Senior CRA - Belgium
Core
Senior Clinical Research Associate conducting risk-based monitoring of investigator sites to ensure protocol compliance, data accuracy, and subject safety across clinical trials.
Role type
Senior Clinical Research Associate (CRA)
Builds
Clinical trial data integrity and regulatory compliance for pharmaceutical and biotech sponsors
Domain
Clinical Research / Life Sciences
Deliverable
client delivery
Required skills
Risk-based monitoring, root cause analysis, protocol compliance, ICH-GCP guidelines, site management, data review (SDR/SDV/CRF), investigator identification, audit response
Preferred skills
Medical/therapeutic area knowledge, presentation skills, process improvement
Technologies
Clinical Trial Management Systems (CTMS), Microsoft Office
Responsibilities
Monitor investigator sites using risk-based approach; ensure data accuracy through document and source data review; manage site initiation and close-out; respond to audits and inspections; track trial status and update study systems; facilitate communication between sites, clients, and project teams.
Seniority
Senior, hands-on IC
