CRA I - FSP - Paris region
Core
Conduct remote and on-site clinical monitoring to ensure protocol and regulatory compliance, manage site processes, and guarantee data reliability for pharmaceutical and biotech sponsors.
Role type
Junior Clinical Research Associate (CRA I)
Builds
Clinical trial monitoring activities and site management deliverables
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), investigational product inventory, regulatory compliance (ICH-GCP), site initiation, trial close-out, document management
Preferred skills
Medical/therapeutic area knowledge, clinical trial management systems proficiency
Technologies
Clinical Trial Management Systems, Microsoft Office
Responsibilities
Monitor investigator sites using risk-based approaches to identify and resolve compliance issues; verify data accuracy through on-site and remote activities; initiate and close out clinical trial sites; conduct on-site file reviews; track trial status and provide progress reports; facilitate communication between sites, clients, and internal teams.
Seniority
Junior, hands-on IC