(Sr) Clinical Research Associate - Client-dedicated (FSP) Netherlands
Core
Conduct remote and on-site clinical monitoring and site management to ensure protocol and regulatory compliance for pharmaceutical clinical trials.
Role type
Senior Clinical Research Associate (CRA)
Builds
Clinical trial data reliability and subject safety
Domain
Life Sciences / Clinical Research
Deliverable
physical/clinical work
Required skills
Clinical monitoring, Risk Based Monitoring (RBM), Root Cause Analysis (RCA), ICH-GCP compliance, Site initiation, Data review (SDR/SDV/CRF), Investigational product inventory
Preferred skills
Medical/therapeutic area knowledge, Critical thinking, Problem-solving, Team collaboration
Technologies
Clinical Trial Management Systems (CTMS), Microsoft Office
Responsibilities
Monitor investigator sites using risk-based approaches; Conduct on-site and remote monitoring visits; Ensure audit readiness and document compliance; Initiate and close out clinical trial sites; Track trial status and generate progress reports; Respond to regulatory audits and inspections.
Seniority
Senior, hands-on IC