Collaborate with preclinical and clinical departments to design and execute pharmacokinetic studies. Utilize quantitative pharmacology software to analyze, interpret, and model preclinical and clinical pharmacokinetic data, providing quantitative pharmacology support for R&D decision-making and clinical trial design.
Communicate with preclinical and clinical teams for literature research and combine the drug's mechanism of action for PK/PD study design and modeling, offering support for clinical research and data interpretation.
Responsible for writing and reviewing quantitative pharmacology content in regulatory submission documents, including PKPD, PPK, or PBPK.
Provide expert quantitative pharmacology advice for new project initiation and project evaluations.

Master's degree or higher in Quantitative Pharmacology, Pharmacokinetics, Clinical Pharmacology, or related field.
Familiar with quantitative pharmacology processes, clinical pharmacology, and bioanalytical study guidelines, capable of independently drafting study plans and reports, and proficient in data analysis software.
Over 2 years of experience in quantitative pharmacology research in innovative drugs, preferably with small molecules, having independently led projects.
Proficient with modeling and data analysis software such as NONMEM, WinNonlin.
Strong written English skills, with speaking and listening skills as a plus.
Good adaptability, stress management, optimism, and a strong sense of teamwork.