About this role

Oversee and manage RWE clinical studies and other clinical projects
Manage multi-functional study teams throughout the study or project from kick-off through close-out
Responsible for ensuring all functional areas study team members deliver in a timely manner, on budget and with high quality throughout the duration of the study
Assist in study resourcing needs with other functional areas
Work closely with the client and team to initiate study start-up and kick off
Monitor for potential issues and risks throughout the study

Bachelor’s Degree or above in a health science field, epidemiology, public health, pharmaceutical or medical device research, or related health science field
5 years real world evidence, clinical or business background in drug or device research/development, biotechnology, pharmaceutical or clinical research and/or combination of education & experience
Experience with real world evidence, drug development process and/or medical writing preferred
Experience in the oversight of Monitoring activities preferred

Project Manager II – Real World Evidence, Late Phase Research

About this role