Teams at PSI CRO

Lead on-site monitoring activities for Phase II/III studies in Canada, including SIV/RMV/COV visits, CRF review, source data verification, query resolution, site management, regulatory submission support, feasibility, and audit/inspection preparation. Act as site and vendor contact and communicate study progress with internal teams.

Lead and manage all study startup activities in Japan, including site selection, regulatory/IRB submissions, contract and budget negotiation, CTMS tracking, team training and mentoring, and process improvement to ensure timely site activation.

Provide clinical sites with technical support for study technologies (MRI, nuclear medicine, radiology); design and implement study-related technology forms and manuals; coordinate imaging data collection and documentation; organize technical training; perform site initiation and technical visits; advise site monitors and communicate technical resource needs.