(Sr) Clinical Research Associate - Client-dedicated FSP - Belgium
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 clients.
Role type
Senior Clinical Research Associate (Level I)
Builds
Clinical trial execution and site management for top 50 pharmaceutical companies and 750+ biotechs
Domain
Life Sciences / Clinical Research / Pharmaceutical
Deliverable
client delivery
Required skills
Risk-based monitoring, root cause analysis, critical thinking, problem-solving, ICH-GCP compliance, site initiation, trial close-out, data accuracy verification (SDR/SDV/CRF), investigator management
Preferred skills
Medical/therapeutic area knowledge, presentation skills, process improvement initiatives
Technologies
Clinical Trial Management Systems (CTMS), Microsoft Office
Responsibilities
Monitor investigator sites using risk-based approaches to identify failures and implement corrective actions; ensure data accuracy through on-site and remote monitoring; initiate and close out clinical trial sites; conduct on-site file reviews; respond to audits and inspections; facilitate communication between sites, clients, and project teams.
Seniority
Senior, hands-on IC