- 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.