Assistant CRA
Core
Support Clinical Research Associates with site preparedness, logistical monitoring, and administrative tasks to ensure study compliance and data integrity.
Role type
Assistant Clinical Research Associate (IC)
Builds
Clinical trials 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 administration
Preferred skills
Registered Nursing certification, life science degree, English fluency
Technologies
EMR/EHR, CTMS, MS Office
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