Assistant CRA - FSP
Core
Provide support for site preparedness, logistical monitoring, and remote monitoring activities in clinical trials.
Role type
Assistant Clinical Research Associate (FSP)
Builds
Clinical trial monitoring and site management processes
Domain
Pharmaceutical/Biotech clinical research
Required skills
ICH GCP knowledge, medical terminology, document verification, remote monitoring, supply management, data reconciliation, system access management, translation review
Preferred skills
Oncology clinical trial experience
Technologies
EMR/EHR, CTMS, dashboards, MS Office
Responsibilities
Orient and train on study-specific systems, verify document collection and RCR submission status, perform remote review of EMR/EHR checklists, coordinate study/site supply management, support site payments and invoice reconciliation, perform reconciliation tasks on CRF and safety reports, maintain vendor trackers and essential documents.
Seniority
Junior, 0-2 years experience