Roberta Longo

Background

About Roberta Longo

Clinical Operations Leader with more than 18 years of experience in phase clinical trial studies in various indications working in CROs. Broad background in clinical trials management and very extensive monitoring experience, including coordination and performing clinical on-site monitoring activities, collecting regulatory documentation, performing feasibility, qualification, initiation, monitoring and termination of investigational-sites. Experience on a large study as regional COL and also gained experience in GCOL role (phase II, studies).Strong communication and leadership skills, leading European and global team, effectively communicating with internal and external customers as well as third party vendors. Skilled in Electronic Data Capture (EDC), Medidata, Oncology, Clinical Data Management, and Clinical Monitoring. Strong research professional graduated from Università LIUC di Castellanza (VA).