Clinical Research Coordinator Team

The Clinical Research Coordinator Team (CRCT) carries through the compliant set-up of the clinical trial and oversees patient and study visit management, scheduling, and assists with general conduct of a clinical trial with PI oversight.

Clinical Research Coordinator Services

Trained and credentialed clinical research coordinators that assist with patient recruitment, patient and study visit management, scheduling, orders development, facilitating monitoring visits, communication with campus and sponsor contacts and ensuring protocol and regulatory compliance during the conduct and closeout of a project.

Data Management Services

CRF and eCRF data transcription from medical record and source documents
Query resolution
Source Document Verification – a review of the source document templates against the protocol and CRF to assist with protocol-compliant data collection during study visits

Budget and Contract Management

Contract Office (CTC-SR, TDG, or OCGA) document submission for amendments
OnCore patient management to facilitate sponsor invoicing
Manage budget amendments