Teams at Premier Research

Coordinate and facilitate clinical trial activities at site ensuring compliance with protocol, GCP, and local regulations. Support the Principal Investigator and site team, perform timely CRF/eCRF data entry, maintain clinical trial documentation including the Trial Master File, review site processes, identify gaps, and support process roll-out to ensure patient safety and data accuracy.

The Site Solutions Executive coordinates clinical trial activities, ensures compliance with protocols, and supports the research team with data entry and documentation.

Coordinate and facilitate on-site clinical trial activities ensuring compliance with protocol, GCP, and local regulations. Support the Principal Investigator and site team with data entry, TMF maintenance, regulatory/ethics submissions, patient scheduling and enrollment, samples logistics, site monitoring visits, and site performance reporting. Build and maintain potential patient databases and support community/patient-awareness events.