Experienced professional individual contributor that works under limited supervision applying subject matter knowledge in the area of Medical Affairs
Job Summary
Experienced professional individual contributor that works under limited supervision applying subject matter knowledge in the area of Medical Affairs.
Oversees the direction, planning, execution, clinical trials/research and data collection activities, contributing to implementation of clinical protocols and completion of final reports.
Responsible for directing human clinical trials, phases III & IV for company products under development, participating in adverse event reporting and safety responsibilities monitoring.
Matching Summary
Experienced professional individual contributor that works under limited supervision applying subject matter knowledge in the area of Medical Affairs.
Skills & Requirements
Must-have
Medical Affairs subject matter knowledge
clinical trials planning and execution
data collection activities oversight
adverse event reporting and monitoring
regulatory agency reporting coordination
Nice-to-have
consultant liaison with other corporations
investigator initiation and group studies oversight