Assistant CRA - FSP - Paris region
Core
Provide logistical and administrative support to Clinical Research Associates (CRAs) for site management, remote monitoring, and study supply coordination across clinical trials.
Role type
Assistant Clinical Research Associate (FSP)
Builds
Clinical trial site management and remote monitoring support
Domain
Pharmaceutical/Biotech clinical research
Deliverable
client delivery
Required skills
ICH GCP knowledge, medical terminology understanding, document verification, supply chain coordination, data reconciliation, system access management, translation review
Preferred skills
Vendor qualification support, essential document collection, site payment coordination, root cause analysis
Technologies
EMR/EHR, CTMS, dashboards, MS Office
Responsibilities
Complete study and site management activities per task matrix; verify document collection and RCR submission status; coordinate study/site supply management; support remote review of centralized monitoring tools; perform reconciliation tasks on CRF, queries, deviations, and safety reports; maintain vendor trackers and essential document systems.
Seniority
Entry-level (0-2 years experience)