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


1 Rue Jeanne d’Arc 57160 Rozérieulles

06 42 63 28 06