Our skilled and well-trained clinical research associates (CRAs) ensure the highest quality data review and effective interaction with study sites. Our CRAs conduct on-site monitoring visits throughout the study to:
- oversee data collection and recording;
- review source documentation and case report forms;
- ensure regulatory compliance;
- resolve data queries;
- conduct interim analyses as requested by customers; and
- set-up a data safety monitoring board (DSMB).