Clinical Research Associates

Monitoring activities
Setting up trial logistics (drafting procedures, creating trial documents, organizing various circuits: patient, therapeutic units)
Feasibility/selection visit
Site initiation visits
Monitoring visits
Close out visits
Remote monitoring for all types of visit
Recruitment follow-up and reminders

Coordination activities
Lead CRA / Coordination of CRA monitors: centralization of reports, e-CRF consistency, report validation, sponsor transfer
Investigator research
Budget trial evaluation
Study follow-up strategy (follow-up tables : SAEs, patient progress, e-CRF completion etc…)

Quality assurance procedures
Help with preparing, carrying out and following up audit visits
Help in preparing, carrying out and following up inspection visits

Logistics organization for patient transport
Individual management of patient travel to investigational sites
Partnership with a dedicated company
Invoicing guarantee anonimized
