Teams at PSI CRO

Supports clinical trial sites by coordinating documentation, supplies, payments, regulatory submissions, audits, training, safety communications, CTMS updates, vendor activities, and issue resolution. Maintains trial master files and investigator site files, tracks site and vendor deliverables, supports monitors, and serves as a primary communication contact for clinical research sites.

Supports clinical trial site management by coordinating documentation, supplies, payments, regulatory submissions, audits, training, safety information, CTMS updates, vendor activities, and communication with sites, monitors, and internal departments. Maintains trial master files and investigator site files, tracks site issues and action items, supports data and query completion, and ensures site and vendor requirements are completed accurately and on schedule.

Supports international clinical research projects by maintaining databases and tracking systems, managing documents, coordinating site and vendor communications, resolving site queries, arranging training and system access, administering payments, routing communications, and assisting with project meetings, agendas, and minutes. Requires strong organization, attention to detail, administrative capability, and business-level Thai, Japanese, and English communication, including JLPT N2 or equivalent Japanese stakeholder experience.