Responsible for remote site monitoring activities to ensure sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor volume
May monitor and/or co-monitor on-site when needed
Performs Site Identification (Site ID) and/or Site Start-Up (SSU) activities as needed
Works collaboratively with other functional groups such as Clinical Operations Lead (COL), Project Management, Regulatory Start-Up (RSU), and Epidemiology
Completes appropriate therapeutic, protocol, and clinical research training to perform job duties.

2
3 years of prior relevant experience
Intermediate level knowledge of principles, theories, and concepts of a job area, typically obtained through advanced education combined with experience

Senior Site Manager

Key skills