Jesse R. Boado Email & Phone Number

Newark, CA

• Assist in preparation and reproduction of study materials during study start-up phase of clinical trials
• Schedule logistical and technical trainings with site personnel
• Maintaining regulatory documentation including pre-trial questionnaires, eligibility reports, and authorization letters
• Manage site communications, generate site and patient reports and queries, and verify reports prior to distribution to clinical sites and sponsors

Newark, CA

• Collect and receive patient data/subject documentation on transmittal forms
• Receipt and Data entry multiple records/demographics into secured servers
• Process Imaging modalities (CT scans, MRI, Angiograms) for labeling needs