Google Cloud PlatformGCPGoogle CloudCommunicationTime Management
About this role
Role Overview
Execute clinical monitoring activities at clinical trial sites
Collaborate closely with Country and Regional Clinical Study Teams
Conduct onsite/remote pre-study, initiation, routine monitoring and closeout visits
Manage sites and site performance by tracking regulatory submissions
Ensure inspection readiness of the study and sites
Mentor junior staff
Requirements
BS in a scientific or healthcare discipline preferred
At least 3
5 years of monitoring experience
Advanced knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP), International Conference on Harmonization (ICH) guidelines
Excellent communication and interpersonal skills
Effective time management skills
Must be fluent in English and Italian
Efficient in Microsoft Word, Excel, PowerPoint, Outlook