Assistant CRA
Core
Support Clinical Research Associates (CRAs) 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, expense reporting
Preferred skills
None stated
Technologies
EMR/EHR, CTMS, MS Office
Responsibilities
Orient and train on study-specific systems; perform remote review of EMR/EHR checklists; verify document collection and RCR submission status; support site staff vendor qualification; coordinate study/site supply management; reconcile CRF, query status, deviations, and safety reports; maintain essential document collection in systems.
Seniority
Entry-level to Junior (1-2 years experience)