Perform Medical Review of adverse event reports including but not limited to all serious, events of special interest.
Provide input to key internal safety documents, including Risk Management documents (RMPs), development and updates/maintenance of expectedness guides.
Provide support for investigator brochures, protocols, informed consents, final study reports, as appropriate.
M.D. degree & 5Y+ pharmacovigilance experience in drug development pharma/biotech industry.
Experience specific to hematology preferred.
Fluent in English, both verbal and written.