Assistant CRA
Core
Support Clinical Research Associates (CRAs) and Study Clinical Leads with site preparedness, logistical support, remote monitoring, and document management across clinical trials.
Role type
Assistant Clinical Research Associate (IC)
Builds
Clinical trial operations and data integrity for pharmaceutical and biotech clients
Domain
Clinical Research / Life Sciences
Required skills
ICH GCP knowledge, medical terminology, document management, remote monitoring tools, vendor qualification, supply chain coordination, data reconciliation, MS Office proficiency
Preferred skills
English and Turkish language skills, basic medical/therapeutic area knowledge
Technologies
EMR/EHR, CTMS, centralized monitoring tools, 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 training and system access management; coordinate logistics for investigator meetings; manage study/site supply and vendor trackers; reconcile CRF, queries, deviations, and safety reports; follow up on missing study data (ECGs, lab samples, e-diaries).