Study Physician

Jun 02, 2021View PDF

Responsibilities:

  • 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.

 

Qualifications:

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