CRA (Level I or II) FSP - Athens
Core
Conduct remote and on-site clinical monitoring visits to assess protocol and regulatory compliance, manage site processes, and ensure data reliability for pharmaceutical and biotech clinical trials.
Role type
Junior Clinical Research Associate (IC)
Builds
Clinical trial data integrity and regulatory compliance for sponsors
Domain
Life Sciences / Clinical Research
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Risk-based monitoring, root cause analysis, critical thinking, problem-solving, data verification (SDR/SDV/CRF), investigator site initiation, trial close-out, ICH-GCP knowledge, medical terminology, regulatory compliance, travel management
Preferred skills
Registered Nursing certification, life sciences degree, experience in health sciences with medical training
Technologies
Clinical Trial Management Systems, Microsoft Office
Responsibilities
Monitor investigator sites using risk-based approaches to identify deficiencies and implement corrective actions; review essential documents and conduct on-site file reviews; track trial status and update study systems; facilitate communication between sites, clients, and internal teams; perform trial close-out and material retrieval; manage investigator payments and travel logistics.
Seniority
Junior, hands-on IC