Teams at PSI CRO

Provide administrative and operational support for clinical trial sites: manage clinical supplies, regulatory/ethics submissions, TMF/ISF documentation, CTMS/EDC updates, vendor coordination, training, meeting organization, and site communication to ensure study compliance and timely data resolution.

The Principal Statistician will lead statistical activities for global clinical trials, oversee statistical analysis, and liaise with cross-functional teams on project-related inquiries.

Contribute to statistical activities for global clinical trials, performing analyses, developing protocols, leading teams, and ensuring quality standards are met.