and the ability to collaborate across multidisciplinary drug discovery teams.
