Know well about bioanalytical method development using LC-MS/MS
Experiences on conducting bioanalysis work for PK samples and in vitro ADME samples
Working together with CRO to perform PK parameter calculation using WinNonlin software and finalize the study report
Communicate with supervisor/CRO about study design, operation, progress and issues
Peer review CRO's data report and analysis the results
Acting as a project DMPK lead scientist/investigator and ensure every DMPK report is delivered error-free and in timely fashion to support our company projects moving forward smoothly and quickly
Others assigned if needed
Requirements:
MS in Analytical chemistry, Pharmaceutical Science or Pharmacology related