Sr CRA - FSP - Belgium & Netherlands
Core
Senior Clinical Research Associate conducting risk-based monitoring, site management, and regulatory compliance for pharmaceutical clinical trials.
Role type
Senior IC clinical research associate (monitoring)
Builds
Clinical trial data integrity and regulatory compliance for pharma/biotech 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, protocol compliance, ICH-GCP guidelines, site initiation, data review (SDR/SDV/CRF), investigator management, audit readiness
Preferred skills
Medical/therapeutic area knowledge, problem-solving, travel adaptability
Technologies
Clinical Trial Management Systems (CTMS), Microsoft Office
Responsibilities
Monitor investigator sites for compliance and data accuracy, initiate and manage clinical trial sites, ensure audit readiness and document management, track trial status and progress, facilitate communication between sites and sponsors
Seniority
Senior, hands-on IC