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 for pharmaceutical and biotech clients
Domain
Life Sciences / Clinical Research
Deliverable
client delivery
Required skills
ICH GCP knowledge, medical terminology, document management, remote monitoring support, data reconciliation, system access management, supply chain coordination
Preferred skills
Registered Nursing certification, life science degree, experience with EMR/EHR systems
Technologies
MS Office, CTMS, electronic study data systems
Responsibilities
Complete study and site management activities per task matrix; perform remote review of EMR/EHR checklists; verify document collection and update site EDL; coordinate study/site supply management; reconcile CRF, queries, deviations, and safety reports; support site staff training and vendor qualification processes.
Seniority
Junior, 0-2 years experience