Assistant CRA
Core
Support Clinical Research Associates with site preparedness, logistical monitoring, and administrative tasks to ensure compliance with regulatory guidelines.
Role type
Assistant Clinical Research Associate (IC)
Builds
Clinical trial operations and site management processes
Domain
Pharmaceutical/Biotech clinical research
Required skills
ICH GCP knowledge, medical terminology understanding, document verification, remote monitoring support, supply management, data reconciliation, system access management, translation review, vendor coordination
Preferred skills
Registered Nursing certification, life science degree, experience with EMR/EHR systems, familiarity with centralized monitoring tools
Technologies
MS Office, CTMS, electronic study data systems, centralized monitoring tools
Responsibilities
Complete study and site management activities per task matrix, verify document collection and RCR submission status, support remote review of EMR/EHR checklists, coordinate study/site supply management, perform reconciliation tasks on CRF and safety reports, maintain vendor trackers and essential documents
Seniority
Junior, 0-2 years experience