Teams at Premier Research

Process, verify, and approve investigator/site invoices for clinical trials; track invoice statuses and individual workload in Excel; query and escalate anomalies; provide standard and ad-hoc reports; obtain necessary approvals and support monthly workload metrics.

As a Principal Biostatistical Programmer, you will develop SAS programs for clinical trials, perform quality control, generate analysis datasets, and lead interactions with study teams.

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.