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