Assistant CRA FSP - Türkiye
Core
Support site preparedness, logistical monitoring, and site management for clinical trials in accordance with SOPs and regulatory guidelines.
Role type
Assistant Clinical Research Associate (FSP)
Builds
Clinical trial site management and monitoring support
Domain
Pharmaceutical/Biotech clinical research
Deliverable
client delivery
Required skills
ICH GCP knowledge, medical terminology understanding, document verification, remote monitoring support, supply management, data reconciliation, system access management, translation review
Preferred skills
Vendor qualification support, essential document collection, site payment coordination, safety report tracking
Technologies
EMR/EHR, CTMS, centralized monitoring tools, MS Office
Responsibilities
Orient and train on study-specific systems, verify document collection and RCR submission status, review patient-facing materials and translations, coordinate study/site supply management, perform reconciliation tasks on CRF and safety reports, support site staff training and vendor qualification processes
Seniority
Junior, 0-2 years experience