Responsible for assisting with early drug discovery and preclinical/clinical regulatory submission phases, including in vitro and in vivo drug metabolism studies.
Provide suggestions and support for formulation selection and solvent screening during early research, based on molecular and target characteristics.
Manage the preparation, review, and confirmation of pharmacokinetic documentation during regulatory submissions.
Address technical challenges, analyze potential project risks, and provide ADME/PK scientific support.

Master's degree or higher in Pharmacy, Pharmaceutical Analysis, Analytical Chemistry, Pharmacokinetics, or related fields. Familiarity with analysis software such as WinNonlin.
Over five years of experience in drug metabolism research, with a proven track record of advancing projects to clinical trials or market. Experience in small molecule drug development is highly valued.
Knowledge of the new drug development process, understanding the interconnections between pharmacokinetics, pharmacodynamics, toxicology, and clinical studies. Ability to integrate R&D stages and facilitate systemic evaluations for drug development.
A proactive, dedicated professional with excellent communication skills and a strong team spirit.