Study Physician

Jan 11, 2022View PDF


  • Manage global or regional studies and involve in the design, conduct, monitoring, data interpretation and reporting of individual clinical trials.
  • Provide expert scientific and clinical input to Clinical Development, Regulatory Affairs, Biostatistics, Data Management, and other related departments.
  • As a trial level physician and medical monitor for clinical studies.


  • D. degree & 2Y+ industry drug development experience.
  • Experience specific to oncology preferred.
  • Fluent in English, both verbal and written.